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By N. Verbaan, E. Bourricaudy, M. Dry

"Starfield Resources is developing a novel circuit for the recovery of nickel, copper, cobalt, iron oxide, sulphuric acid and precious metals from the Ferguson Lake deposit in Nunavut, Canada. In this deposit, pentlandite is too finely disseminated in pyrrhotite for the production of a smelter-grade nickel concentrate at an acceptable nickel recovery, so established technology is not applicable and a novel chloride-based circuit is under development. The enabling aspect of this circuit is the hydrolysis of ferric chloride to hematite, releasing gaseous hydrochloric acid that is recycled. Conventional steps are used for separating and recovering the valuable metals from the chloride solution generated. This paper briefly outlines the circuit and presents the results of experimental work on the enabling steps, viz. the oxidation and hydrolysis of iron chloride to hematite and gaseous hydrochloric acid.IntroductionThe Ferguson Lake bulk sulphide ore body in Nunavut, Canada, owned by Starfield Resources Inc., contains significant amounts of base and precious metals but its mineralogy is such that it is not amenable to conventional processing. Pentlandite, for example, is too finely disseminated in pyrhhotite for even modem techniques such as fine grinding and improved flotation reagents to be effective [ 1] and extracting the value requires processing the entire bulk sulphide, including the pyrrhotite. To give the project a total green footprint, in terms of both carbon emissions and acid rock drainage, Starfield imposed the following requirements:• No reactive tailings to generate acid rock drainage.• No gaseous emissions other than normal atmospheric constituents.• No liquid effluents.• No regular consumption of fossil fuel.• High recoveries of all the valuable metals."

Jan 1, 2011

By Kanchan Mondal

"Methanol, lower hydrocarbons, CO, and HCOOH formation have been by the reduction of CO2 with H2. Un-catalyzed electro-reduction requires a significant overvoltage. An alternate route has been conceptualized. Production of hydrogen from water can be achieved by chemical oxidation of a metal in water followed by oxidation of the hydronium ion by the released electrons to form hydrogen radical. It is hypothesized that circumventing the problem of the formation of hydrogen molecule is essential while having the hydrogen radical to react with CO2 forming methanol, etc. This may be possible by a bimetallic catalyst acting as a galvanic couple, wherein one metal acts as the electron donor for the production of hydrogen radical while the other acts as a catalyst for the reduction of CO2. This may enhance the reaction rates. The current concept circumvents the need for an external electric field unlike the electrochemical process.IntroductionUtilization of carbon dioxide as a raw material, not only as carbon sources but also as useful chemical feedstock is a more holistic approach to reduce air pollution by flue gases (1-3). Several methods have been proposed to maintain the concentration of atmospheric CO2 or to reduce and recycle it. One of these is the chemical fixations using catalysts. The conversion of CO2 to methanol by hydrogenation over copper containing catalysts is one of the most widely studied subjects in this area. The limitation in this reaction is the low conversion of CO2."

Jan 1, 2008

By K. O. Fagerlund

Theoretically and experimentally determined copper matte settling rate in iron silicate slag has been discussed. Separation and settling rate measurements of sand, homogenised slag and 25%Cu concentrate, 63%Cu industrial, and 71%Cu synthetic copper mattes were carried out by mixing crushed slag and matte samples with silica sand in an alumina crucible and melting at 1300-1350°C. Two different types of slag compositions were employed, with Fe/SiO2-ratio 1.4 and 1.7. The separation rate was followed by taking samples from the .melt. As expected, the settling rate of copper matte in fayalite slag depended on the slag composition, where the increasing silica decreased the matte settling rate. Microanalysis of solidified slags showed that the rate of separation of low grade matte was low compared with high grade matte and the presence of a very small size fraction of matte droplets in slag remained unsettled in stagnant fluid. The production of sulfur dioxide gas inside the molten bath was found to be possible up to a certain iron sulfide content in the matte. Also, copper matte settling rates in industrial furnaces have been discussed.

Jan 1, 1999

By Andy Judge

"In traditional Permanent Magnet Machines, such as electric motors and generators, power is transmitted by magnetic flux passing through an air gap, which has a very low magnetic permeability, limiting performance. However, reducing the air gap through traditional means carries risks in manufacturing, with tight tolerances and associated costs, and reliability, with thermal and dynamic effects requiring adequate clearance. Using a magnetically permeable, high thermal conductivity material has the potential to improve magnetic performance, while at the same time offering performance advantages in heat transfer.Ferrofluids can be used to improve permeability in the rotor I stator gap. However, there are several tradeoffs in this approach. Fluid immersion comes with an increase in fluid friction loss compared to the windage losses of a traditional system. Isolating the rotating components from the ferrofluid can offset this effect. Also, while the magnetic effect can be positive for gap permeability, leakage flux can increase, and saturation can limit gains. These effects must be taken into account for a system optimized for ferrofluid immersion.IntroductionPermanent Magnet Machines (PMM's) convert electrical energy to mechanical energy in motor applications, or, for generator applications, convert mechanical energy to electrical energy through means of passing alternately polarized magnets past electrical coils. Looking at a simplified version of a PMM, where Rx is magnetic reluctance and <l>x is magnetic flux, we have the circuit shown in Figure 1."

Jan 1, 2013

Plastics recycling has become an established national industry in Korea. However, it is still in its infant stage and experiences growing pains. In Korea, mixed plastic wastes generated from households after hand picking and/or mechanical sorting processes amount to 1,700,000 ton per year in 2005, and most of these waste are finally end up with landfill and/or incineration due to lacks of separation technologies and economical reasons. These plastic wastes can not be used as raw materials for chemical and/or thermal recycling because of their high content of PVC (upto 4.0 wt.%). In the present work, gravity separation system has been developed to remove PVC from the mixed plastic waste and recover the individual plastics. The separation system mainly consists of air classification, crushing, feeding system at fixed rate and wet-type gravity separation system. The gravity system based on centrifugal separation also consists of mixing, precleaning, separation, dewatering, recovery system, wastewater treatment system, etc. The main objective of this process to be developed is to achieve high separation efficiency of polyolefins (PE, PP, PS) with less than 0.3 wt.% PVC content and less than 10% moisture content in the final products. The system with a capacity of 0.5 ton per hour is developed and operational results are presented.

Jan 1, 2006

By Tejs Vegge

The lack of suitable means of storing hydrogen for use in the transport sector is generally viewed as a primary showstopper for a hydrogen economy. Recent developments within solid state hydrogen storage in complex hydrides and metal ammines have sparked new hope of a long term solution, but as of now, no materials fulfill all the DoE targets for onboard storage [1]. A detailed physical understanding of the ab-/desorption processes and the role of the essential catalytic additives is an essential prerequisite for the development of new optimized hydrogen storage systems. Here, we illustrate the potential of utilizing the synergy of combining state-of-the-art in theoretical methods and experimental techniques in the analysis and design of materials for hydrogen storage. Recent advances in computer hard- and software has made it possible to treat many of the essential problems in such materials, i.e. structural stability, hydrogen dissociation and diffusion, with high accuracy methods like density functional theory. We rely on such results to guide our synthesis of new materials, and to interpret our experimental results from, e.g. time dependant in situ x-ray diffraction, synchrotron/neutron experiments, and advanced materials testing. Through a continuous feed-back optimization loop between theory and experiments, the obtained nano-scale insight is used to expedite the design and development of novel materials for hydrogen storage.

Jan 1, 2006

By Rikiya Kamezawa, Rudiono, Manabu Takeuchi

"Schottky type solar cells based on phthalocyanine (Pc) thin films were fabricated, and their photovoltaic performance was investigated in various ambient atmospheres. Most of cells prepared in this study showed a good rectification and photovoltaic effects in the visible wavelength region. The introduction ofN02 gas into the measuring chamber was confirmed to increase the current both in dark and under light illumination. However, chemical reaction between the Al electrode and N02 formed some oxide and deteriorated the Schottky barrier, resulting in an increase in cell resistivity. SF 6 gas also showed similar effects on the cell performance.IntroductionPhthalocyanine is one of the typical organic semiconductors, which shows high photoconductive sensitivity in the visible to infrared region. Today, several kinds of metal phthalocyanines are used in electrophotographic photoreceptors. In addition, application of phthalocyanines to solar cells have also been trying by many workers [1, 2]. Many efforts have been made for improving performance of phthalocyanine solar cells by modification of device structure [3, 4], doping by dye or pigment [5, 6] and incorporation of metal clusters [7]. It is known that electrical conductivity in phthalocyanine is increased by adsorption ofNO2 [8, 9]. We tried to improve photovoltaic performance ofphthalocyanine solar cell by adsorption ofNO2. This paper describes the influence of N02 adsorption on the photovoltaic behavior of phthalocyanine solar cells."

Jan 1, 2000

By K. Asokan, K. Subramanian

"Electrowinning of copper by monopolar cells require common anode and cathode busbar and crossbars to connect each electrode to the respective common busbar. On the other hand, the bipolar configuration warrants the end electrodes only to be connected to busbars; there is substantial reduction in copper requirement. In the present work, an electrowinning cell with bipolar electrodes and end electrodes, each having an area of 1000 cm2 was designed and operated. The bipolar electrode is made of mixed metal oxide coated titanium mesh welded to plain titanium sheet. Coated titanium mesh acts as anode and the plain titanium sheet acts as cathode. Environmentally unacceptable lead anode and the recurring loss of lead are done away with. Closer spacing of the electrodes, paves way for the application of higher current density leading to mass transfer enhancement. Performance of bipolar copper electrowinning cell is reported.1. IntroductionThe normally adopted practice in electrowinning of copper is the conventional monopolar configuration. In this practice, the individual electrodes act either as anode or cathode. Hence there is a need to connect every one of the electrodes to the common anode or cathode busbar and crossbars running across the top of the cell are necessary. The common busbar carries very high current which is divided among the individual crossbars and hence has to be thicker in relation to the current load of the cell. The drawback of the need to use common busbars of thicker cross section and the need to have crossbars are obviated in the bipolar configuration."

Jan 1, 2009

By Xiaohui Li, Lianyun Liu, Hongmin Zhu, Chunfang Zi, Kai Huang, Hongjie Li

"The dissolution kinetics of steelmaking slag in pure water was studied, and the relative influential factors were investigated. The dissolution behavior of slag particles in water was well described by Noyes–Whitney equation, and for this kind of sparingly soluble rigid mineral this simple model was extensively applicable to describe their dissolution process. Experimental data were also obtained to confirm the significant promotion effect on the growth of some algae.1 . IntroductionIt has been found that the population of phytoplankton distributed in the ocean was significantly related to the concentration of some elements [1]. For example, silicon and iron were very low in the high-nitrate low-chlorophyll (HNLC) areas, which was the main factor limiting phytoplankton and other biomass growth in these open ocean surface water [7]. The silicon and iron-rich test also confirmed that the supply of these elements had the direct effect on the growth of phytoplankton processes at HNLC areas [2-8]. So in order to promote the growth of phytoplankton in these ocean areas, providing some of these elements into these ocean areas is a natural idea for choice. Steelmaking slag is a good resource for consideration because it usually contains silicon, iron, phosphorus and other elements that are necessary for the growth of phytoplankton [8-10].Haraguchi has proposed the following idea that [5-6], if steelmaking slag can be spread to the open ocean, the trace components like silicate, iron and phosphate as the indispensable nutrients for the growth of phytoplankton, will be leached into the sea water, not only promoting the growth of phytoplankton, but also making good use of these huge amount of steelmaking slag produced every year. Based on this idea, they have carried out studies in recent years and they found that silicon and iron in the slag could be extracted into seawater effectively and play a positive role in the growth process of many algae. About the dissolution of the steelmaking slag, the Japanese scholars' research work mainly focused on the thermodynamic analysis of its dissolution possibility, and in the process of dissolution they tried to adjust the pH value of the seawater by continuously adding hydrochloric acid, which was deviated from the natural conditions of dissolution, and so the laws drawn under these special conditions can not give the identical guide to the practical application. Therefore, it is quite necessary to investigate the dissolution behavior of the steelmaking slag in the seawater at the normal pH range without adjustment to simulate the dissolution possibility under the natural conditions. In the present study, the silicon extraction behavior from the steelmaking slag was investigated and the dissolution kinetics in this process was also discussed in detail. Further studies were also performed here to evaluate the promotion of steelmaking slag on the growth of algae."

Jan 1, 2011

By Gerald Onyedika, Tochi Onwumere, Martin Ogwuegbu

"The kinetic study for the leaching of iron from cassiterite ore in KOH solution was studied. The effects of KOH concentration, particle size and reaction temperature on the leaching rate of iron were also examined. The results of leaching studies showed that the leaching of iron from cassiterite ore in KOH solution is significantly influenced by the reaction temperature, KOH concentration, and decrease in particle size. The study showed that 90.62% of iron ore was leached in 8M KOH solution at 80°C within 120 minutes. The experimental data were well evaluated using the shrinking model for surface chemical reaction and diffusion control through the product layer. The activation energies for the iron ore dissolution using the two models were calculated to be 32.06KJmor1 and 97.97 KJmor' respectively.IntroductionIn recent times, there has been increasing attention on the kinetic study of mineral dissolution. In most of these studies, the experimental results were analyzed with a suitable shrinking core model under the assumption that the ore is a homogeneous spherical solid phase [1-4]. A study of the dissolution kinetics of a Nigerian cassiterite ore by hydrochloric acid showed that increase in the hydrochloric acid concentration is accompanied with increase in the amount of cassiterite ore dissolved at various times [4]. The optimal concentration was found to be 4.0M HCl, after which there was a decline in the amount of the ore dissolved, which showed that the concentration of the reagent has a significant effect on the leaching rate of the ore. Also in studying the effect of stirring speed on the rate of cassiterite ore dissolution while keeping other conditions constant for 120 minutes, the result showed that the rate of cassiterite ore dissolution was dependent on the stirring speed over a range of 0 to 630 rpm. Above 360 rpm, the stirring speed no longer had any effect on the solid dissolution. The dissolution rates of cassiterite were analyzed using a suitable shrinking model. The results showed that the reaction was controlled by the diffusion of tin through the porous product layer, a reaction order with respect to hydrogen ion concentration of 0.92 M and activation energy of 50.05KJmor'. In another kinetic study on the leaching of a low grade niobium-tantalum ore with concentrated KOH solution the effect ofreaction temperature, KOH concentration, agitation speed, particle size and alkali-to-ore mass ratio on the dissolution rate of niobium were examined [5]. The result of niobium leaching from low grade niobium-tantalum ore with concentrated KOH, solution at different agitation speeds showed that the dissolution rate increased with increase in agitation rate. In the case of particle size effect, the results show that small particles require much shorter time for complete dissolution than the large ones."

Jan 1, 2013

By Cao rong-jiang, Tang Xin-he

"In ordinary manufacture process of tungsten powder, a preferable intermediate product used is ammonium paratungstate (APT). The particle size of tungten powder made from it through W2OO58 is larger than 1. 0 um. In order to obtain ultrafine tungsten powder with narrow size distribution, a new type of tungstate, hydraziniull tungstate, was studied. Its formula is 5(N2H5)2O·12 WO.s , with tetragonal crystal structure of a=5.821 , c=18. 468. Three methods for preparing hydrazinium tungstate (ART) were set up and ART can be produced by current industrial APT process with little modification of operation and without any change of equipment.Under certain PH and operation condition of the solution from which ART was produced, an autoreduction of tungsten occured, which produced a lower valency tungstate with blue color when ART was heated at different temperatures, in N atmosphere, tungsten bronze, tetragonal W0290 and W02.7E could be obtained respectively. They all have the superiorities, in the production of tungsten powder, of superfine size and narrow size distribution [average size of 0.5um or even smaller.The rate of autoreduction of ART is very fast at elevated temperature. The reduction reaction, which gaves tetragonal WO290, could be handled smoothly without explosion. To research their behaviors at autoreduction temperatures and the products of autoreduction will be new advances of tungsten chemistry and may also serve tungsten industry with new processes and materials."

Jan 1, 1988

By A. Ohno

"A new near net shape casting process, OHNO Continuous Casting (OCC), has been recently developed. In this process, molten metal is fed into a heated mold maintained at a temperature above the solidification temperature of the metal being cast. Solidification begins from the central core of the casting rather than the wall of the mold. With the heated mold, the formation of crystals on the mold wall is prevented and solidification occurs out of contact with the mold surface. This produces near net shaped products with smooth, mirror-like surfaces and unidirectional grain structures free from cavities, porosity and segregation. Any crystals formed at the beginning of solidification decrease in number as solidification progresses and eventually a single crystal product is obtained. This process is applicable to any metal alloys, converting them into new materials with superior properties and quality.IntroductionAs a result of growing technical demands for more advanced and diversified materials, the OHNO Continuous Casting (OCC) technology has found many new applications in industry. Considerable interest in the process has been shown in Japan and other countries because of its distinct ability to:produce a single crystal, (1)produce a remarkably clean cast surface without a witness mark,provide extremely good ductility,and reduce casting defects and segregation.This paper provides an overview of the principle of the OCC process and describes the remarkable characteristics of the material produced by this method."

Jan 1, 1988

Today’s world relies upon advanced green technologies that are made of critical elements with unique properties. Examples include rare earth elements (REEs) that are critical in the manufacturing of wind turbines and electric/hybrid vehicle batteries, key components of a greener future that face supply uncertainty and near zero recycling. To tackle their supply challenges, activities have begun for urban mining from waste electrical and electronic equipment (WEEE) that contain considerable amount of REEs, but their current level of recycling is less than 1%. Current recycling practices use either pyrometallurgy, which is energy intensive, or hydrometallurgy that utilizes large volumes of acids and solvents and generates large volumes of hazardous waste. In this study, we developed a novel and sustainable process to recycle REEs from WEEE, NiMH batteries in particular. The developed process relies on supercritical fluid extraction (SCFE) utilizing CO2 as the solvent, which is abundant, safe, cost effective, and inert. The effect of seven operating parameters, namely temperature, pressure, residence time, sample to chelating agent ratio, agitation rate, complex formulation, and methanol addition on REE extraction efficiency was investigated, and optimum operating conditions were determined. This work is the first to utilize a very efficient and safe process that runs at low temperature to extract metals from postconsumer products with minimum hazardous waste generation, while offering about 90% leaching efficiency for REEs. We expect our process to find widespread applicability in urban mining of REEs using green chemistry.

By Santhanam Ramesh

"The shell (exoskeleton) waste of shellfish such as shrimps and crabs is the raw material in the extraction of chitosan, a polymer. Chitosan has several medicinal values such as reduction in cholesterol, urea and creatine in the blood. It is estimated that about 40000 tonnes of chitosan may be obtained from all chitin yielding invertebrate sources of India and a foreign exchange of 600 million US$ could be earned annually. Awareness has to be created among sea food processors to put up plants to convert shellfish wastes into chitosan. Similarly pharmaceutical industries may use chitosan in the development of new drugs. Types of training and awareness programmes to be organized for entrepreneurs, sea food processors and pharamacists are discussed in this paper.IntroductionIndia earns annually foreign exchange to the tune of 0.8 million US$ by exporting processed marine crustacean shellfish resources such as shrimps, crabs and lobsters (Figure 1) through 300 sea food processing industries. At present, only a small quantity of shell wastes (exoskeleton) generated from the above is utilized as an ingredient in fish feeds and hence much of the wastes are disposed off either as land fill or by direct dumping in sea. These wastes containing primarily chitin could be the major raw material for the production of a proteinaceous byproduct viz. chitosan, a highly valued pharmaceutically important source"

Jan 1, 2008

By Eliezer Martinez-Jimenez, Gretchen T. Lapidus

"Electro-assisted reduction is an effective pretreatment to render chalcopyrite less refractory towards oxidative leaching. In this process, chalcopyrite is selectively converted to chalcocite or copper metal in an electrolytic cell under ambient conditions, while ferrous ion is leached into solution. However, the reaction velocity is hampered by the formation of a ferrous sulfide passivating layer on the solid surface, especially at elevated solid to liquid ratios. In the present work, several strategies for overcoming this problem were evaluated. On one hand, specific ligands for ferrous ion were added in order to increase its solubility and, on the other, an anode material which promotes the oxidation of the sulfide ion was chosen. Leaching tests showed citric acid to be an effective ligand for both ferrous and ferric ions and, in combination with a lead-silver anode, significantly increased the kinetics of chalcopyrite reduction and subsequent copper leaching.IntroductionAttempts to oxidize chalcopyrite at a rapid rate in aqueous solutions, below their normal boiling point, have met with difficulties because of passivation by some of its own components. An alternative line of research explores reductive pretreatment, transforming the chalcopyrite into less refractory copper phases, which can later be oxidized. A recompilation of these efforts up until 2000 was published by Dreisinger and Abed [1]. However, this practice usually requires large excesses of reducing agents, such as copper, lead, aluminum or iron, and in this last case at near-boiling temperatures, in highly"

Jan 1, 2012

By Jeong-Soo Sohn

Physical treatment and chemical treatment of spent lithium-ion battery were studied in our research team. Especially we developed two types of acidic leaching for crushed powders containing LiCoO2 of spent lithium ion battery. One of them is sulfuric acid leaching with H2O2 as a reducing agent. The leaching rates of cobalt, lithium and the other metals were above 99 % at the condition of 2 M H2SO4, 10 vol. % H2O2, 75 °C, 300 rpm agitation speed, 250 g/5L solid liquid ratio and 75 minutes reaction time. And the other leaching process is the oxalic acid leaching. In this process more than 99% of Li and less than 1% of Co were dissolved at the condition of 3M oxalic acid, 80°C reaction temperature, 300rpm agitation speed, 50g/L initial solid/liquid ratio and 90min extraction time. Each process has its advantage and disadvantage. In sulfuric acid leaching, leaching reagent is very cheap and cobalt could be recovered into cobalt hydroxide. On the other hand, oxalic acid is more expensive than sulfuric acid but lithium could be dissolved selectively. Also cobalt could be recovered into cobalt oxalate and it could be changed into cobalt oxide after heat treatment. In order to select the effective recycling process, recovery rate and purity of cobalt hydroxide and cobalt oxalate were compared and it was investigated which process was more environment-friendly and economical.

Jan 1, 2006

By Guanghua Wen, Jian Li, Mingmei Zhu, Fei Xiong, Shengjian Cao

"Small inclusions removal from molten steel in a continuous casting tundish by gas bubbles, which were generated in the turbulent flow region by introducing inert gas, was analyzed theoretically and the inclusion-bubble adhesion and flotation process was also observed by high-speed photo-graph in water model. Results showed that small inclusions in the range of 20-50µm removal from molten steel by bubbles flotation involves three stages: contact, adhesion and flotation. The inclusion-bubble adhesion processes include two ways: inclusions adhering to the upper part of the bubble and inclusions adhering to the lower part of the bubble. As the bubble floats up, the number of inclusions adhering to the bubble are increased. The proper size of bubbles, which could enhance small inclusions removal efficiency, should be controlled in the range of 1-2mm.IntroductionReducing inclusions content in molten steel is a very important way to improve quality of steel, and one of the main tasks in steel making process.A variety of methods have been used for inclusions removal in molten steel. At present, the main approaches to remove inclusions are gas stirring, slag cleaning, filtering, centrifugal separating, and by means of ultrasonic or electromagnetic field. Among these techniques, gas stirring is the most widely and effectively method for inclusions removal. Inclusions in molten steel will be aggregated and generated to form larger size inclusions, and subsequently floated to the surface of molten steel by buoyancy; meanwhile, some inclusions will be adhered to bubbles and floated together to metal-slag interface where inclusions are absorbed by the covering slag layer. Some research work showed that flow behaviors of small bubbles are different from that of big ones [1-2], and smaller bubbles are more efficiency for fine inclusions removal in molten steel.There are many methods to generate bubbles. During steelmaking process, highly turbulent flow in the ladle shroud can split introduced inert gas into small bubbles, which enhances the removal of fine inclusions from molten steel. Turbulent flow of molten steel injected into tundish from ladle shroud has a high speed and it is a strong turbulent area in continuous casting. The gas can be introduced into the shroud below the slide gate. The high turbulence flow would break up the gas into small gas bubbles. Fine inclusions will be easily adhered to small bubbles and subsequently floated to the surface of molten steel. Generation of small bubbles in ladle shroud have been studied in some literatures [3-4]. Some research have analyzed the fine inclusions removal with injecting gas from the ladle shroud by mathematical simulation, and the results show that the refining method can obviously improve the removal efficiency of fine inclusions in tundish [5-8]."

Jan 1, 2013

By Jing Zhang, Chenguang Bai, Fusheng Pan

"The microstructure and hot deformation behaviour of an Er-modified Mg-Zn-Ai alloy were evaluated. The results showed that the addition of rare-earth Er changed the morphology of the quasi-continuous grain boundary networked eutectic compound to globular particles. Moreover, a self-strengthening effect was identified for the alloy, which determined its deformation behavior. After hot extrusion, the yield strength and elongation to failure of the Mg-Zn-AI-Re alloy at 200°C were increased by 105% and 120%, respectively, due to an emerged dynamic precipitation strengthening mechanism.IntroductionMagnesium alloys are attracting increasing attention for applications in automobile, electronic devices and hand tools for weight reduction and higher fuel efficiency, because of their lightweight and a high specific strength. However, application of Mg is still very limited. The largest applications are still those non load-bearing castings used at room temperature, such as box case, housing, and covering. One of the main reasons is the inadequate absolute strength both at room temperature and elevated temperatures (> 100°C) of the commercially used AZ, AM series alloys, due to the incoherent interface between the secondary phase y-Mg17AI12 and Mg matrix, as well as the low thermal-stability of the y phase [1]. Besides, the heat-resistant magnesium alloys which contain rare earth (Re) as the main alloying element are very expensive. The other reason is their poor deformability. The key solution is therefore to develop low-cost heat -resistant wrought alloys."

Jan 1, 2012

By K. Verbeken, E. Wettinck, M. Verhaege

Iron (III) can easily and selectively be removed from acidic sulphate solutions with organo-phosphoric acids like Di-2-Ethyl-Hexyl-Phosphoric Acid [D2EHPA]. Stripping of the iron (III) loaded organic, however, is difficult unless highly concentrated inorganic acid solutions are used. In this paper results are shown for the enhanced stripping of iron from loaded D2EHPA by electro-reduction. The loaded solvent is contacted with a 2 M H2SO4 solution, which is continuously recycled in an electrochemical reactor where iron (III) is reduced to iron(II). As iron (II) is not extracted by D2EHPA, the equilibrium for iron (III)- D2EHPA is shifted towards the aqueous iron (Il)-sulphuric acid solution. The electro-reduction unit is a vessel with separated catholyte and anolyte chambers. The catholyte is the actual stripping solution where iron (III) is reduced to iron (II) on a stainless steel electrode. The anolyte is a 2 M H2SO4 solution where oxygen is evolved on a lead alloy electrode. A sintered glass plug separates the compartments. With this unit, enhanced stripping of iron from the solvent is possible under mild acid conditions [2 M H2SO4], and a concentrated ferrous sulphate solution can be obtained. The results shown have mainly been obtained by studying the parameters affecting the electro-reductive stripping of a D2EHPA loaded organic phase in a batch reactor. From an iron (IH)-saturated 20 vol. % D2EHPA solvent containing ~ 12.5 g/1 Fe (III) over 90% of the iron can be stripped in one stage with a 2 M H2SO4 solution at 50°C. It is shown that in this way it should be possible to obtain a concentrated ferrous sulphate solution which can be processed downstream to recover a pure iron product.

Jan 1, 2000

By Md Sazzadur Rahman

Electrochemical Impedance Spectroscopy studies were conducted on two organic thermal energy storage materials; Neopentylglycol (NPG) and 2-Amino-2-Methyl-1,3-Propanediol (AMPL). The ionic conductivities and dielectric relaxation times in the low temperature ordered a-phase (monoclinic for both NPG and AMPL) as well as high temperature orientationally disordered cubic y-phase are reported.

Jan 1, 2006