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By JiaPeng Xu, Brian Lo, Uday B. Pal, Yihong Jiang, Soumendra N. Basu

"The Solid-Oxide Oxygen-Ion-Conducting Membrane (SOM) electrolysis process has been successfully tested on a laboratory scale, producing silicon directly from silica in a cost-effective and environmentally friendly way. A yttria-stabilized zirconia (YSZ) tube, closed at one end was employed to separate the molten salt containing dissolved silica from a liquid metal anode placed inside the YSZ tube. When the applied electric potential between the liquid tin cathode in the molten salt and the anode exceeds the dissociation potential of silica, oxygen ions are pumped out of the molten salt through the YSZ membrane and oxidized at the anode while the silicon cations in the flux are reduced to silicon at the liquid tin cathode. The presence of high-purity silicon crystals on the surface of liquid tin cathode was confirmed by scanning electron microscopy (SEM) and energy dispersive x-ray spectroscopy (EDS). Silicon crystals were extracted from tin cathode by chemical etching.IntroductionPhotovoltaics (PV) generate electrical power by using solar cells, and dramatically reduce the emissions of greenhouse gases (GHG). Through 2006 to 2011, it grew the fastest of all renewable technologies with operating capacity increasing an average of 58% annually [l]. However, the cost of manufacturing solar-grade silicon (SoG-Si) for high-efficiency solar energy production represents a major barrier to achieving the industrial goal for solar power of $1/Wp (watt at peak exposure) which would enable widespread grid parity. The current contract price of silicon to PV manufacturers is $50-$60/kg, with the spot market in 2007-2008 showing prices as high as $300/kg [2]. This makes the development of low cost and environmentally friendly manufacturing of high purity silicon very important."

Jan 1, 2013

By Harold R. Kokal

Lisakovsky is a 3-billion ton oolitic iron ore deposit in north-central Kazakhstan operated by Orken LLP, a subsidiary of Ispat Karmet and the LNM Group. The iron oxide minerals are goethite and limonite. The gangue occurs as discrete quartz grains and an unidentified form of colloidal silica-alumina. The concentrate produced contains about 49.5 percent iron (Fe) and 0.6-0.8 percent phosphorus (P) or 10-20 times the acceptable phosphorus level. The phosphorus is intimately associated with the iron oxide and colloidal gangue, no discrete phosphorus minerals are found, and beneficiation is not possible. Therefore, to reduce the phosphorus, a hydrometallurgical process that includes roasting followed by leaching in dilute sulfuric acid has been developed. Phosphorus extraction is 70-90 percent, with only a minor loss of iron. The process has been tested in the laboratory and in a pilot plant at 50-300 kg/h. Construction of a 900,000 t/y demonstration plant is underway.

Jan 1, 2003

By Bhagyadhar Bhoi, Chitta Ranjan Mishra, Hara Prasanna Mishra

"In the Sukinda Valley of Orissa, India, the total quantity of nickel ore reserves comprising of both lateritic and chromite over burden(COB) have been estimated at around 231 million tonnes containing 0.3 to 0.9% Ni. While mining of one tonne of Chromite ore, around 6-7 tonnes of chromite over burden are removed. These overburden materials are disposed as waste materials, which causes lot of environmental hazards and ecological imbalance. India imports a large amount of nickel and ferro-nickel to meet its growing demands in various sectors. For import substitutions, efforts have been made to produced ferro-nickel from the lean deposits of nickel bearing lateritic ores/ chromite over burden materials by reduction roasting followed by magnetic separation and then the nickel rich magnetic fraction is smelted to produce ferro-nickel. It has been possible to produce ferro-nickel of grade varying from 4-25% nickel.IntroductionDuring mining of chromite ore, large quantities of overburden materials are being generated. The materials amount to approximately 10 million tones per year contain around 0.3-0.9% Ni, 0.02-0.06% Co, 20-50% Fe and 4-9% Cr2O3 depending upon the location and the depth of the mine. These materials presently do not find any application for the extraction of nickel due to lack of a suitable technology. The materials are also unsuitable for ferro-nickel making because of their very high iron to nickel ratio. The country is seriously looking for a suitable technology to utilize these resources as its entire domestic requirements of nickel is met though imports. In this connection, a systematic approach has been made at the Institute of Minerals and Materials Technology, Bhubaneswar to develop a process for ferro-nickel making from this indigenous resource."

Jan 1, 2011

By C. A. Nogueira, F. Margarido

"A research work has being carried out annmg at evaluating the possibility of treating simultaneously several electrochemical systems of spent batteries using the same process, in order to overcome the high costs and difficulties of selective collection and sorting. Zn-Mn02 systems, representing more than 75% of portable battery market, shall be treated in dedicated processes. The treatment assessment using a single hydrometallurgical process of the other major systems (NiCd, NiMH and Li-ion), having Ni and Co as main metals, was the aim of the research work here reported. Sulfuric acid leaching was demonstrated to be adequate for dissolving more than 90% of the metals of interest contained in batteries. The subsequent separation of metals by solvent extraction, using organophosphorous extractants like DEHPA and Cyanex 272, allowed the production of pure solutions of rare earths, cadmium/manganese, cobalt, nickel and lithium, enabling their further recovering.IntroductionRecycling is the best approach for end-of-life management of spent batteries mainly by environmental reasons but also motivated by resources conservation and, in some cases, by economic profits. Most relevant electrochemical systems of portable cells are Zn-Mn02 (ZMB, alkaline and saline), nickel-cadmium (NiCd), nickel-metal hydride (NiMH) and lithium-ion (LIB). These batteries are collected, sorted and usually treated separately, applying for pyrometallurgical or hydrometallurgical technologies, the former being the most common.Several processes have been developed and some of them industrially applied, as described in some available review papers [l, 2]. In Europe for ZMB systems the oldest processes are Batrec [3] and Citron [4]. Although having differences in details, both are based on pyrometallurgical recovery of zinc by distillation, in metallic or oxide forms, being manganese retained in the slag together with iron. Hydrometallurgical alternatives are also available, like Zincex [5] and Recupyl [ 6] processes, both using sulfuric acid solutions as leachant. The application of the existing technologies to battery recycling, instead of using dedicated processes, is other alternative already tested, being the Waeltz furnace or the Imperial Smelting some examples."

Jan 1, 2012

Rapidly solidified TiAl-Cr-xNb-Y(x=2,4,6, at.%) alloys have been produced using a single roller melt spinning method. The microstructure of alloy ribbon was refined and component became more homogeneously by rapid solidification technology. There were two phases in alloy ribbons, including -TiAl and 2-Ti3Al phases, yet the amount of 2-Ti3Al phase in matrix obviously increased by rapid solidification than cast alloys. The micro-hardness testing also carried out. Compared to the cast alloys, the alloy ribbons have much higher hardness.

Jan 1, 2009

By P. R. Taylor

Diamond films have been successfully formed in an inductively coupled plasma (ICP) chemical vapor deposition (CVD) system from several gas mixtures: CH,-H,, C2112-112, and C2112-112-02' Our previous thermodynamic study indicated that the substrate temperature could be lowered by the presence of oxygen species at moderate system pressures (0.3-0.5 atm) and that higher volumetric growth rates required a high temperature source and a moderate pressure system in CVD processing. The principal experimental results were consistent with the thermodynamic predictions. The deposited films were characterized by laser Raman spectroscopy, scanning electron microscopy, and X-ray diffraction. The films were well faceted and uniform, with the growth rates over 10 pm/hr on molybdenum substrates. The crystal size ranged between 1 and 2 microns for a two hour experiment. It was possible to decrease the substrate temperature to below 800 °C in this system.

Jan 1, 1995

By Toshiyuki Kozuka

CdTe semi-conducting materials have been expected as solar cell materials because its theoretical energy conversion ratio is very high. The actual efficiency still low, however, many research works have been done in order to improve the efficiency. And crystal orientation is one of possibilities for that. In this work, a new method using intense magnetic field for a control of texture of CdTe crystals will be proposed, where the CdTe film was electro-deposited under an intense magnetic field. CdTe is less affected by magnetic field, because of its cubic structure, but Cd or Te has hexagonal structure, which is sensitive for magnetic field. In this paper, crystal orientation of Cd or Te film, which can be utilized as basic layer for CdTe deposition, will be developed.

Jan 1, 2006

By Pei-xiao Liu, Han-jie Guo, Yan-xiang Li

The thermodynamic analysis on chromium ore pellets in solid reduction chromium process is carried out, and the result is validated by pre-reduction experiment of cold briquetted chromium ore. Polarization Microscope and SEM are employed to observe microstructure and element composition. The thermodynamic and experimental results reveal the reduction mechanisms at different temperatures in the SRC pre-reduction process.

Mar 1, 2017

By T. T. Chen, J. E. Dutrizac

"Grooved cast Pb-Ag anodes are used by some zinc refineries to improve current efficiency. It was found that the manganese oxide scale formed on a grooved Pb-0.75% Ag anode consists mainly of MnO2, which occurs characteristically in rhythmically banded colloform structures and adheres to a layer of ""Pb02+PbS04"" that oxidized from the anode. The relatively homogeneous and nearly fracture-free morphology of the ""Pb02+PbS04"" layer suggests the relatively uniform corrosion of the anode. Deposition of the Mn oxide initially follows the contours of the anode surface, but the grooves eventually become filled with Mn oxide and gypsum. Hydrous Mn oxides and amorphous Mn oxides are believed to be also present in the manganese oxide scale. Tiny particles of PbS04 and SrS04, together with gypsum, other impurities and micro-pores, tend to concentrate in the grooves.IntroductionManganese is a common impurity in hydrometallurgical zinc processing circuits. The manganese originates from sphalerite (Zn,Fe,Mn)S and from the Mn02 added to the leaching circuit to oxidize ferrous ions [1]. Manganese in the sphalerite follows Zn through the roasting, leaching and purification processes, and is present as Mn(II) in the purified ZnS04 solution. The Mn in the added Mn02 is reduced to Mn(II) during the oxidation of the ferrous ions present in the leach solutions. In both cases, MnS04 is generated, and the MnS04 accumulates in the purified solution. In the cellhouse, Zn is plated at the cathodes to produce high quality metal. The Mn(II) is partly oxidized at the anode surface to Mn(IV), and the Mn(IV) precipitates as a scale on the surface of the anode and as a sludge on the bottom of the electrolysis cells. The presence of a thin layer of manganese oxide scale on the surface of the Pb-Ag anode can minimize the corrosion of lead and, accordingly, reduce the contamination of the electrodeposited zinc. However, a heavy manganese scale build-up can cause ""staining"" of the zinc deposits and reduced current efficiencies. Consequently, periodic anode cleaning to remove excess manganese oxide scale is carried out routinely in commercial operations."

Jan 1, 2011

By David Langberg

Recovery of dissolved copper from discard slags is a critical consideration affecting the economics of copper smelting. Slag cleaning is frequently carried out in electric furnaces, however reduction by injection of natural gas in a holding furnace may offer a lower cost alternative in some circumstances. As the residence time of the injected gas is short, the factors controlling the rate of reduction need to be clarified in order to optimise the design of the slag cleaning furnace. A series of medium scale (200 kg) reduction tests to investigate the rate of reduction of copper-containing slags by injection of natural gas-nitrogen mixtures between 1150-1250C was carried out by CSIRO Minerals. The composition of the gas in the top-space of the reactor was found to be significantly more reducing than the slag, indicating that thermodynamic equilibrium was not established between the slag and the gas in the bubble plume. An apparent first order rate law was observed between the rate of oxygen elimination from the bath and the magnetite concentration of the bath. The dissolved copper concentration was closely correlated with the oxygen potential of the slag, suggesting a partial equilibrium between the dissolved components of the slag. The utilisation efficiency of the natural gas decreased as the natural gas flow rate was increased. The results of the tests tend to indicate that the rate is controlled by a mixed reaction kinetics/ mass transport mechanism. The work was supported by Xstrata Copper ? Mt Isa Mines.

Jan 1, 2006

By Laila A. Guirguis

Impurities are removed from crude phosphoric acid (57.75% P2O5) with a mixture of low and high molecular weight alcohols, one of which is hydrophilic and the other is hydrophobic i.e. methanol and hexanol. In a single stage, the phosphate values segregate to the high molecular weight alcohol fraction and the impurities segregate to the low molecular weight alcohol fraction. The optimum ratio for the extraction is found to be 0.5 part methanol, one part impure acid and four parts hexanol where an extraction percent of more than 95% is achieved. Re-extraction of the phosphate value from the solvent is obtained by 6% phosphoric acid and the different factors affecting the re-extraction process have been studied. Finally, the purified acid is concentrated under reduced pressure and passed through activated carbon column, whereas the alcohols are re-circulated. The produced phosphoric acid was found to be in good match with the international specifications of food grade quality acid. A technological flow sheet is elucidated.

Jan 1, 2006

By Dachun Liu, Wenlong Jiang, Baoqiang Xu, Yongnian Dai, Bin Yang

"In the traditional method for refining of indium, glycerin-KI and glycerin-NH4Cl are used as electrolytes to remove Cd and Tl by electrolytic refining, which produces In with a purity of 99.995%. Large quantities of polluted industrial waste water are the result. It is calculated that the saturated vapor pressure of Cd and Tl are between 1-200 Pa, which is much larger than the vapor pressure of In. Thus, the study of removing Cd and Tl was carried out over the temperature range between 700-950 °C and pressures between 1-15 Pa. After vacuum distillation the contents of Cd and Tl in crude indium could sharply fall below 1 ppm..IntroductionIndium is a is a pale blue and silver white metal, and has high ductility [1-2]. Pure indium is generally used as a raw material to produce semiconductor compounds, fluorescent material and ITO targets [3]. Sublimation, zone melting and electrolytic refining are major methods to produce pure indium from crude indium. Electrolytic refining is the main method to product pure indium at present. High productive efficiency, simplicity of operation and short cycle of production are major advantages. However, glycerin-KI and glycerin-NH4Cl are used to remove Cd and Tl in electrolysis method. Large quantities of polluted industrial waste water are the result[4]."

Jan 1, 2012

By Wentao Guo, Xuefeng She, Qingguo Xue, Jingsong Wang

By the coke gasified reaction device and online measurement high-temperature compressive strength apparatus, the variation of pore structures of coke after gasified reaction with CO2 and H2O was investigated. Research illuminating the influences of solution loss rate, temperature, and carbon species on compressive strength of coke was also carried out. The results showed that the total compressive strength was higher than for the reaction with CO2. The high-temperature compressive strength of coke decreased with the increasing of solution loss ratio or temperature after reacting with CO2 and H2O. At the same solution loss ratio, the damage of pore structure to coke strength after gasified reaction with H2O was relatively smaller and the deformation resistance was stronger when compared with that in CO2.

Jan 1, 2016

By Christina V. White

An experimental study was undertaken to investigate the feasibility of utilizing vapor transport for the treatment of heavy metal contaminated smelter soils. The focus of this project was to develop process chemistries that would make incineration a viable process for the treatment these soils. The experimentation concentrated on the elimination of arsenic, cadmium, and lead, and was performed in a laboramry scale rotary kiln setup. Three soil samples from non¬ferrous smelter sites, which contained various concentrations of contaminants, were utilized in the experimentation. Three chemistries were investigated for the volatilization of the heavy metals: Chloridizing volatilization, ferric chloride vapor complex formation, and the use of oxygen potential control. The samples were analyzed for residual heavy metals so that the extractions could be determined. However, the ultimate test was the leachability of the residual arsenic, cadmium, and lead, as determined by the TCLP test. The results firmly establish that incineration is a feasible process for the treatment of metal contaminated soils. It was found that no one process chemistry is suitable for all different soil samples. A two-step process consisting of a reducing step followed by a hydro-chlorination step was required to make Soil Sample-B pass the TCLP tests for all three heavy metals. Soil Sample-A passed the TCLP tests for arsenic, cadmium, and lead using a hydro-chlorination process at a minimum temperature of 700°C. In addition to passing the TCLP mm for Soil Sample-A and Soil Sample-B, 70 to 80 percent removal of the impurities was accomplished. This demonstrates that the leachability of the impurities was decreased primarily due to the removal of a large fraction of the contaminants, Soil Sample-C possessed very high levels of cadmium and lead and only moderate extractions of the impurities were generated from this soil. The arsenic TCLP test was passed at 500'C using a process gas containing ferric chloride and at temperatures of 700°C and above using chlorination of hydro-chlorination.

Jan 1, 1996

By Y. W. Miao

Along the south-west coast of Taiwan is about 550,000 metric tons of heavy sand deposit containing about 10 % black monazite. The Institute has developed a separation process to recover the individual rare earths and the developed process has been commercialized by a local private company. The decomposition of the local black monazite by sodium hydroxide through hydrothermal and fusion methods has been investigated. In the hydrothermal process 4.5 wt. % of aqueous alkali solution was used in an autoclave. In the fusion process, caustic soda (9.8% NaOH) was employed in am open cylindrical reactor. The same product of hydrous rare earth oxides were obtained and then dissolved by hydrochloric acid and the p-H adjusted in order to separate the thorium from the rare earths. After filtration, the filtrate contained rare earth chloride and the cake contained mainly the silica and thorium hydroxide. Both methods give a yield of 90 % with respect to the rare earths recovery. A detailed description of operation and comparison of the two methods are given.

Jan 1, 1989

By Tzu-Chien Lin, Jack Tsai, Ming-Yu Lin, Der-Ray Huang, Jiin-Sen Chen, Jing-Xuan Lin

"In this paper, some DVD-R discs have been selected for long time light exposure test and high temperature and humidity test. Generally, recordable media under long time light exposure maybe be defected seriously. If we use Jitter value 8% as a reference to determine the life time of DVD-R samples, some discs defect after 5 hours of light exposure while some discs can endure over 25 hours. Also if we use reflectivity 45% to determine the life time, some discs defect after 30 hours light exposure while some discs can endure over 40 hours. From our results, the good samples show good characteristics of PI error. The absorption spectrum of recordable media is a good reference to justify the quality of dye media. These results can be used to estimate the life time of recordable discs.IntroductionIn general, the life time of DVD-R with a layer of organic dye recording layer is required for preservation in decades. In addition to optical characteristics and thermal properties, we still need to consider the stability of the dye in recording media. The presentation of the color on organic dye is not only related to the material's property but also related to the light exposure. In this study, we focus on the absorption characteristics and reflectivity of organic dye in optical recording layer after light exposure. The optical properties of discs depend on the functional groups and molecular structure [1]. According to ""DVD Specifications for Recordable Disc (DVD- R)"", the reflectivity should higher than 40%. From measured reflectivity, we can confirm that the important issue is whether dye be affected by light exposure or not. Because each specific functional group absorbs the specific spectrum, we can check the characteristics of functional groups from their UV/Visible Spectra. We also use High-performance liquid chromatography (HPLC) to detect the different components of dye on the recording layer [2]. The jitter value test is to test the error cause by digital signal of recording media. If we use jitter value 8% as a reference to determine the life time of DVD-R samples, the purpose of this study is to investigate the jitter values of recording media after high light exposure and high temperature/humidity test. The results of these test will be helpful for the development of long-life optical storage media."

Jan 1, 2012

By Guohua Bai, Mingjun Rao, Jianchen Lim, Guanghui Li, Tao Jiang

"By using thermogravimetry, optical microscope and chemical phase analysis, the solid-state reduction of carbon-burdened chromite pellets in the absence and presence of additives were investigated. The effects of reduction temperature, reduction time and additives on the metallization of chromite pellet were studied. The results indicate that the pre-reduction ratio of carbon-burdened chromite pellets is improved with the increase of reduction temperature and the addition of additives. The metallization of chromium is increased from 63.9% to 92.8% at 1300 °C for 4h with the addition of 2 wt.% of sodium borate. Investigation suggests that the reduction of carbon-burdened chromite pellets is diffusion controlled. The apparent activation energy without additive is 192.1 kJ/mol, while it decreases to 170.4 kJ/mol in the present sodium borate.IntroductionFerrochrome is used to produce high strength, corrosion resistant, wear-resisting, high temperature resistant and oxidation resistant special steels, and it is becoming one of the most important alloy materials for the production of stainless and high alloying ferritic steels [1-5]. Demand for ferrochrome is steadily on the rise due to the growth of stainless steel industry. Nowadays, more than 80% of the world's ferrochrome is utilized in the production of stainless steel [6-7].Ferrochrome is mainly produced in submerged-arc furnaces (SAF) with chromite lump ore. However, lump ore merely accounts for 20% of the chromite ore output, while fine ore (< 8 mm) accounts for about 80% [8]. Therefore, agglomeration of chromite fine ore is necessary before charging into SAF."

Jan 1, 2011

By Jingwei Lou, Bing Li, Suzhen Li, Miao Shen, Jianguo Yu

"As a main impurity in primary lithium metal, magnesium is difficult to remove because of the very close relative volatility of the two metals. Electrochemical refining provides a possibility to completely remove Mg in the LiCl-KCl melt prior to Li reduction. MgCl2 reduction processes in LiCl-KCl- MgCl2 melt were investigated by cyclic voltammetry (CV), square wave voltammetry (SWV), chronoamperometry and chronopotentiometry. Then potentiostatic electrolysis was carried out and Mg (II) ion was reduced onto a liquid lead cathode from the LiCl-KCl-MgCl2 melt at the Mg deposition potential. The results show that Mg ( II ) is reduced in one step with two-electron transfer. The reduction potential of Mg ( II ) was well defined. The reduction of Mg( II) results in Li ( I ) underpotential deposition at 0.2V more negative potential than that of Mg( II) reduction. Therefore, in order to prevent Li ( I ) from codeposition with Mg, accurately controlling Mg ( II) reduction potential during the potentiostatic electrolysis was necessary. Ninety three to 99 % removal rate of MgCl2 was achieved after 8-12 h electrolysis when liquid lead was used as cathode.IntroductionMetallic Li has been widely used in batteries, light weight alloys and in fusion reactors because of its excellent properties. Currently, the only way in industry to produce metallic Li is by electrowinning from molten LiCl-KCl at about 450 °C [l-5]. LiCl-KCl is the only electrolyte used, because they presents a lower eutectic temperature and KCl shows a slightly higher theoretical decomposition voltage than LiCl, as shown in Table l .The produced metallic Li generally contains 1-2 wt% impurities including Na, K, Al, Ca, Mg, Si, etc. [6l, which are derived from the corresponding metal chloride compounds or metal oxide compounds existing in the LiCl and/or KCl raw materials. These impurities have to be removed by subsequent vacuum distillation at high temperatures to meet the requirements for metal Li purity in the final products. Separation of Mg from Li by vacuum distillation is difficult because their relative volatilities are very close, as shown in Table 2."

Jan 1, 2011

By Shun Myung Shin, Dong Hyo Yang

Cobalt is recovered from square type of spent lithium ion batteries (LIBs) containing 5~20 % Co, 5~7 % Li, 5~10 % Ni, 15% organic chemicals, and 7% plastics together with Cu, Al, Fe, and Mn. The waste LIB was prepared by physical treatment. After screening, the crushed LIBs were separated to +8 mesh, -8/+16 mesh, and -16 mesh powder. Among these, -16 mesh powder was selected for leaching. The leaching test was investigated at 2 M H2SO4, 6 vol.% H2O2, reaction temperature 60 ?, agitation speed 300 rpm, solid/liquid ratio 50 g/ 500 ml, reaction time 1 h. The leaching efficiency of cobalt was more than 99 % and its concentration was 24.9 g/L. For removing of impurities such as copper, iron, and aluminum in the leaching solution before cobalt solvent extraction, the impurities were eliminated by pH control with alkali solution. For selective extraction of cobalt, the aqueous phase removed impurities was equilibrated with different volumes of 0.4 M Cyanex 272 saponified of 50 %. Extraction efficiency of cobalt was about 80 % at first step. Separation coefficient (ßCo/Li) of cobalt and lithium extractions was 206.5. Over 9.0 % of pure cobalt sulfate solution was obtained after stripping with H2SO4 solution.

Jan 1, 2008

By Hiroyuki Sano

Elimination of heavy metals from the incineration fly ash by the chlorination volatilization method had been already developed and the effectiveness of this method was confirmed by the present authors. In this study, this method was applied to the elimination of heavy metals, mainly lead, from the incineration bottom ash. Since the fly ash contains a large amount of chloride, heavy metals in the fly ash are easily chlorinated. On the other hand, the addition of the chlorination agent is a key point for applying this method to the bottom ash, because it hardly contains chloride. The effects of various variables such as a kind of chlorination agent, adding quantity of it and temperature on the elimination ratio were investigated and the harmlessness of the residual ash was evaluated. The preferable condition was proposed from the recyclability of the bottom ash.

Jan 1, 2006