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By Toshiaki Tsuru, Takeshi Ohgai, Hisaaki Fukushima, Shigeo Kobayashi, Tetsuya Akiyama

"Electrodeposition behavior of Zn-Cr alloys from the methanol baths was investigated. In the methanol baths of low Cr3+ concentration, Cr (III) compound was incorporated in the deposits and no lusfrous Zn-Cr alloys was deposited. However, Cr was existed as metallic state in the deposits obtained from the baths of higher Cr3+ concentration. With an increase in water content in the baths, the chemical state of Cr in the deposits changed from metallic to trivalent state. Under the condition that metallic Cr can be electrodeposited, Zn deposition was significantly polarized to the potential of Cr deposition.INTRODUCTIONAn attention has been paid to Zn-Cr alloy plated steel sheet because of its excellent properties for body panels of automobile and electrical appliances [1]-[4]. This plating process can be operated using the sulfate solutions containing Cr3+ ion [1] - [6].In decorative single Cr plating, on the other hand, many attempts have been made to electroplate Cr from trivalent electrolytes, which is motived by environmental deficiencies of the presently used hexavalent process [7]. [8]. However, it has been reported that in the aqueous solutions the behavior of the electroreduction of 0 3+ is atypical due to the complicated nature of the chemistry and electrochemistry of cr3+ species [9]-[11]. Even in Zn-Cr alloy plating, it is difficult to codeposit metallic Cr with Zn in simple sulfate electrolytes [l]-[4], [12]. Therefore, it can be expected that the electrodeposition behaviors of Zn-Cr alloys as well as Cr are significantly changed when the electrodeposition is conducted in non-aqueous plating solutions.In this study, the electrodeposition of Zn-Cr alloy was conducted from methanol solutions to clarify the electroreduction mechanism of Cr3·-Cr0 in the alloy deposition process."

Jan 1, 2000

By D. J. Adams

Cyanide heap leaching is the predominant technology used in processing low-grade gold ores. During closure ora heap leach operation, residual cyanide must be removed from the process and waste solutions, as well as the heap. Biological cyanide oxidation is a proven, economical technology for destroying cyanide in process and waste waters and spent heaps; The use of biological cyanide degradation eliminates the need for toxic or corrosive chemical oxidizers and has- been implemented at full scale at treatment costs usually <$0.50/1,000 gal. The Applied Biosciences biological cyanide destruction (BCND?) process has been demonstrated to effectively treat cyanide, concentrations up to 350 mg/L. Treated process solutions and wastewaters also contained other contaminants such as arsenic, copper, iron, silver. selenium, mercury, nitrate and zinc, much of which was removed in the cyanide degradation process. Under optimal conditions, microorganisms can rapidly oxidize free cyanide in some process solutions from over 250 mg/L down to 0.1 mg/L in 4 to 5 hr. Cyanide is degraded to ammonia and carbon dioxide, with 50%ofthe cyanide carbon liberated as C02. In general, carbon tank based bioreactors degrade cyanide at significantly higher rates than process or wastewater pond configured treatments, which usually degrade cyanide-more rapidly than in heap treatments. Investigation of cell-free enzyme preparations as an alternative to live microbial cyanide degradation shows promise. Advantages of enzymes over live microbes for cyanide degradation include: (I) the ability to tolerate and degrade higher cyanide concentrations (> I ;000 mg/L), (2) nutrients to support live microbial cells are not required, (3) the effects of other toxic contaminants, such as metals, found in mining waters-are eliminated and (4) the potential for greatly increased kinetics.

Jan 1, 1998

By Bernd-Arno Behrens, Klaus-Georg Kosch

"In times of increasing energy costs automotive lightweight construction is gaining in importance. This paper deals with the production of hybrid steel-aluminum compounds by forging. The compound forging process is a promising method to successfully manufacture functional parts by applying resource-saving process steps. Nevertheless, challenges resulting from different material properties must be solved.The heating of hybrid material work pieces made of steel and aluminum is a great challenge. Steel is forged at a temperature of at least TSt =900 °C, while aluminum should not exceed a temperature of TA1= 500 °C. For achieving the required temperature gradient extensive experimental investigations have been carried out. Intermetallic phases form during the manufacturing process and can influence the bonding and the global part quality. In addition, methods for the characterization of the joining zone between the materials steel and aluminum are analyzed and the factors influencing the formation of intermetallic phases are determined experimentally.IntroductionIn times of increasing energy costs and stricter conditions relating to environmental protection, automotive lightweight construction is gaining in importance. The production of hybrid compounds by forging is a promising method to manufacture functional parts by applying resource-saving process steps. In compound forging a hybrid raw part consisting of a solid core, which is enclosed by a hollow casing, is joint in the forming process. This results in a graded material structure in the part in which the mechanical properties can be specifically adapted to the requirements. Compound forging is the form joining and/or firmly bonded joining of at least two different materials while plastic shape forming occurs (Figure 1)."

Jan 1, 2012

By R. M. G. S. Berezowsky

Treatment of Hudson Bay Mining and Smelting Co. Ltd. (HBM&S) zinc concentrate in the Sherritt zinc pressure leach process produces a residue containing elemental sulphur, residual sulphides, precipitated iron species, si1ver and gold. Flotation of the residue recovers most of the elemental sulphur and residual sulphides to the concentrate, leaving iron oxides and bask sulphates in the tailings. The tailings also contain most of the sflver and some gold. Direct cyantde leaching of the oxide tailings (220 g/t Ag, 1.4 g/t Au) was capable of leaching most of the gold, but only a minor portion of the silver. This paper reports testwork, conducted by Sherritt on behalf of HBM&S, to define a process for a high recovery of the precious metals from the oxide tailings. A si1ver enhancement treatment, consisting basically of digestion of the residue with lime at 90°C to render the silver amenable to enhanced recovery by subsequent cyanidation, was selected as the most promising approach. Batch silver enhancement and cyanidation tests showed that treatment of the oxide residue with 80 kg/t CaO at 90°C for 1 to 2 h increased the silver extractability in subsequent cyanidation from <20% to 96%. A 96 h continuous miniplant test (1 kg/h solids feed rate), of a circuit including a silver enhancement treatment step followed by conventional cyanidation and carbon in pulp silver and gold recovery, confirmed metal recoveries to the carbon of 90% Au and 96% Ag. Reagent consumption rates were 1ess than 100 ?kg/t CaO and 5 kg/t NaCN.

Jan 1, 1990

By Kim Verbeken, Evelien Van de Steene, Marc Verhaege, Jeriffa De Clercq

"AbstractThe industry is confronted with stricter discharge levels and an increasing awareness to avoid toxic waste (such as heavy metal containing sludge obtained in physicochemical water treatment) and recover valuable metals. This can be realized by ion exchange or by electrodeposition. Both techniques however show an optimum concentration range to efficiently remove and/or recover metals: electrolysis can recover the metal in its metallic form but suffers from low efficiency when applied to diluted solutions, whereas ion exchange can only be applied economically in the low ppm range.A combination of ion exchange followed by electrodeposition was applied to an industrial wastewater. The strong acidic ion exchange resin was stripped with H2SO4 giving a solution of 9g/L nickel. From this solution, nickel was electrodeposited in an ammonia buffer on a Ti-mesh cathode with high current efficiency. It is shown that organic compounds (surfactants, brighteners, …) present in the industrial wastewater do not influence the recovery process.IntroductionAlmost all rinse waters emerging from metal plating plants are generated during the washing operation of plated materials. These solutions with low metal content must either be recycled within the process or be discarded to the surface water after decreasing their metal content to acceptable levels determined by the local environmental regulations, which become more and more stringent. Today, the most commonly used practice is a physico-chemical treatment (precipitation) and a resin post treatment to meet the standards. A more sustainable approach should use a technology to recover efficiently the metal or metal salt without the production of sludge and the effluent should be consistent with environmental regulations."

Jan 1, 2008

By William Petruk

The behaviour of sphalerite during mineral beneficiation of base metal ores has been studied at CANMET and other institutes for at least 15 years by determining the liberations of sphalerite in mill products and calculating the recoveries of liberated and unliberated sphalerite in zinc concentrates. Sphalerite in base metal ores commonly occurs as layers and as interstitial material between pyrite. Layered sphalerite is generally liberated during primary grinding, but interstitial sphalerite requires re-grinding to achieve liberation. Around 95% of liberated sphalerite is generally recovered in zinc concentrates frau zinc circuit feeds. A series of tests was conducted on sphalerite in the ore of Brunswick Mining and smelting during a continuous fine tuning operation of the concentrator. It was found that a grind of 80% minus 37 micrometres was required to liberate the interstitial sphalerite. The fine grind increased Zn recoveries from 75% to 78-80%, but produced liberated slimed sphalerite which was lost. Since regrinding to a fine grain size is needed to obtain the desired sphalerite liberation, a method of recovering the slimed sphalerite is required.

Jan 1, 1990

By Laszlo Kadar, J. D. Lavers

"In the continuous casting of aluminum killed steel, the tundish nozzle often experiences clogging problems. Water model studies have shown that the clogging problem is dependent on the flow pattern in the nozzle entry region. In particular, the flow can separate at the entrance to the nozzle, leading to the development of a recirculation region. Although a nozzle can be designed such that no recirculation develops, even a small misalignment from the vertical positioning of the nozzle may render the design ineffective.To reduce the possibility of nozzle clogging, the recirculation zone must be reduced or eliminated. This may be achieved by moving the fluid downwards or raising the turbulence level in the separation region. In the case of a tundish nozzle, it is proposed that this can be achieved by using electromagnetic forces.To generate the required electromagnetic force, two systems are considered. The first is based on injecting a DC current; the second by using electromagnetic induction. Both methods are described in this paper. Order of magnitude calculations are provided to illustrate that both methods are essentially feasible. The performance of each method in terms of modifying the turbulent flow characteristics in the nozzle entry region is then examined using a numerical model. It is shown that both methods can greatly reduce the recirculation zone. A cylindrical nozzle was chosen for the model studies since it represents a worst case situation.On the basis of the model studies, it can be concluded that whereas both of the proposed methods have the potential to reduce the troublesome recirculation zone, the induction method appears to be simpler in terms of practical implementation."

Jan 1, 1999

By Xiangru Chen, Honggang Zhong, Qijie Zhai, Qingqing Sun

"A horizontal directional solidification equipment, with an in-situ pouring system, was employed to physically simulate the solidification behavior of continuous casting. In this paper, the 2304 duplex stainless steel (DSS 2304) was investigated using this equipment due to its microstructure produced by continuous casting process was usually not satisfied. The grain size combined with the position of columnar to equiaxed transition (CET) of DSS 2304 were observed and the results showed these microstructure characteristics were very close to those of the continuous casting slabs. In addition, the influences of pouring temperatures and cooling conditions on the CET behavior were investigated. The results revealed that the length of the columnar grains decreased with decreasing the pouring temperatures and flow rates of the cooling water. Besides, the content of austenite decreases with increasing the distance from the chilled sidewall.IntroductionDuplex Stainless Steels (DSSs) have been widely used in industry for their excellent mechanical strength and superior corrosion resistance in Cl- environments when compared with other stainless steels [1,2]. Their good performances are mostly on account of the duplex phase structure-ferrite (d) and austenite (?) and the high proportion of alloying elements. Although, DSSs have good ductility, but worse formability compared to the austenitics, and this is the key to restrict DSSs application [3]. This is due to the differences properties between the two phases. The hot workability of ferrite (d) is better than austenite (?) and exhibits a lower flow stress during hot rolling processing [4]. The early workers had revealed that coalescent force of phase interface, microstructure, difference of mechanical property between two phases and the precipitations are the main factors affecting the formability of DSSs [5,6]. Another important reason that affects the alloy’s mechanical properties is columnar to equiaxed transition (CET) [7]. It often occurs during continuous casting solidification process and induces inhomogeneous mechanical properties and the microstructure varies with different processing parameters, such as pouring temperatures, cooling conditions (water flow rates in the cooling zones) and casting speed [8]."

Jan 1, 2012

By Dariusz Kopyci ski, Józef Dorula

The study proves that by introducing the iron powder and disintegrated steel scrap to low-sulphur cast iron still before the inoculation carried out with a conventional graphitising inoculant, the mechanical properties similar to those obtained during the inoculation treatment carried out on cast iron with the recommended high sulphur content are achieved. The said operation increases the number of crystallisation nuclei for dendrites of the primary austenite. In this case, the iron particles act as substrates for the nucleation of primary austenite, due to a similar crystallographic behaviour of the regular face centred cubic lattice The more numerous are the dendrites of primary austenite, the less free space is available in the interdendritic spaces for the formation of graphite eutectic grains, which makes the structure more refined (more eutectic grains) and the mechanical properties higher.

Jan 1, 2016

By R. Moreau, V. Uspenski, K. Messadek, Y. Delannoy

Experiments and numerical simulations have been carried out to investigate the properties of quasi-2D turbulence. A new mercury model experiment has been built and tested in a uniform magnetic field up to 6T, (Ha~ 1000), ensuring a better two-dimensional behaviour than earlier versions (Alboussiere et al., 1997), limited to 0.2T. The quality of the experimental results has been improved in order to get wave number spectra (instead of frequency spectra) and higher signal over noise ratio (due to the higher magnetic fields). In parallel, some two-dimensional "direct" numerical simulations were performed using a commercially available code to solve a 2-D motion equation involving a source term to model the Hartmann layer. This term is derived from the condition of closure of the electric current, which allows to transfer the Hartmann effect into the 2D-core flow without simulating the layer itself (Sommeria & Moreau, 1982). No subgrid scale modelling is needed in such a two-dimensional situation where most of the energy is carried by the large scales.

Jan 1, 1999

By Kang-In Rhee

A series of processes to recover the gold from electronic scrap which contains initially about 200-600 ppm Au have been developed. First, mechanical beneficiation including shredding, crushing and screening was employed. Results showed that 99 percent of gold component leaves in the fraction of under 1 mm of crushed scrap and its concentration was enriched to about 800 ppm without incineration. The scrap was leached in 50% aqua regia solution and gold was dissolved completely at 60°C within 2 hours. Other valuable metals such as silver, copper, nickel and iron were also dissolved. This resulting solution was boiled to remove nitrous compounds in the leachate. Finally, a newly designed electrolyzer was tested to recover the gold metal. More than 99% of gold and silver were recovered within an hour in electrowinning process.

Jan 1, 1995

By Qingchun Yu, Bin Yang, Yong Deng, Heng Xiong, Fei Wang, Minxiu Chen

"Metal aluminum produced by non-electrolysis process received much attention due to its lower energy consumption. In this paper, carbothermic reduction and carbothermic-chlorination of alumina in normal pressure and vacuum were studied. The products were examined by means of XRD, EDS and SEM. During the carbothermic reduction process using carbon reductant in normal pressure, no metal aluminum was found. However, when coal was used as reductant, a mixture containing metallic aluminum, A14C3, and silicon was obtained, but metallic aluminum couldn't be separated from the mixture. During the carbothermic-chlorination process in vacuum, Al404C and Al4C3 were produced by the reaction between alumina and carbon, and Al Ch gas reacted with Al404C and Al4C3 to produce Al Cl gas. Metallic aluminum was produced due to the disproportionation of A!Cl gas and condensed on the collecting plate. Meanwhile, the initial temperature of carbothermic reduction of alumina reduced in vacuum compared with that in normal pressure.IntroductionIndustrial production of primary aluminum is carried out in alumina cell by the so-called Hall- Heroult process, necessitating the use of very high currents of low voltage. The alumina from which metallic aluminum is gained must be chemically pure, otherwise impure metal results. The main drawbacks of the electrolytic production are its very high energy consumption, the release ofperfluorocarbons, and the high specific C02 emissions [1]. During the past years, there were a lot of attempts to produce metallic aluminum by carbothermic reduction of A1203 [2, 3]. Cox [4] determined the vapor pressure over the A1203-C system and performed X-ray diffraction analysis of condensed products. It was demonstrated that an increase in the carbon content in the system leaded to the sequence of transitions: A1203~Al404C~A1zoc~A14C3 ~AI [5]. In any carbothermic reduction process for aluminum, extremely high temperatures (2000 °C ) were required [6]. In spite of considerable effort, the carbothermic reduction of alumina to aluminum remains a formidable technical challenge, due to the high temperatures required, and to the formation of aluminum carbide and oxycarbide byproducts [7]."

Jan 1, 2013

By Jinfu Xu, Youqing Cao, Yuting Lv, Hang You, Peng Jiang

"In present work, we reported the fabrication of composites consisted of M42 powder metallurgy high speed steel and 45 steel at one step via spark plasma sintering (SPS) technology. The interface microstructure, compositions and microhardness with the interface forming mechanism were investigated. The results show that the morphology and microhardness within the M42/45 steel interfaces exhibit a gradient distribution. The interfaces possessed a transition layer up to 10.2 ?m with few distortions and microcracks. The formation of M42/45 steel interfaces were driven by both fusion and diffusion processes. The former one was primary at the early sintering process, while the later one becomes dominant over the followed sintering process.IntroductionPowder high-speed steels have been widely used in cutting tools, cold-hot tools and dies, as well as in cut materials and structure parts with wear resistance and high-temperature resistance, due to its high hardness, good wear resistance, desirable cutting toughness and favorable hot hardness [1-2]. For materials of some parts in practical production, not only the favorable toughness is required to resist the impact action, but also the high hardness and exceptional wear resistance are demanded. According to the functional requirements and working conditions, bimetal composite materials are prepared in a certain mode, proportion and distribution, by designing two metals with different chemical and physical properties [3-6]. Considering the composites exhibit different properties in different positions of the parts with a combination of the advantages of two metals, they can obtain enhanced properties that the single one can not achieve."

Jan 1, 2012

By H. Kaffash

Ferromanganese is a ferroalloy with high manganese content which finds many uses for example as deoxidizer in steelmaking industry. However, there is very little data on the dissolution rate of carbonaceous materials in Mn containing metals. In this paper, the kinetic analysis of carburization reactions is investigated for Mn–Fe alloys. Dissolution rate of graphite in pure iron and four different alloys with 10 wt%, 40 wt%, 60 wt% and 85 wt% manganese at 1823 K was studied. Results showed that the dissolution rate of carbon from graphite increased with increasing time for all alloys. The dissolution rate constant increased with the increasing manganese content from 6.5 × 10−3 cm/s for 0%Mn to 23.6 × 10−3 cm/s for 85%Mn.

By D. I. Davidov, D. A. Shishkin, M. B. Rigmant, E. P. Romanov, N. N. Stepanova, N. V. Kazantseva

The Co-19 at.%Al-6 at.%W alloy was prepared by two methods of casting. We used arc melting under an argon atmosphere with casting into a copper water-cooled casting mold and induction melting furnace with casting into a ceramic Al2O3 mold. According to the X-ray and SEM analyses, phase compositions depend on the cooling rate of the ingot after melting. After arc melting, the cast alloy has a three-phase structure, consisting of  cobalt (FCC), intermetallic phases CoAl (B2) type, and Co3W (DO19) type. After the induction melting, the alloy has a three-phase structure, consisting of  cobalt (FCC), intermetallic phases CoAl (B2) type, and Co7W6 () type. All phases in the investigated ternary alloy at the room temperature are ferromagnetic. Curie temperatures of all obtained phases were defined. It is shown that the magnetic properties of the studied alloy are typical for soft magnetic materials.

Jan 1, 2015

By Honggang Zhong, Tan Yi, Qijie Zhai, Zhao Dan, Xinping Mao, Huigai Li

"The influence of superheat degree on the distribution and volume content of inclusions were studied in 65Mn thin slab produced by compact strip production(CSP) in Zhujiang Steel in China, The results showed that the diameters of inclusions are mainly less than 5µm. Most of the inclusions gathered at the 1/4 thickness direction for the thin slab of 27? superheat degree, compared with the center position for that of 37?. There are more inclusions larger than 50µm in the low superheat samples, which is caused by the short floating time. In addition, the inclusions were observed and analyzed by metallurgical microscope, SEM and EDS in order to ensure their composition, type and further find their source. It was find that the types of these inclusions mainly are Al2O3, SiO2,CaO and their composites, a few of them are TiN and MnS.IntroductionIt is well known that inclusions have a great impact on the strength, plasticity, fracture toughness, cutting performance, fatigue property and corrosion resistance of steels. Especially, with the demand for thinner slab, the cleanness is increasingly becoming more significant as a quality criterion[1]. High manganese and carbon steels not only demonstrate high strength but also proper plasticity. There are many problems unsolved for 65Mn steel as a result of the low solidification rate, bad thermal strength, crack sensitivity and low casting temperature[2,3].The superheat of the molten steel has a great impact on the erosion of refractory lining, molten steel fluidity and non-metallic inclusion behavior[4]. The serious erosion situation of ladle lining, nozzle and casting tundish will give rise to more inclusions at a high superheat. Meantime higher superheat will make second dendrite arm spacing coursing and element segregation which lead to inclusion, bubble formation and shrinkage cavity. On the contrary, it is hard for non-metallic inclusions to float up with a low superheat value. Inclusions of 65Mn steel, which produced in different superheat condition by CSP, were studied for the sake of higher slab properties including statistics and EDS analysis."

Jan 1, 2012

By Lei Wang, Jianjun Wang, Lingen Luo, Zhengbang Li

Dearsenication in molten steel was studied by adding Ca-Fe Alloy-based arsenic removal agent. In order to improve the utilization rate of Calcium Iron Alloy and improve arsenic removal ratio, [O] is less than 0.0005% and [S] is less than 0.0035%, Al is added into the molten steel. In the processes of adding CaO-Al2O3 based alkalinity slag for arsenic removing in molten steel (initial arsenic content is 0.0080%), arsenic removal ratio reaches 50% when Ca-Fe Alloy addition amount is 18%. During the arsenic removal experiment, adding Rare Earth promotes the arsenic removal reaction and makes the arsenic removal more effectively.

Jan 1, 2015

By Jae-Ho. Lee

For some electronic applications where a dispersed electrically-conductive particulate-phase is employed, the conductivity of the surface (or near-surface region) of the particles provides for the primary mechanism which determines its electrical conductivity. Particles of a less expensive material, which may have desirable thermal-expansion properties, when coated with silver offer a means of also obtaining desirable electrical properties and at low cost. The research conducted was focused primarily on the development of silver-coated tungsten particles for thick-film polymeric conductors. The ammoniacal electrolyte was formulated from silver-nitrate, glycine inhibitor and formaldehyde reductant. The reduction, and subsequent deposition, of silver occurred selectively on the surface of the tungsten particles. Coated particles were assessed by SEM imaging. The thickness of the silver coating was estimated to be approximately 100nm on the basis of a mass account and the coating being uniform. The electrical conductivity of a silver-coated tungsten-powder pellet was found to be similar to that of a silver-powder pellet, of identical geometry.

Jan 1, 1997

By Takeshita. Takuo

"In this work, the progress of the HDDR process is discussed mainly on the Nd-Fe-B magnet system. There are three technologies being used for the Nd-Fe-B permanent magnet production; the sintering technique, the rapid quenching annealing and the HDDR process. The HDDR process utilizes· the HDDR phenomenon, in which hydrogen absorbing intermetallic compounds go through as they are heated in hydrogen atmosphere, Hydrogenation - Decomposition Desorption - Recombination. In the HDDR process, these four steps in the HDDR phenomenon are processed by choosing suitable reaction conditions regarding to hydrogen gas pressure, temperature, rate ·of desorption and etc., and we can produce permanent magnet powders of good magnetic properties with microstructures consisting with sub-micron size crystalline grains. In the anisotropic magnet powders, the sub-micron size crystals are being mostly aligned in the crystallographic c-axis direction. Possible applications of the HDDR process to other systems are also discussed.Microstructures of the Nd-Fe-B Permanent MagnetsIt is well known that magnet properties of magnetic materials are very sensitive to their microstructures [l]. This is seen in almost all magnet materials from soft magnetic materials and hard magnetic materials to magnetic memory materials. In this regard, the production technology is very important for the control of microstructures of permanent magnets The Nd-Fe-B magnet is the most powerful permanent magnet as a practical permanent magnet, and its coercivity force is much dependant on the microstructure as is the case for other permanent magnets."

Jan 1, 2000

By Xiaobing Yang, Abhishek Lahiri, Animesh Jha

"In the FFC-Cambridge process, the cathodic dissociation of oxide and CO/CO2 production on carbon anode is the basis for metal production in a CaCl2 bath. By using an inert intermetallic anode, the CO2 evolution can be eliminated altogether with acceleration in the electro-reduction kinetics. At present the process suffers from slow reduction kinetics of TiO2 to Ti metal, which can be enhanced significantly by the incorporation of alkali species in the TiO2 pellet at the cathode and in the CaCl2 bath in the presence of an intermetallic inert anode. Nearly full metallization with greater than 99% of Ti metal containing 1500 ppm of oxygen is possible to achieve in less than 16 hours of electro-reduction. Analyses of phase composition and the microstructures morphology in fully metallized pellets revealed the presence of localized solidified Ti layer, indicating that fast reduction process also involved formation of liquid phase as middle stage reaction. In addition, in situ creation of porosity and maintain higher current level during electrolysis process were two key factors to fully reduction of TiO2.IntroductionDuring cathodic dissociation of TiO2 in a CaCl2 bath and anodic evolution of CO2 on a carbon anode, which is the basis for the FFC Cambridge process [1], the rate of metallization slows down due to the formation of CaTiO3 at the reaction interface. Calcium and alkaline earth perovskites are known for their poor electrical conductivity which adversely affects the overall electro-reduction. One of the ways to increase the porosity is via the addition of polyethylene precursors in the pellet or by directly starting from perovskite [2, 3]. The experimental evidences shown in the literature confirm although the speed of reaction increases, but a complete or near complete metallization is not possible by enhancing the in-situ porosity alone, as the insulating perovskite is very slow to decompose under the equilibrium that prevails in the cell. Plethoric evidences on carbon anode show with the current decrease gradually, and finally stabilize at a very low value between 0.2 and 0.4 A, which is a testimony of the presence of perovskite insulating barrier in the current path. Our aim in this paper is to demonstrate the mechanism of enhanced electro-reduction when alkali ions are present in the oxide pellet at cathode and in the bath. We also show for the first time the use of an intermetallic anode for Ti-metal production using the FFC Cambridge process."

Jan 1, 2009