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By Alexandre Chagnes

The extraction properties of two synthesized cationic exchangers, i.e. bis (1,3-dibutoxypropan-2-yl) phosphoric acid (BiDiBoPP) and bis(1,3-diisobutoxypropan- 2-yl) phosphoric acid (IPA), have been studied for the liquid-liquid extraction of Co(II), Ni(II) and Mn(II) contained in 1 M HCl. A comparison of the extraction properties of these extractants diluted in kerosene with Cyanex® 272 shows BiDiBoPP and IPA extract advantageously at lower pH than Cyanex® 272 and a better Co(II)-Mn(II) separation is achieved using BiDiBoPP or IPA than with Cyanex® 272.

By R. M. Taylor

Lime addition to acid mine drainage (AMD) leads to precipitation, predominantly of metal hydroxides and calcium sulfate, and is the benchmark for remediation by precipitation. Geo2 Limited of Melbourne, Australia has developed and patented a novel alternative precipitation scheme based on the formation of mixed valency, M(I1)-M(III), hydroxide sulfate salts. When the composition of AMD is appropriate, the Green Precipitate Process provides a useful and more effective alternative to conventional liming. The characteristics and utility of the Green Precipitate Process are described in terms of the underlying chemistry, and a case study where the Green Precipitate process outperforms conventional liming. A mobile pilot pipe reactor rig which was built by Geo2 to demonstrate the process, and used successfully in both Australia and the United States, is described.

Jan 1, 1998

By M. Nilmani, J. Sofra

The transverse distributions of the solids discharge velocity and mass flux at the discharge end of vertical and inclined lances were measured in order to detennine the transverse distributions of the axial momentum flux, which is a dominant factor influencing the penetration behaviour of particles into melts during submerged injection. The effects of gas velocity (10 - 30 m/s), solids loading (5 - 10), lance length (0.15 - 1.0 m), lance inclination (vertical downward - horizontal) and particle density (2500 - 8900 kg/m3 ) were investigated, while the lance diameter and particle size were fixed at 10 mm and 220 µm respectively. The particle velocities and mass fluxes were measured by image analysis of particles illuminated in a laser-generated light sheet aligned vertically through the axis of the lance at the discharge point. The particle discharge velocity profiles for vertical downward flows were synunetrical about the centre-line of the lance, with the maximum velocities occurring at the centre-line. The velocities increased with increasing gas velocity, increasing lance length and decreasing particle density in accordance with previous observations. The transverse mass flux profiles were also synunetrical for vertical downward flows, however at the lower gas velocities the peaks in the profiles were displaced from the centre-line of the lance by a fractional diameter of about 0.15. The particle discharge velocity profiles become increasingly asynunetric as the lance orientation was changed from vertical to horizontal, with higher particle velocities present near the top wall of the lance. The mass flux profile also became asyrrunetric as the horizontal orientation was approached, however in this case, the profile became biased towards the bottom of the lance. The effect was much more pronounced for a gas velocity of 10 m/s than for 30 m/s, showing the relatively stronger gravitational influence as the velocity was reduced.

Jan 1, 1996

By L. A. Bertram, F. J. Zanner

"The goal of this paper is to present a tool to simulate transient melting of the electrode tip. This capability is needed to develop and test furnace control algorithms since experimental determination is difficult and expensive. Simulation incorporates parameters (including arc voltage, arc current, electrode gap and furnace pressure) from previous quasi steady experiments with 460 mm diameter Inconel 718 electrodes.Cathode heating rates (determined by classical as well as experimental arc models) are linked to these independent variables. After radiative loss adjustments to the heating, transient one dimensional melting is computed. IntroductionThe vacuum arc remelting (VAR) process attempts to improve the physical and chemical homogeneity of a static-cast electrode by remelting and solidification in a quasisteady manner. To achieve steadiness of furnace operation requires automatic controls based on inputs measuring physically relevant state variables of the process. Previous industrial scale VAR studies (1,2,3) involving stainless steels, superalloys, and other alloys have provided a basis on which control strategies of some generality can be proposed (4). Of these measurements, the data for Inconel 718 is the most complete, so discussion in this paper is restricted to this alloy.Studies of the In 718 alloy subjected to the VAR process have established that melt rate M (kg/hr) depends not only on the melt current 1m (kA) supplied to the furnace, but also on ambient gas pressure of CO, PCO (micron), and electrode gap ge (mm) as well (1):"

Jan 1, 1986

By K. Ohmori, K. Takeya, S. Yoshizawa, A. Kawamoto, T. Ishikawa

"High performance Sm2Fe17N3 magnet powder is developed nitriding Sm2Fe17 alloy that 'is made using a reduction and diffusion method. Typical remanence, coercivity and maximum energy product of the fine powder are 1.40 T, 1.13 T and 323 kJ/m3, respectively. Decreasing samarium content, oxygen content and the amount of a-Fe are found to be the important factors to realize high-energy product.High performance injection molded Sm2Fe17N3 anisotropic magnet is also developed using the powder and an original binder system developed in order to mold at low temperature. Typical remanence, coercivity and maximum energy product obtained are 0.77 T, 0.78 T and 103 kJ/m3, respectively in the density of 4.77 Mg/m3The temperature coefficient of remanence is -0.07 %/K and that of coercivity is -0.54.%/K. The initial irreversible flux loss of the magnet that has a permeance of two is -5 % at 100 °C and the irreversible .flux loss of it is -4.4 % exposing it at 80 °C for 1000h.IntroductionSm2Fe17N3 alloy powder is expected to be very useful for a bonded magnet. The reasons are as follows. The magnetization is as large as the Nd2Fe14B alloy. Curie temperature is even higher than the alloy. The uni-axial anisotropy is comparatively higher than the alloy. Consequently it is possible to obtain high coercivity after just milling the powder and therefore possible to obtain high-energy product in a bonded magnet as it is realized in the SmCo5 bonded magnet. On the other hand, sintering is difficult because it will be decomposed into samarium nitride and a-Fe when heating it up to 500°C:"

Jan 1, 2000

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 Christine Wenzl, Andreas Filzwieser, Stefan Konetschnik

"The METTOP-BRX-Technology is a novel manifold electrolyte inlet, which allows improved productivity and production in new and existing tankhouses by achieving higher current efficiency and cathode quality, as well as using current densities higher than 400 A/m2. Two installation examples are shown: Montanwerke Brixlegg AG, Brixlegg, Austria (upgrade of existing tankhouse) and Xiangguang Copper, Yanggu, China (new tank house). Montanwerke Brixlegg AG has been using the METTOP-BRX-Technology since 2005, and converted half of the whole tankhouse to METTOP-BRX in 2011 in order to use a current density of more than 400 A/m2. Xiangguang Copper started up their second tankhouse in May 2011. This tankhouse was constructed in the same way as the existing tankhouse, but was designed for 292,000 t/a cathode copper (existing tankhouse: 200,000 t/a) by using the METTOP-BRX-Technology. This production increase is a consequence of a much higher current density, namely 410 A/m2, compared to 280 A/m2 in the old tankhouse.IntroductionCopper electrorefining has been practised for more than hundred years, the last big change being the implementation of stainless steel cathodes in the 1980s [1], In 2005, the METTOP-BRXTechnology was first introduced. This technology was developed jointly by METTOP and Montanwerke Brixlegg, Austria, and allows improvements in productivity and production in new and existing tankhouses in an economic way. The METTOP-BRX-Technology is a novel manifold inlet that allows improved tankhouse productivity by increasing current density and/or current efficiency while maintaining or improving cathode quality [2]."

Jan 1, 2012

By A. René Silva

The separation of Fe(III) from simulated Ni(II) solutions using different ion exchange resins was studied. The resins tested included cation exchangers with sulfonic and carboxylic groups and chelating resins with iminodiacetic, aminophosphonic, and mixed sulfonic and phosphonic groups. The dosage of resins was varied from 0.1 to 0.5 g/mL to study the impact of resin type and dosage on iron separation from simulated nickel leach solution containing 25 g/L Ni(II) and 25 g/L Fe(III) at pH 1.5. Also, the effects of different metal ion concentrations, Fe (III):Ni(II) ratios in solution, pH, and adsorption times were investigated. Experimental results demonstrate that all the chelating resins selected favored the adsorption of Fe(III) over Ni(II) with high Fe(III) loading. Soft cation exchange resins also favored the adsorption of Fe(III) over Ni(II), but no significant Fe(III) loading was observed. In contrast, strong cation exchange resins did not show adsorption preferences. The most efficient separation was observed using resin with aminophosphonic groups at resin dosage of 0.2 g/mL, having a Fe(III) adsorption over 94% and Ni(II) adsorption below 5%.

By Zhong g. Shui-ping

A new type Pb-Ag (0.8wt%)-Bi (0~5.0wt %) alloy used as anode in electrowinning of zinc from sulphuric acid electrolytes was prepared. The electrochemical properties of this ternary lead alloys have been tested and compared with those of Pb-Ag (0.8wt %) anodes used in industry. Results show the anodic overpotential decreases with the increasing of Bi content in the alloys. When the content of Bi was 1.0 wt% and 5.0 wt%, the anodic overpotential is about 40?50 mV and 60?80 mV lower than that of Pb-Ag (0.8wt %) alloy, respectively. The formation of oxide layers on the surface of these alloys was traced by LSV methods and the composition of the anodic oxide layers was characterized by XRD and SEM analysis. The surface layer on the two type anodes examined is mainly composed of a?PbO2 and ß?PbO2. But different structure of the surface layer was observed, Pb-Ag (0.8wt%)-Bi (1.0wt %) has a more fine-grained structure as compared to Pb-Ag (0.8wt %). But the film on Pb-Ag (0.8wt%)-Bi (3.0wt %) alloy is rather friable, cracked and not tightly attached to the anode.

Jan 1, 2008

By Ann M. Hagni

The mineralogical, chemical, microtextural, and particle size character of electric arc furnace (EAF) dusts are being studied by reflected light microscopy, scanning electron microscope-energy dispersive spectroscopic analysis (SEM-EDS) and electron probe microanalysis (EPMA). The dusts consist predominantly of metallic iron, iron oxide, and calcium-iron-manganese silicate phases, together with smaller amounts of iron-manganese-zinc-calcium, iron-calcium-zinc-manganese, and calcium-iron-manganese silicates. The samples vary in their zinc contents. Chlorine occurs in phases containing iron, lead, zinc, manganese, and calcium. The dust particles range greatly in size from 1 to more than 300 ~m, but most particles are about 1 to 6 ~m. Larger particles. about 20-50 um across. also are present. They are predominantly spherical in shape, but some are cenospheres, and others are more angular particles, some of which are broken spheres and cenospheres. Their internal microtextures exhibit evidence of liquid immiscibility, exsolution, skeletal crystal growth, and oxidation react i on rims. Because EAF dusts have been classified by EPA as hazardous wastes, there is heightened interest in the treatment of these dusts to render them non-hazardous. The mineralogy of products of pyrometallurgical treatment of EAF dusts by flash furnace and pyrohydrolysis are currently under study.

Jan 1, 1991

By Zhi-xiang Cui

Effects of flux, vulcanizing agent and reductant on slag cleaning in new-type slag cleaning furnace (Φ3.6 × 8.1 m) were investigated under the conditions including smelting temperature of 1200 and 1250 °C, settling time of 30 and 60 min, and Fe/SiO2 of 1.7–1.9. The results show that addition of SiO2, B2O3 or CaF2 into original copper smelting slag can improve settling separation effect. Though no effect on copper recovery, addition of FeS can provide heat required by reaction with oxygen and reduce copper dissolution in spinel phase and slag. Copper content in discarded slag can be controlled at 0.26% under the optimum comprehensive conditions with ratio of oxygen to natural gas of 1.6.

By J. N. Kondo, M. Hara, T. Smida, N. Ooto, K. Domen

"A porous material composed of two-dimensional anionic sheets of a layered perovskite, KSrNb30 10, was studied as photocatalyst for the production of Hz in the presence of alcohol sacrificial donors. Colloidal single and multi-layered HSr2Nb30 10 sheets were formed by intercalating ietra(n-buthylammonium) cations into the interlayeres of H+-exchanged KSr2Nb30 10 (HSr2Nb30 10), and addition of HN03 solution to the colloidal suspension precipitated the porous materials in which HSrNb30 10 sh~ets rand~mly stuck together. Original HSr2Nb30 10 before exfoliation had a BET surface area of 1 m2 g-1, whereas the surface area of a porous material prepared under optimal conditions exceeded 100 m2 g-1. The porous HSr2Nb30 10 had considerably higher photocatalytic'activitie8 for oxidation of 1-propanol and 1-buthanol than HSr2Nb39io, indicating that in the porous materials many niobate sheets are available for decomposition of these large alcohols.IntroductionQuite a research effort has gone into the design and study of porous materials. Such materials with large surface areas would have applications in highly efficient adsorbents or catalytic reactions.We have been studying photocatalytic reaction by cation-exchangeable layered metal oxides, where alkali metal cations are intercalated into the interlayers of inorganic sheets.[1,2] There are several advantages to using layered compounds rather than bulk powders for photocatalysis. Layered compound is rich in variety, in addition, modifications of them are easily performed by exchanging alkali metal cations in the inter layers for H + or other metal cations. The most important advantage is that some layered compounds have considerably high photocatalytic activities than bulk catalysts because the electrons and holes generated in each thin inorganic sheet readily reach interlayer spaces as reaction sites at the illterlayer spaces. It should be very important for further improvements· of layered photocatalysts to utilize two-dimensional inorganic sheets effectively."

Jan 1, 2000

By R. Padilla

The reaction of chalcopyrite with gaseous sulfur has been investigated in the range 350-450 °C in order to transform this mineral into a more acid soluble copper sulfide and insoluble iron sulfide. The results of thermodynamic analysis of this system as well as the X-ray diffraction analysis of the reaction products showed that in the temperature range 350 400°C the sulfidation reaction proceeded without formation of intermediate copper-iron sulfides according to: The effects of temperature and time on the conversion of chalcopyrite were studied. Conversion of chalcopyrite reached about 80% very rapidly with increase in temperature up to about 400°C. The recovery of copper from the sulfidized samples was determined by leaching in oxygenated 1.2M H2S04, 2M NaCI solution. Copper recoveries over 90 % were obtained from samples sulfidized for 30 min at temperatures lower than 400°C.

Jan 1, 2001

By Tomoji Kawai

"The Pulsed Laser Deposition method using multi-targets is extremely useful for the creation of functional multi-layers and variety of artificial lattices. The topic of the present talk is on the creation of ''Function hannonized artificial lattices by laser ablation"" made of the combined magnetic, ferroelectiric and superconducting layers. The outline of talk is,1. Features of Pulsed Laser Deposition method (Laser Molecular RHEED and S1M/AFM.2. Creation of magnetic, dielectric and superconducting artificial lattices by Pulsed Laser Deposition.3. Novel properties of function harmonized artificial lattices: especially on the magnetic and magnetoresistive artificial The outline of talk is, lattices made of3d transition metal oxides."

Jan 1, 2000

By A. Deepatana

Bioleaching of nickel laterite ores is based on the use of heterotrophic fungi organisms and their metabolites (organic acids) to dissolve nickel and cobalt from oxide minerals to form metal-organic complexes. Metal recovery from this process using an aminophosphonic acid based chelating resin (Purolite S950) was investigated as a function of metal concentrations, complexing agent including citric, dL-malic and lactic acids. Batch adsorptions were conducted using synthetic leachate solutions of nickel and cobalt with concentrations from 15 to 2000 mg/L prepared in 0.01 and 0.1 M organic acids. Adsorption equilibrium data were interpreted using the Langmuir, Freundlich and Dubinin-Kagner-Radushkevich (DKR) models. The results showed that equilibrium adsorption data for nickel-organic complexes followed the Freundlich model and those for cobalt agreed with the Langmuir model. It was observed that the maximum adsorption capacities of nickel and cobalt were 3.26 and 10.48 mg/g resins respectively. These were achieved in metal complexes prepared from 0.01 M lactic acid. Metal elution was conducted using 2 M nitric acid. High metal recoveries were achieved from low metal concentrations but were found to decrease with increasing metal concentration. The results suggest that effective recovery of nickel and cobalt from low concentration of metals, such as those generated from bioleaching operations, can be achieved suitably using chelating resins.

Jan 1, 2006

By M. Urda-Kiel

Stainless steel is increasingly used as a cathode starting sheet. It was shown earlier that even when depositing copper on copper, a substrate-influenced zone appears in the deposit structure, followed by a transition zone and finally by the electrolysis-influenced structure. On copper, the substrate-influenced zone has a thickness of twenty micrometers and on titanium, eventually more than fifty micrometers. Initial nucleation and growth have a considerable influence. In this paper, copper was deposited in a channel cell on four different 304 stainless steel substrates: mechanically polished and anodized, respectively, at 0, +400 and +800 mV/SHE in 1M H2SO4 at 20°C. Copper was deposited under electrowinning conditions after solvent extraction (SX) (40 g/l Cu++, 180 gh/l, H2SO4, 20 or 60°C). The results showed that, although Auger surface analyses of the substrates were only slightly different one from another including the oxide thickness, nucleation and initial stages of growth were very sensitive to the surface treatment of the substrate. Potential step and current step methods gave similar results : progressive nucleation followed by 3D diffusion controlled growth. The highest nucleation frequency was observed on stainless steel anodized at 0 mV/SHE, under various electrolysis conditions. The potential influence of these findings on industrial practice is discussed.

Jan 1, 1999

By S. N. Ashrafizadeh

Nowadays, hard carbides have found various industrial application in the manufacture of cutting and drilling tools as well as metal forming devices. About 60% of the world tungsten production is consumed in the manufacture of hard carbide pieces. Regarding the high economic value of hard carbide components, i.e., Ni, Co, TaC, TiC, and WC, their recovery from scrap species is attracting much interest. In the current research, the cobalt and tungsten content were recovered from scrap cemented carbide pieces through the application of high voltage electrolysis in nitric acid media. By this method, cobalt and tungsten were initially recovered as cobalt nitrate and tungstic acid, respectively. The precipitate of tungstic acid was calcined at 800ºC after being washed twice with distilled water. A pure tungstic oxide was obtained. The effects of current density, electrolyte concentration, speed of agitation, and the surface area of the anode on the efficiency of the electrolysis process were investigated. The optimum conditions of current density of 1500 A/m2, an acid concentration of 1.5 M, and a cell temperature in the vicinity of 60 to 80ºC were obtained. At the optimum conditions, an acceptable rate of collapse for the anodic carbide pieces of about 3.1 g/h was achieved, which remained constant up to the completion of the recovery process without any passivation .

Jan 1, 2003

By Chen Chen, Wang Yanze, Hong Xin

Furnace superalloy was applied in harsh environment within the erosion of high temperature and oxidizing atmosphere. With plasma powder surfacing technology, iron-based alloy powder was sprayed on the surface of 310S stainless steel to form oxidation layer that increases the oxidation resistance and reduces the cost of materials. With optimum technological parameters, in this paper, oxidation test of 100 hours on iron-based cladding alloy and furnace alloy were carried out at 1200 . The technique of XRF, XRD and EDS were used to characterize composition, oxide morphologies and surface mechanical properties. The results showed that Element composition of cladding layer formed by Plasma powder surfacing was well distributed. Its oxidation weight gain rate of 100 hours was 0.4552g/m2h, belonged to antioxidant level. The oxidation weight gain rate of furnace alloy was 1.4617g/m2h, belonged time-antioxidant level. And on the mechanical comparison test, surfacing alloy is relatively excellent than furnace alloy.

Jan 1, 2016

By Gerardo Fuentes

The stoichiometry and kinetics of the hydrothermal reaction of enargite in copper sulphate solutions was investigated in the range 140–300 °C, and particle size under 15 and 50 μm. The stoichiometric experiment was performed at 300 °C, using one gram of sample (96% enargite, 4% tennantite) and 100 mL of copper sulphate solution (10 gpl) at 1.2 pH. Enargite reacted completely after 80 min. A solid product was obtained and characterized by XRD. The main product was chalcocite (M) and some traces of djurleite and chalcocite (Q). Tennantite did not react under these conditions. The kinetic experiments were conducted at 140 °C, 190 °C, 250 °C and 300 °C. From fitted data and Arrhenius equation the calculated activation energy (Ea) was 51 kJ/mol. According to the hydrothermal transformations studied, the reactivity of different phases found in the copper concentrates was bornite > chalcopyrite > covellite > sphalerite > pyrite > enargite > tennantite.

By Chai Liyuan

This paper focused on the preparation of porous ceramic pellets for microorganism carriers. A new method for the process was developed using simple gel-casting and bubble-in-water-in-oil type of multiphase double emulsion. The globules, consisting of a foamed sepiolite slurry suspension, were dispersed and consolidated in spherical shape in liquid paraffin as gelation progressed. The green pellets were sintered at 1100°C. The influence of surfactants, extension ratio and impeller revolution rate on the process and characteristics of the pellets was investigated. The pellet size was in the range of 1~4mm and determined directly by impeller revolution rate. The fine cell diameter of porous ceramic was in the range of 100~500m and the micropore diameter was less than 5m. The inner macropores were interconnected and extend to the external surface. It is impossible to analyze a result by SEM micrographs and digital camera.

Jan 1, 2006