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By Bradford C. Wesstrom, Omar Araujo

"Impurities from an electrolytic refinery are typically extracted from the electrolyte utilizing conventional electrowinning cells. These cells are arranged in series with cascading solution flow and are commonly referred to as liberator cells. The Freeport McMoRan Copper & Gold El Paso Refinery has optimized the removal of arsenic in cascading liberator cells by utilizing two separate feed solutions. The primary feed solution is recycled liberator electrolyte and the secondary feed solution is ""neat"" tank house electrolyte. The secondary feed solution is added based on the voltage response across the individual cells utilizing independent variable frequency drive (VFD) pumps. When the voltage across a cell changes, a signal is sent to the VFD pump to maintain a cell voltage of 1.98 volts. By maintaining this voltage the copper content in each cell exits at 2-4 grams per liter. This safely optimizes the arsenic removal as copper arsenides on the liberator cathodes.IntroductionDuring the electrolytic refining of copper, impurities from the copper anode report both to the bottom of the electrolytic refining cell as slimes and to the electrolyte. The impurities which enter the electrolyte are arsenic, antimony, bismuth and nickel. The impurities that report to the electrolyte during the electrolysis process gradually increase. As these impurities increase, they are incorporated into the refined copper cathode. There are many processes that have been used to remove these impurities from refinery electrolytes. Some of them are listed as follows: solvent extraction, ion exchange, hydrogen sulfide reduction, bioreactor, adsorption onto a low - solubility metal-oxide hydrate, adsorption onto activated carbon and EMEW cells. The conventional process used by the copper refining industry for controlling the level of impurities in electrolyte involves multistage electrolytic cascading liberator cells. In these cascading liberator cells copper, arsenic, antimony and bismuth are removed as various mixed deposits from the electrolyte. Removal of these impurities is achieved through an increase in voltage resulting from the depletion of copper in the electrolyte through electrowinning. With this higher voltage, the Group Vb elements, arsenic, antimony and bismuth are deposited on the copper cathode and report as slimes to the bottom of the cells. Nickel is removed in a subsequent process."

Jan 1, 2012

By Kimio Ilagaki

The distribution ratios of Ag, Pb, As, Sb and Bi for the Cu2S-FeS or Ni3S2-FeS matte I FeOx-SiOl, FeOx-Si02-CaO or FeOx-CaO slag equilibration in a MgO crucible were determined experimentally at 1523 ~1573K under controlled partial pressures of S2 and 02 at given PS02 of 10.1,50.7 and 101.3 kPa(O.I, 0.5 and I atm), and the observed dependency of distribution ratio on the matte grade, S02 pressure and slag basicity were analyzed on the basis of thermodynamics.

Jan 1, 2003

By M. Hashiuchi

In 1972, the tankhouse of the Tamano Smelter adopted a high current density electrolysis operation applying the PRC (Periodic Reverse Current) method. In 1994, the phase four production expansion project, which incorporated significant re-structuring of the organization, was completed and we have achieved an annual production capacity of 191,000 tons. The target of this project, the production capacity, was increased by 1'8% and labor productivity by 25%. After the expansion, some improvements in the starting sheet section and the verticality of the electrodes were carried out, and the efficiency of the operation was greatly enhanced, including the improvement of the quality of the electrolytic copper.

Jan 1, 1999

By Tianyou Huang, Yuan Lu, Haimin Long, Jinwu Kang, Gang Nie

"The distortion of metal parts during heat treatment process is one of the main obstacles in industry to ensure high-quality work and less or no machining allowance, especially for large but thin steel castings such as heavy turbine blades. In the paper, a method is proposed to control the distortion by adjusting heat transfer coefficient of metal parts during heat treatment process. Required heat transfer coefficients can be realized by getting the metal parts into contact with various media such as water spray, insulation felt or materials with different heat conductivity. The control method based on this idea is set up and achieved. By using insulation felt and water spray to change the heat transfer coefficient during the stages of heat treatment process, the results indicate that the proper control time and vary with materials.IntroductionThe distortion of metal parts during heat treatment process is one of the main obstacles in industry to ensure high-quality work and to realize less or no machining allowance [1]. For example, the Three Gorges turbine blade’s distortion is as large as 50mm during heat treatment process. The uneven heating and cooling during heat treatment process is the main reason for distortion [2]. By adjusting heat transfer coefficient of different areas of metal parts, the heat treatment process could be controlled. The temperature variation, direct cause for distortion, could be under control. Loeser Klaus used high pressure gas to achieve uniform heat transfer during gas quenching and proposed the possibility to use ""Dynamic Quenching"" processes where the quenching severity is varied during quenching by stepwise control of either gas velocity or gas pressure [3]. Li Zhichao also suggested minimizing distortion by marking a component into several areas and imposing different heat transfer coefficients on each area [4]. Heat transfer coefficient can be controlled by getting the metal parts into contact with different media such as water spray, insulation felt, air or different heat conduction materials. In addition, the exact time to adjust the heat transfer coefficient is another factor for distortion. A method is presented in this paper by actively adjusting heat transfer coefficient for different areas of metal parts and different stages of heat treatment process to control their distortion. The corresponding experiments have been made by using different metal materials."

Jan 1, 2012

By Byung-Young Choi

Nitrogenated carbon films were deposited on the high-frequency induction hardened steels by ion beam assisted deposition. X-ray photoeleetron. spectroscopy and scanning electron microscopy were used to analyze the chemical content and the morphology of the coated steels. Rolling contact fatigue tests were performed using Polymet RCF-1 machine with a constant supply of lubricant. It was found that CNx films adherent to the steels substrates were formed by ion beam assisted deposition. It was also found in the rolling contact fatigued specimens that non-propagating crack was initiated in the white etching area indicating the maximum shear stressed, region, leading to surface failure.

Jan 1, 2000

By K. Morsi, P. Mehra

"Spark plasma sintering has gained a considerable amount of attention over the past decade, due to its rapid sintering rates, and low temperature requirements, but has so far been usually limited to the production of simple geometries. The present paper examines the current-activated production of extended geometries through the process of spark plasma ""extrusion"". Of interest in the present study is exploratory research into the effect of electrical current activation on the reactive consolidation of powder systems to form intermetallic materials.IntroductionSpark Plasma Sintering (SPS) has been the subject of intense research over the past decade [ 1,2, 3,4,5,6]. The process boasts unique advantages which include ultra fast heating rates, shorter sintering times and lower sintering temperatures than needed in conventional sintering. The process is however limited to the generation of predominantly simple geometries. Recently one of the authors investigated the spark plasma extrusion of aluminum, where an aluminum powder compact is directly (Joule) heated through an applied DC electric current. Here extended geometries can be generated under the influence of electric current. A number of heating sources were identified including the heat source from current, i.e. Joule heating, frictional heating and heat from the deformation energy. However in the case of reactive powder systems, an extra ""one-time"" transient heating source can be supplied. By considering combustion synthesis of powders, this heating source is derived from the reaction between elemental powders to exothermically form a product at some ignition temperature [7]. This exothermic energy heats the compact to the maximum ""combustion temperature'', which could be hundreds of degrees higher than the ignition temperature. Hence a high temperature processing window (of short duration due to heat losses to the surroundings) becomes available in which the material is most suitable for stress-induced deformation and consolidation. For reactive spark plasma extrusion, two scenarios can be envisioned. The first is where the reactive powder compact is ignited through the application of current, and extruded within the high temperature processing window (also under the influence of current). The second scenario is to allow the heat of deformation/friction to heat the material during extrusion, to simultaneously force a reaction and consolidation. Here it is expected that the processing window will be very small if feasible."

Jan 1, 2011

By Ruixiang Wang, Jinhui Li, Youjun Xiao, Daoling Xiong, Hao Chen

"Leaching solution prepared from spent battery materials contains large quantities of valuable metals, such as Cu, Ni, Co, Mn and Fe. Therefore, recovery of valuable metals from acidic polymetallic aqueous solutions is of great importance for every plant. In this work, a method is introduced of recovery of Ni, Co and Mn from polymetallic solution prepared by leaching spent battery material. The basic concept includes copper was removed through replacement by iron powder followed by iron precipitation in goethite method. The experimental results show that Cu can be removed 99% at least through replacement by Fe powder, and the removal of Fe can achieve 99% by goethite method. At the same time, the loss of Ni, Co and Mn are about 2%, 3 % and 2%, respectively. The process of differential removal of metals can be selected as the treatment alternative that combines simplicity, efficiency and reliability with low capital and maintenance costs. The purified solution which only contains Ni, Co and Mn can be used to prepare NixCoyMnz ternary system precursor.1 IntroductionNickel and Cobalt are very important metals which are applied in many fields, such as energy material and support material for some new material field. The world demands for such metals is progressively increasing, while raw resources are being depleted and with the constraints raised by the Law and related legislation assigned to protect the environment from hazardous wastes in the world. Nowadays study on reutilization of waste materials has great significance for achieving secondary resources recycling and preventing environmental pollution. There are many hydrometallurgy methods applied for dealing with these wastes, while they usually contain large quantities of valuable metals, such as Cu, Co, Mn and Ni, as well as impurities, such as Fe, Zn, and etc. Therefore, proper treatment of these leaching solutions prior to their discharge is of great importance, so that the contained valuable metals can be recovered.Separation and extraction of metals from leaching solution can use some methods through solvent extraction[l,2], ion exchange[3,4], precipitation with sulfide[ 5] or alkali[ 6] and electrolytic recovery[?]. Among the appropriate treatment alternatives, replacement and differential precipitation is the most attractive treatment that combines simplicity, efficiency and reliability with low capital and maintenance costs."

Jan 1, 2011

By Tian Tang, Sergio D. Felicelli

"The laser cladding is an important surface treatment for enhancing resistance against corrosion, abrasion, and wear. The focus of the present study is to develop a three dimensional finite element model to analyze the temperature history and thermal stress evolution during multi-pass laser cladding process on H13-H13 tool steel sample. A sequentially coupled thermal-stress analysis methodology was adopted in this study. The thermal model was firstly established to investigate the temperature history of the laser cladding process. Then the temperature history was used as input to mechanical model to calculate the thermal stress evolution during the process and the residual stress after the sample completely cooled down to room temperature. The influences of process parameters including the scanning speed and scanning strategies on temperature history, thermal stress evolution, and residual stress were investigated in details.IntroductionLaser cladding is an advanced material process technique, which is often used to improve mechanical properties or increase corrosion resistance, repair worn out parts, and fabricate metal matrix composites. In this process, the injected powder or wire feedstock material and a thin layer of substrate are melted and consolidated by use of a laser in order to coat part of a substrate or fabricate a near-net shape part.Numerous mathematical models have been established for analyzing the effects of process parameters, microstructure evolution, and thermo-mechanical behavior of laser cladding. Zhou et al. [1] established an analytical model to investigate the laser induction hybrid rapid cladding for Ni-based WC composite coatings. Huang et al. [2] also developed an analytical model to theoretically investigate the interaction between the laser beam and the powder stream of laser cladding process. A simple and realistic model of laser cladding was proposed by Picasso et al. [3]. The cladding layer is very sensitive to cracks due to the accumulation of residual stress, caused by non-uniform temperature changes, which have limited the wide application of laser cladding technique in industry. Recently, fmite element method has been increasingly used to simulate the laser cladding process [ 4-6]."

Jan 1, 2014

By James C. Foley, David K. Rehbein

"In-situ characterizations of green state part density and sintering state have long been desired in the powder metal community. Recent ·advances in non-contact electromagnetic acoustic transducer (EMAT) technology have enabled in-situ evaluations of the acoustic attenuation and velocity as sintering proceeds. Pure aluminum (99.999%) and aluminum alloy powders were prepared with high-pressure gas atomization (HPGA). The powders were pressed in a uniaxial die and examined with acoustic waves for changes in velocity and attenuation during sintering. The changes in acoustic properties were correlated with sample microstructures and mechanical properties. Evolution of the acoustic echo train during sintering is shown to provide information on the state of sintering as well as having the potential for detection of interior flaws.IntroductionThe versatility of powder metalallurgy (PIM) technology in the manufacture of complex shapes has enabled an increasing amount of wrought and casting production capacity to be converted to PIM technology. However, ultrasonic inspection of green components produced using PIM techniques remains a challenge and is not generally practiced [1]. Inspection of PIM components in the green state is highly desirable, because the green part can be reclaimed with only accepted components being subjected to further costly processing. Another potential benefit is characterization and greater understanding of the sintering process itself. An increased scientific understanding of the sintering process enables intelligent process control, greater reliability of the production process and a lower rate of rejection of the finished product. In order to realize these potential benefits, it is necessary therefore that accept/reject criterion be based on real time nondestructive evaluation of the green-state components and the sintering process.Most current nondestructive inspection techniques suffer from their inability to perform inspections below the near-surface region with the exception of X-ray and to some extent pulsed eddy current [2]. X-ray inspection requires extensive shielding of production personnel and expensive film and film processing. While development of pulsed eddy current techniques have lessened the impact of the well-known skin effect, the depth of penetration of the induced eddy currents remains somewhat of an issue [2]."

Jan 1, 2000

By A. Mikula, S. Karlhuber

"Unique physical and mechanical properties made the Pb-Sn solders attractive for low temperature joining of electronic parts. But since lead in solder materials has become a great enviromental problem and health concern, lead will be slowly replaced by other materials in soft solders. Some of these materials which are currently under investigation are ternary tin alloys. Many different physical properties like wetting behavior, electrical and thermal conductivity and surface tension are measured on these alloys, but on the thennodynamic properties and the phase diagram of the alloys under discussion there is only little information available. We investigated the (Ag, Au, Cu)-Sn-Zn systems and determined the thermodynamic properties over the whole composition range by emf-measurements. From these measurements we also got some information on the liquidus. In the Sn-rich corner the phase diagrams are still under investigation.IntroductionSoldering is technically defined as the joining of two base materials, mostly metals or metal coated nonmetallic substrates, with a third metal. The melting temperature of the third metal or metal alloy should be well below those of the substrates. Solder alloys can be categorized in soft and hard solders. Soft solder alloys usually contain lead, tin, bismuth, indium or cadmium and hard solders gold, zinc, aluminium or silicon. The difference between soft and hard solders is the melting temperature of the soldering material. This temperature is around 350°C.An interesting brief history of solders is given by Vianco and Frear [1]. They report, that in 4000 B.C. solders were already used in Mesopotamia. From archaeoligical evidence those solders were gold-based hard solders.Tin-lead soft solders and their use are not easily found, because in course of time tin has been reduced to stannic acid, making the identification quite difficult. Well preserved soft solder artifacts were discovered in King Tut's tomb dating from 1350 B.C. In ancient time Pb-Sn solders were used primarily for the manufacture and repair of cooking utensils and metal tools. The Romans used lead-tin solders extensively in the construction of the aqueducts."

Jan 1, 1996

By K. B. McTaggart, G. Owusu, P. J. Merrin

"This study was conducted at Hudson Bay Mining and Smelting's zinc electrowinning tankhouse to determine the effects of varying levels of antimony and continuous gelatin addition on current efficiency. The levels of antimony and gelatin were varied from 0.012 to 0.030 mg/l and 0 to 10 mg/ll2 • 31 respectively, based on neutral ZnS04 electrolyte. A non-linear mathematical model relating current efficiency with antimony and gelatin was produced. The optimum operating point for gelatin was 6.5 mg/l. On the other hand the current efficiency increased with decreasing antimony levels. An interaction term between gelatin and antimony is present but is not significant enough to improve the ability of the tankhouse to handle purification upsets in antimony. Individually, the current efficiency was linear (decreasing) with antimony, and parabolic with gelatin concentration. However, at low antimony concentrations stripping of the cathode sheet was difficult. IntroductionThe zinc electrowinning tankhouse at Hudson Bay Mining and Smelting was designed in the 1930's and consists of 120 rows with each row containing ten cells. This system cascades acid from cell to cell In a row, with neutral zinc sulphate solution added to each cell through manually controlled spigots. Animal glue additions are made manually three times per day by operations personnel. The problem with this type of cell design and operation is that feed solution flows and composition can vary from cell to cell and from row to row due to the large number of manual control points. A new system which reduces the number of manual control points was designed and tested to determine if improvement in control of cell conditions would affect current efficiency. This system mixes spent acid, neutral ZnS04 electrolyte and reagents (gelatin, antimony and strontium carbonate) in a separate mix tank, ensuring that all cells receive a uniform feed solution. Gelatin was used in the test system instead of animal glue (which is presently used) because of the poor solubility and supply of industrial animal glue. The study reported here is the first in a series of experiments designed to justify the need to modify the present cascading cell feed system (Figure 1) to the proposed feed system (figure 2)."

Jan 1, 1997

By Z. Smieszek, Z. Szota, P. Gajowski

"A new method for measuring the total quantity of suspensions contained in the electrolyte during copper electrorefining has been developed by the Institute of Non-Ferrous Metals, Gliwice. Electrolyte purity, and the suspensions content in particular, is of essential importance for the quality of electrolytic copper produced during the process. Suspensions contribute to the increase of slime impurities in electrolytic copper and increase losses in noble metals. Up to now, the laboratory method has been used for the· process control which provides analytical results with considerable time delay. Therefore, it is useless for the process control.The measuring method developed enables continuous measurements of a suspensions content directly within the stream of the flowing electrolyte. The principle of measurement is based on changes in optic properties of the electrolyte with varying suspensions content.1. IntroductionIn copper electrorefining, it is essential that the final product quality be maintained. If suspensions are present in electrolyte, the content of slime impurities in electrolytic copper, (such as Pb, Ag, Bi, Sn, Sb, and As), increases which can result in the occurrence of the so-called slime dendrites on cathodes, thus debasing the quality of the product. As a normal suspension content in electrolyte, the contents in the order of several mg/l are considered, usually not more than 5-6 mg/l, while contents exceeding 20 mg/l are referred to as an alarm state. Suspensions present in an electrolyte are usually a light fraction of anodic slime whose main components are metallic silver, lead sulphate, complexes of antimony and arsenic, and sometimes even calcium sulphate; they are mainly composed of very small particles of lead sulphate and antimony complexes. Sometimes - - in case of alarm states - - the so-called ""wandering slims"" can be observed, which are composed mainly of arsenic and antimony complexes. These ""wandering slims"" make a serious technological disturbance. In normal operating conditions of the electrorefining plant, an increase of suspension content can result from such reasons as crack of filter cloth in a slime filter, turbulent flow of the electrolyte, anodic passivation, aeration of the electrolyte, and improper servicing of an electrolytic tank. It is necessary to continuously control the suspensions content in electrolyte for proper electrorefining."

Jan 1, 1989

By Reuben John Mathew

"Oxygen evolution is the main anode reaction in industrial copper electrowinning. The oxygen bubbles do not conduct electricity, thus increasing the electrolyte resistance. The oxygen bubbles formed at the anode rise to the surface, occupying a larger volume of the electrolyte at the top of the cell than at the bottom. This oxygen bubble concentration gradient contributes to a gradient in electrolyte resistance and consequently a tendency toward uneven current distribution. This phenomenon increases the chance for uneven growth on the cathode and/or short-circuits, particularly on the lower portions of the cathode. This issue may be ameliorated by increasing the charge transfer resistance for oxygen evolution down the height of the anode. This concept was studied by solving the current distribution for a 2-D model of a copper electrowinning cell using COMSOL.IntroductionA copper electrowinning tankhouse aims to operate at the highest current density that will deposit on the cathode a layer of copper metal possessing the desired physical and chemical characteristics. The operating current density is directly related to the physical nature of the copper deposit on the cathode (Figure 1), limiting a copper electrowinning tankhouse to some operating current density that produces acceptable copper deposits.[!] The ratio of the operating current density to the limiting current density is typically around 0.3.[2] If the limiting current density for a cell could be raised, the operating current density could also be raised and thus result in savings in capital cost for a tankhouse. [3]The average operating current density in a copper electrowinning plant is 270A·m- 2 .[4] The value for average current density, however, obscures the fact that the face of a cathode does not experience this value equally. Indeed, the current density varies along the height of an electrode and is independent of the height of the electrode.[5] This phenomenon partly explains why the lower portions of a cathode tend to display a rougher copper deposit.In order to utilize a higher operating current density but still remain at 30% of the limiting current density, the limiting current density must be raised, but it is affected by the mass transfer regime at the electrodes. The mass transfer regime is currently poorest at the lower portions of the cathode and this is part of the reason for the tendency for poor cathode deposits to occur at the lower portion of the cathode.[6]"

Jan 1, 2012

By Hanlu Xie, Liang Yu, Ping Wang, Yuanchi Dong

"The leaching process is the first step when recycling BF slag as raw material for some other products. While studying the kinetics of the BF slag leaching process, a fractal phenomenon was found, which indicated some interesting mechanism in the process. The result suggested a new understanding of the leaching process in detail which useful for the industrial applicationIntroductionTypical composition (wt. %) of blast furnace slag varied in a pretty wide range: SiO2 30–40, Al2O3 10–20, CaO 30–40, MgO 5–10.The ground granulated slag is commonly used as base of roadway (mixed with natural inert for paving, soil stabilization, etc.) or one of the resources of Portland cements because of its good hydraulic activity [1]. To recycle the slag economically, the selective recovery of some components of the slag may be considered. As main components exist in the slag, silica [2, 3 and 4] and alumina [4] recovery was first considered.While recovering of silica from the slag, silica gels are recovered selectively from the leaching solution deriving from the treatment of the slag with waste sulfuric acid. After separation of the exhausted solid of leaching, the silica gel is precipitated from the solution at pH 3.2. Although the silica gels obtained by this procedure contain many impurities and need some more work afterward, it is the first and important step for the process.In the prior work [5], silica extraction using blast furnace slag had been investigated, focused on the pH value of selectively silica extraction. In the present work, kinetics of the leaching process was focused. It is important to design an economical process.ExperimentalThe composition of the slag and the calcined gels has been determined by a LINK860 (Oxford Instruments, Oak Ridge, TN) energy dispersive spectrometer (EDS) in conjunction with a CAMBRIDGE S250-M2 (Cambridge Instrument Ltd., Cambridge, U.K.) scanning electron microscope(SEM). The leaching of slag and the precipitation of silica gels have been conducted at atmospheric pressure in a stirred reactor placed at temperature controlled by a heated water bath."

Jan 1, 2008

By Laurence G. Dyer, David G. Dixon, John Rumball, Maziar Eghbalnia, Edouard Asselin

"Linear scan voltarnmetry was used to determine the reactions that occur during the cyanidation of petzite (Ag3AuTe2). Gold oxidation in petzite requires more oxidising conditions than are required for pure gold, it also does not achieve the same current (related to reaction rate). Tellurium oxidation occurs at a similar potential in water and cyanide, but as a component of petzite is impeded somewhat in water, likely due to the stability of the precious metals. Pre-treatment of petzite to oxidise tellurium in the absence of cyanide prior to gold recovery appears to be at least moderately successful.IntroductionWhile gold occurs most prevalently in its native form, many other gold bearing phases appear throughout natural systems [I]. Tellurides are a common group of such minerals, many of which also contain silver, often existing in association with native gold deposits. The six major gold-bearing tellurides are calaverite (AuTe2), sylvanite [(Au, Ag)2Te4], montbrayite [(AuSb)zTe3], krennerite [(Au1-x, Ag,)Te2], petzite (Ag3AuTe2) and muthmannite (AuAgTe2) [2]. While several other phases exist they are much more complex (i .e. buckhornite), which dilutes and confuses the influence of each specific component. Studies of gold tellurides have predominantly focussed on calaverite as it is the simplest and most common phase, however petzite, commonly found in Australia and North America, is the focus of this investigation.Gold processing via cyanidation has been operated for more than a century and is a highly effective hydrometallurgical treatment of native gold deposits. However, some gold alloys such as tellurides have proven to be somewhat less responsive under the same conditions. Several groups have shown that gold/silver tellurides are amenable to cyanidation, but are significantly more refractory than native gold [3]. Pre-oxidation steps have been tested to remove constituents that would consume cyanide such as sulfides. Such species are also linked to the precipitation of oxidised telluriwn, forming a passive layer, further inhibiting gold recovery [2]. It is uncertain to the definite reasons underpinning the refractory nature of precious metal tellurides in conventional cyanidation."

Jan 1, 2012

By Y. H. Wang, S. Kou

"Three-dimensional weld pool convection was computer simulated using dimensionless variables. The electromagnetic force, the buoyancy force and the surface tension gradient on the pool surface were treated through the use of the dimensionless electromagnetic force, the Grashof number and the Marangoni number. Other typical dimensionless numbers such as the Prandtl number and the Peclet number were also used. The calculated and experimentally observed fusion boundaries were compared. The convection patterns were shown and the effect of the Marangoni number was demonstrated. IntroductionSeveral weld pool convection models have been developed by Oreper et al. (1,2), Chan et al. (3) and Kou et al. (4). These models describe two dimensional convection in stationary weld pools in a semi-infinite workpiece. Since the vast majority of arc welding practices involve a moving heat source and weld pool, and the workpieces are finite in thickness rather than semi -infinite, a 3-D convection model for a moving heat source and a workpiece of finite thickness is expected to be much more useful.Weld pool convection can strongly affect the structure and properties of the resultant welds. Variations in weld characteristics which are likely to occur from changes in weld pool convection are: weld penetration, macrosegregation, gas porosity, solidification structure, undercutting and surface smoothness. Apparently, the quantitative understanding of convection and heat flow in weld pools is of considerable practical interest. Mathematical models describing convection and heat flow in weld pools are essential, not only because of the quantitative understanding they provide, but also because of the difficulties associated with the experimental measurements of weld pool convection. These difficulties are mainly due to the fact that only surface flow, rather than the overall convection pattern in the weld pool, can be observed. In fact, due to arc glow even the observation of surface flow can be rather inconvenient."

Jan 1, 1986

By K. Morsi, S. K. Kassegne, A. El-Desouky, K. S. Moon

"Current Activated Tip-based Sintering (CATS) is a new process for the powder-based fabrication of macro, micro and possibly nano-scale features and shapes. This new and unique process enables selective sintering of powders by localizing electrically activated sintering conditions through a stationary or moving electrically conducting tip. We present preliminary experimental results on the effect of tip size in the CA TS process as well as the effect of initial powder particle size on the sintering behavior of nickel powder.IntroductionSpark Plasma Sintering (SPS) has been the center of attention of numerous researchers due its noticeable advantages over conventional sintering techniques such as rapid heating rates, lower sintering temperature and shorter holding times. Research on SPS has been applied on a wide variety of materials such as pure metals [ 1], ceramics [2], composites [3], nano-materials [ 4], biomaterials [ 5], shape memory alloys [ 6] and many other material systems. However, it has been mostly limited to bulk materials with simple shapes with a few exceptions ofresearch efforts where the effect of electric current was combined with metal forming processes such as spark plasma extrusion [7,8] and electric rolling of powders[9]. In this paper a novel process (Current-Activated Tip-Based Sintering (CATS)) is discussed where electric current and pressure are applied simultaneously through a small conducting tip (stationary or moving) over a conducting powder compact. This process has the potential advantages of sintering complex geometries with minimum energy requirements as unconventionally high current densities can be achieved due to the small contact area between the tip and the powder compact. Furthermore, by controlling the tip size, it can be possible to sinter features on the macro-, micro- and even nanoscales."

Jan 1, 2011

By Paul Pajunen, Michael Sheedy

"Acid separation using short bed ion exchange is a now well established technology in copper refinery tankhouses. Refinery bleed streams from liberator cells are treated by short bed systems to produce an acid-free byproduct stream that contains the bleed metals and valuable nickel salts. Removing the acid eliminates the need for a black acid evaporator and reduces the amount of sodium carbonate required in nickel selective precipitation processes. The recovered sulfuric acid can be recycled to the tankhouse. This same technology is routinely used to treat other acids such as hydrochloric, nitric, and hydrofluoric. In the case of hydrochloric acid, the process can selectively separate chloro-anionic complexes such as Zn, Pb, and Cu, which are then eluted with water. The acid recovery technology can also be closely coupled with ion exchange processes in order to minimize regenerant acid consumption. In many hydrometallurgical applications resin regeneration often requires an acid dosage multiple times the stoichiometric minimum. Coupling an acid recovery bed with the IX column allows recovery and recycle of the free acid in the spent regenerant, thus reducing the overall acid consumption to just slightly more than stoichiometric.Short Bed Ion ExchangeThe short bed ion exchange process has been extensively used in the metal finishing industries since the early 1970s [1,2]. Short bed systems have also been sold to primary metals producers for the separation of sulfuric acid from copper refinery bleed streams [3] and for the recovery of nickel and cobalt from plant effluent streams. This unique technology optimizes the ion exchange process and offers a number of significant advantages over conventional ion exchange. The principal features and benefits of this technology are presented below."

Jan 1, 2012

By Shuichiro Okada

Various efforts to reduce energy consumption and smelting cost are made at Tamano Smelter. Production of anode copper has been increased by about 30 % and energy requirement has been decreased about 50 % respectively. Challenges toward more higher goal are being continued. Details about the following are described in this paper. 1 Waste heat recovery Steam recovery at up-take of FSFE Heat recovery from waste gas of anode furnaces 2 Application of tonnage oxygen 3 Application of pulverized carbonaceous fuels to the flash smelting furnace with furnace electrodes ( FSFE ) 4 Application of computer control system to copper smelting 5 Improvement of the fugitive gas collecting system 6 Improvement of the mechanical tuyere puncher for the converter furnace

Jan 1, 1983

By Huaming Yang

The vanadium-doped SnO2 nanoparticle was synthesized by the co-precipitation reaction and subsequent calcination from the vanadium(III) chloride and tin(IV) chloride. The crystal size, pore size distribution, micrograph and properties of the nanocrystalline powders were examined by differential thermal analysis (DTA), thermogravimetric analysis (TGA), X-ray diffraction (XRD), desorption isotherm (Barrett-Joyner-Halenda method) and transmission electron microscopy(TEM). Thermal treatment of the precipitate powder at 600°C led to the formation of V -SnO2 nanoparticle of -10mm in crystal size. Most of the pores in the nanoparticle are about 5~15nm in diameter. Effect of doped vanadium on the crystal size of the nanopartic1e was discussed.

Jan 1, 2003