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By G. R. Palmer

The success of future electric vehicles will depend greatly upon the power supply choices made today. Research is presently being conducted by automotive engineers and electrochemists to determine what battery type may be the most promising. Not only are product production and application efficiencies being evaluated but also environmental concerns of reclamation and recycling. Rechargeable batteries using nickel-metal hydride electrodes are strong candidates for these electric vehicle applications. The U.S. Bureau of Mines is investigating hydrometallurgical technology that separates and recovers purified metallic components present in nickel-metal hydride battery scrap. Sulfuric, hydrochloric, and nitric acids are all capable of dissolving the battery electrode alloys given the proper operating conditions. Solvent extraction of the leach solutions using D2EHPA removes iron, and selective precipitation shows promise of recovering the other metals in the H2SO4 and HNO, systems.

Jan 1, 1994

By Aiyuan Ma, Kun Yang, Weiheng Chen, Jinhui Peng, Shiwei Li, Feng Xie, Libo Zhang

In this thesis, a new process of recovering zinc sulfide ores was developed. The novel synthetic coordination leaching process mainly included two steps: microwave assisted phase reconstruction and compound coordination leaching. By applying various techniques, such as chemical composition analysis, X-ray diffractometry (XRD) and Raman spectroscopy, it could be concluded that sulfide phases would directly oxidized to zinc oxides under the 500 ºC microwave roasting and adding 30% Na2O2. What’s more, zinc leaching rate reached to 61.16% within 2 hours. Compared to the current technologies, this procedure had the advantage of avoiding SO2 emission, high leaching efficiency, simple process, manipulate easily, and low cost, which could be expected tremendous application potentials.

Jan 1, 2016

By Jinjing Dua, Jun Zhua, Kuiren Liub, Bin Wang, Xiaolei Wua

V-Ti-Fe as hydrogen storage alloy was prepared by reducing metal oxides with a metallothermic reduction method. The deoxidation process of the V-Ti-Fe alloy was performed by electro-deoxidation and vacuum induction melting method, respectively. The results showed that the content of oxygen impurity can be controlled at about 0.2wt% after electrolyzing for 240min. Both the maximum values of hydrogen absorption capacity and the effective hydrogen desorption capacity are 2.65wt% and 1.01wt%, respectively. The deoxidization effect of vacuum induction melting process is more remarkable, with Ce as the reducing agent. It is found that Ce addition is beneficial for reducing the componential segregation, promoting the hydrogen absorption activation of V-Ti-Fe alloy. When m(Ce)/m(alloy) is up to 5%, the oxygen content has been reduced to 0.05wt% and the maximum hydrogen absorption capacity and the effective hydrogen desorption capacity are up to 3.36wt% and 1.85wt%, respectively.

Jan 1, 2015

By Toshiro Kuji, Masakazu Fujita, Tetsuji Saito

"The magnetic properties of the magnetic materials were deeply dependent on the microstructures. In this study, the novel technique to produce the desired microstructures in a controlled manner was proposed. The technique consisted of the production of the amorphous alloys and the control of the crystallization process. The technique was applied to improve the magnetic properties of Nd-Fe-B permanent magnets. The microstructural control of the magnets exhibited the excellently high energy-products of higher than 430 kJm-1. The relationship between the magnetic properties and the microstructures of the Nd-Fe-B permanent magnets was discussed.IntroductionThe intrinsic properties of the materials are basically determined by the properties of the constituent elements or the compounds. However, it is often noticed the difference between the observed properties and the theoretical values expected from the intrinsic properties of the materials. This indicates that the observed properties of the materials are determined not only by the properties of the constituent elements. In other words, the observed properties of the materials are also strongly dependent on the morphology of materials. This means that the microstructural control may creates a great improvement of the properties of materials.In Nd-Fe-B permanent magnets, the superiority arises from the uniaxial intermetallic Nd2Fe14B compound which has a large saturation magnetization and a high anisotropy field [1,2]. The magnetic properties of the Nd-Fe-B permanent magnets are dependent on the microstructure, that is, the size, shape and degree of the crystallographic alignment of the Nd2Fe14B phase. Currently, the Nd-Fe-B permanent magnets have been produced by either sintering or melt-spinning [3,4]. In the sintered magnets, alignment of the Nd2Fe14B phase is achieved by the prior green compaction of the crushed ingot powders in an applied magnetic field [3]. In the melt-spinning approach, alignment of the Nd2Fe14B phase is achieved by hot deformation [5]. Amorphous melt-spun ribbons are comminuted and then are consolidated into bulk form by hot pressing before hot deformation. As-hot-pressed magnets have randomly oriented Nd2Fe1~ grains [6]. Subsequent die upsetting of as-hot-pressed magnets gives rise to the crystallographic alignment of the Nd2Fe14B phase."

Jan 1, 1998

By Larry G. Twidwell

The removal of dissolved arsenic from mine waste waters utilizing a lime/phosphate precipitation technique has been studied on a laboratory scale at Montana Tech of The University of Montana and on a pilot scale at MSE Technology Applications as a wastewater treatment process potentially capable of removing dissolved arsenic to <50 µg/L. Arsenic bearing lime and lime/phosphate slurries were subjected to laboratory extended-time air-sparged aging for over four years. The lime slurries released their arsenic back into solution in a relatively short period of time, whereas the lime/phosphate slurries showed limited release of arsenic. The developed process has been pilot scale tested by MSE-TA for the EPA Mine Waste Technology Program on three waters, ASARCO smelter blowdown water, ASARCO thickener overflow water, and Mineral Hill Mine groundwater. The laboratory study results will be presented and discussed in this presentation. The pilot scale results will be presented and discussed in a companion presentation. Stability, Aging, Apatite, Johnbaumite

Jan 1, 2005

By John E. Litz

Metal-bearing flue dusts are produced by some ferrous and non-ferrous industries. Many dusts are being or can be treated for recovery of metal values. Operating and proposed flowsheets for the most common dusts are reviewed. Advantages, disadvantages, product marketability, and cost implications are discussed for each flowsheet.

Jan 1, 1992

By C. Acuna

The standard procedure of fire refining consists of sulphur removal via air injected through tuyeres, arsenic slagging via soda-lime flux and oxygen reduction by air or oxygen deficient air or a steam fuel mixtures. The use of porous plugs to stir with an inert gas has been mainly considered as a surface renewing agent that increases the product quality and shorten the refining cycle. In the present study the effect of the bottom stirring by nitrogen gas injection through porous plugs for the treatment of the crude copper in the range of 400-150 ppm sulphur, 3,000?2,000 ppm arsenic and 14,000-7,000 ppm oxygen content was investigated. The combined effect stirring-reducing, by the use of air or a steam fuel mixtures through tuyeres for oxygen removal, follows a kinetics of first order where the constant, K, can be represented by the following polynomial expression: K = A .* R2 + B * R + C Where A, Band C are constants that depend on the nitrogen flow rate and R is the air-fuel ratio or the steam-fuel used in the reducing step. Depending on the optimization of the flow of nitrogen and the air-fuel or steam-fuel mixture and only if just the oxidation, complexing and reducing steps are considered, the process cycle might be shortened by 45%.

Jan 1, 2003

By Mario H. Castro-Cedeno

"A design for a handheld MEMS chemical detector is proposed. The detector will be used to detect trace amounts of chemicals in air. It can detect drugs, toxic chemicals and/or explosives. The proposed detector will use ion mobility spectrometry (IMS), a technique that is well known for accuracy and has been used in the past in suitcase sized chemical detectors. The separation and detection of the chemicals occurs in the drift channel and the process was modeled using the finite element method and CoventorWare modeling software. A manufacturing process sequence for the drift channel is proposed and was demonstrated.IntroductionThe goal of this effort is to design, mode~ and prototype a MEMS chip that will be the key component in an ion mobility spectrometer (IMS). This technique uses and asymmetric potential to separate the various ion species in a stream of incoming air [1-4]. One advantage of IMS is its ability to separate chemical species from air at atmospheric pressure and temperature. This is a requirement for a simple to use handheld drug or chemical detector. IMS can be used to detect drugs, toxic chemicals and explosives and it is well known for accuracy in detecting very small amounts of chemicals. This chemical detection technique has been used in the past, but not in handheld detectors.One variant of IMS is the high-field asymmetric waveform ion mobility spectrometry or FAIMS [3]. The FAIMS process, shown in Figure l, works as follows: a gas sample is admitted into the instrument where gas molecules are ionized, typically by a weak radioactive isotope source, ultraviolet light source; and more recently through field emission. The ions move along the length of a channel while they are separated in the transverse direction by an asymmetric electrical potential. The potential, in the form of an asymmetric waveform, causes relative motion between the various chemical species. The species that hit the charged top and bottom plates are neutralized and only those ions that move along the center are detectable as charged chemical ions at the end of the channel."

Jan 1, 2004

By Dr. -Ing. Wolfgang Pietsch

Many primary metallurgical wastes are in the sh.-ape of turnings; borings, chips, dusts, and other particuletes. While such. materials can be easily segregated and/or upgraded to yield high quality ?secondary metals with often known composition for easy recirculation into the production? process; their particulate nature results in various problems. Roller presses are used in an ever increasing number for size enlargement and densification of primary particulate metallurgical wastes for secondary metal recycling. The paper will mention the areas of application from A(luminum) to Z(ink), also including Brass; Cast Iron, lead, and Stainless Steel, as well as dusts from all types of melting and ladle furnaces or converters. Typical systems using roller presses for size enlargement. will be discussed.

Jan 1, 1995

Thallium is a very minor element found in lead ores. It&apos;s behaviour during lead smelting has recently become of much greater interest due to the effects it had on the health of waste heat boiler maintenance contractors at a Canadian smelter. In this paper the behaviour of thallium in both traditional and direct lead smelting processes will be examined using computational thermodynamics techniques. Yazawa and his coworkers have made extensive use of computational thermodynamics to examine and illustrate pyrometallurgical processes. It has been shown that thallium behaviour during smelting is strongly influenced by the extent of oxidation of the lead concentrate and by the presence or absence of chlorine in the charge. The condensation behaviour of thallium species in the waste gas handling system was also modelled and it has been confirmed thallium-rich deposits can form at the high temperatures prevailing in waste heat boilers.

Jan 1, 2003

By Naiyi Li, Henry Hu, Alfred Yu

"In the past few years, various squeeze cast aluminum components have been developed and successfully implemented in various vehicles by the automotive industry because of their superior engineering performance. However, fundamental understanding of the formation of air gap during squeeze casting processes is still very limited despite of its significant influence on the extent of heat transfer between the casting and mould. In this paper, a mathematical model has been developed to simulate phenomena of air gap between the casting and mold' during squeeze casting of aluminum alloys. The model considers the effect of process parameters such as applied pressures and mold temperatures on the events of air gap formation. The predication indicates that the occurrence of highly enhanced heat transfer in squeeze casting of aluminum alloys primarily results from the presence of excess applied pressures.IntroductionA number of squeeze cast Al components has been developed and used in mass-produced vehicles in the past few years, such as steering knuckles, Road wheel, Engine Block etc. This is attributed to their superior engineering performance. In squeeze casting, the cooling rate can be increased by applying high pressure during solidification which results in the noted refinement in the micro structure scale leading to better casting properties. However, the excessive pressure increased interfacial heat transfer coefficient is affected during the solidification by air gap formation and die surface condition etc., which is believed to increase thermal resistance at the casting/die interface [l - 4]."

Jan 1, 2004

By A. González

Arsenic is one of the main contaminants present in Chilean copper concentrates and its abatement represents a challenge for the process metallurgy, particularly under the strong environmental requirements in the global community. The possibility to form ferric arsenate directly from a gas phase by means of a heterogeneous reaction between an arsenic gas bearing and iron oxide was studied at laboratory scale. A thermodynamical analysis for the system Fe-As-O-S has been initially made, in order to obtain the stability conditions for the ferric arsenate or other FeAsyO2 type compounds. Experiments were made using an hematite sample suspended in a thermogravimetric device. AS4O6 gas generated from solid AS2O3 that was passed through the iron oxide sample and its instantaneous weight change was recorded directly. A kinetic study for the AS4O6 volatilization was made to control the gas composition. A chemical control between 300 and 600°C with an apparent activation energy of around 14 Kcal/mol As2O3 was determined. The samples after the reactions were chemically and XRD analysed. Arsenates detected corresponds to complex compounds. Results shows a dependence on temperature and oxygen content in the gas phase. The kinetics for iron arsenates formation is slow, reaching an arsenic capture of 6% after 80 minutes of reaction when an oxygen content of 50% is fed continuously at 800°C and 3,56% As in the gas. Experiences made at the same temperature but under higher oxygen content in a closed reactor, allowed arsenic capture close to 60%. For higher temperatures the capture is considerably lower.

Jan 1, 2003

The standard procedure of fire refining consists of sulphur removal via air injected through tuyeres, arsenic slagging via soda-lime flux and oxygen reduction by air or oxygen deficient air or a steam fuel mixtures. The use of porous plugs to stir with an inert gas has been mainly considered as a surface renewing agent that increases the product quality and shorten the refining cycle. In the present study the effect of the bottom stirring by nitrogen gas injection through porous plugs for the treatment of the crude copper in the range of 400-150 ppm sulphur, 3,000-2,000 ppm arsenic and 14,000-7,000 ppm oxygen content was investigated. The combined effect stirring-reducing, by the use of air or a steam fuel mixtures through tuyeres for oxygen removal, follows a kinetics of first order where the constant, K, can be represented by the following polynomial expression: K = A * R2 + B * R + C Where A, Band C are constants that depend on the nitrogen flow rate and R is the air-fuel ratio or the steam-fuel used in the reducing step. Depending on the optimization of the flow of nitrogen and the air-fuel or steam-fuel mixture and only if just the oxidation, complexing and reducing steps are considered, the process cycle might be shortened by 45%.

Jan 1, 2003

By Kazuhiro Asai

Hitachi Refinery of Nippon Mining & Metals Co., Ltd. installed a reverberatory type recycling fumace in 1978 in order to treat the industrial wastes which contain metal elements such as copper, gold and silver. Pyrite and industrial waste materials such as galvanizing sludge, hydroxide slime and dust are smelted. Sulfidized copper, iron and precious metals are transformed into matte and other metallic elements are oxidized into slag This copper matte is transported to Saganoseki smelter and copper and precious metals in the matte are recovered. Recently it is difficult to obtain pyrite economically because of the decrease of pyrite production. Therefore, a new treating process of the liquid waste has been investigated at Hitachi Refinery. In this process, the sulfide or sulfate from the liquid waste are smelted as a source of sulfur.

Jan 1, 1997

By Yuanbo Zhang, Zhixiong You, Guanghui Li, Peidan Wen, Tao Jiang

Sn-bearing iron ore containing small amount of Zn, Pb and As is one of the typical complex polymetallic ores in China. This kind of ore is not extensively utilized due to the complicated relationships between iron and other associated nonferrous metal minerals. Excessive contents of these elements would adversely affect the metallurgical operation as well as the quality of steel products. In this study, reduction behavior of Sn was detailedly investigated using H2 or mixed H2/CO as reductant. The results revealed Sn volatilization was improved in the presence of H2 than individual CO/CO2 atmosphere. Simultaneous volatilization of these elements was realized by roasting under weak H2/CO reducing potential, and metallization reduction was advantageous for further Zn volitilization. A metallic pellet (DRI) with Fe metallization greater than 90%, residual Sn, Zn, Pb and As content of 0.054%, 0.012%, 0.0045% and 0.09% was prepared via a simulated reducing gas of coal gasification.

Jan 1, 2015

By N. Choi

The distribution behavior of selenium and tellurium in nickel sulfide smelting was investigated in the temperature range of 1250-1300 °C under an inert gas atmosphere and various oxygen partial pressures. The distribution coefficients of selenium and tellurium between nickel-copper-iron matte and silica-saturated iron silicate slag were detennined in terms of matte and slag compositions, temperature, and oxygen partial pressure. The effect of slag additives such as CaO, MgO, and Ah03 on the distribution coefficients of those elements was also investigated. It was observed that the distribution coefficients of selenium and tellurium increased with increasing matte grade and temperature. The solubility of selenium and tellurium in the slag decreased with increasing the partial pressure of oxygen within the range investigated in this study. The distribution coefficients of selenium and tellurium increased with the amount of CaO and MgO. Tellurium distribution coefficients also increased by the addition of Ah03. Meanwhile, the addition of Alz03 decreased the distribution coefficients of selenium at high matte grade.

Jan 1, 1996

By P. H. Chang, J. E. Gould

"Solidification structures and austenite decomposition in some spot welded O.05%C - O.3%Mn steels have been studied with the aid of a numerical thermal model. The model is a one dimensional finite difference formulation, and accounts for melting, temperature dependent thermal properties, effective heat transfer in the liquid, and contact resistances. The model was used to predict solidification conditions during resolidification of the nugget. These solidification conditions were correlated with the primary dendrite spacing using available primary dendrite spacings modelling. The model was also used to predict cooling rates in the temperature regime for austenite decomposition. These cooling rates were used to interpret the underlying microstructure.INTRODUCTIONThe metallurgical transformations which occur during the spot welding of low carbon steels have traditionally been characterized only in the most general of fashions. This is most probably due to the similarity of spot welded microstructures to other welded microstructures, and that the mechanical integrity of spot welds has not been a concern. In addition, little information about the particular thermal cycles experienced during spot welding has been available. The introduction of HSLA (microalloyed) sheet steels has, however, raised new concerns about the integrity of spot welds. These steels have on occasion shown irregular weldability, as well as brittleness in the weld nugget on destructive testing l - 4 .In response to these concerns, considerable work has been done attempting to characterize thermal cycles in spot welds 5-12. This has largely taken the form of thermal modelling, with the end purpose generally to estimate the size of the nugget formed. This work uses the thermal model developed at Inland Steel 13 ,14 to try and understand, in a more fundamental way, microstructural evolution in spot welds. Two facets of this microstructural evolution are examined in detail:"

Jan 1, 1986

By Gerald M. Rich

Magma Copper Company, a subsidiary of Newmont Mining Corporation, has initiated many changes in the continuous casting of 5/16 inch diameter copper rod since startup of the San Manuel rod plant in early 1972. With rod production at forty percent over design capacity, many production records have been established including a record cast of 761 tons of salable rod in a twenty-four hour period. The most challenging and rewarding introduction was the continued utilization of an alloyed copper casting wheel in lieu of the conventional steel wheel. With proper cooling and careful control of the mold release agents. as much as 58.000 tons of copper were cast on a single copper wheel. Other advantages are: 1) Fifteen percent increase in available casting time 2) Reject rod from steel inclusions was reduced by nearly one-hundred percent 3) Wheel cost was decreased by ninety-one percent 4) Natural gas consumption dropped approximately fifteen percent 5) Large increase in refractory component life 6) Reduction of manhours/ton. Many other modifications have contributed to excellent rod quality and high operating efficiency. A two-piece launder was replaced with a single castable launder which reduced oxygen pickup and provided better slag removal. Modifications to the bar preparation unit, pickling system, and coiler resulted in considerably higher milling efficiency.

Jan 1, 1976

By Jordan Mayorga, Joseph Kopp, Robert Boehm, Daniel P. Cook

"Solar generated power has long been considered a useful energy source only for low-energy density and non-mission critical use, such as providing electricity for residential applications. The success of Concentrating Solar Power (CSP) facilities, such as the 64 MW Nevada Solar- 1 near Las Vegas, have demonstrated that solar does have application to high energy density industries such as materials and chemical production. This paper will discuss the current operating con_guration of the Solar-1 facility and show how proposed modi_cations, such as addition of thermal storage and use of liquid salts as the working uid, can further improve the e_ciency and energy production of the plant.IntroductionThe United States as a nation is the largest consumer of energy in the world at an estimated 29 trillion kWh per year[1], which is roughly 15% of total global energy consumption[2]. On a per capita basis, the United States also leads most of the world, using an average of 96,000 kWh per person[3]. Roughly 40% of the energy consumed in the United States was produced from petroleum, 23% from coal, 23% from natural gas, 9% from nuclear and the remaining 5% from renewable sources such as solar, geothermal, wind, and hydroelectric[1].Energy demands associated with the industrial-scale production of chemicals and materials is a signicant portion of the United States total energy consumption. Roughly 33% of the energy consumed in the United States is used by the industrial sector, with 22% of this amount used in chemical production, 16% used in petroleum rening, and 14% used in the smelting and rening of metals[1]. Energy costs are also a signicant, if not the most signicant, portion of the total production costs for many materials. For example, roughly 30% of the cost of producing aluminum is the electricity used in the Hall-Heroult process [4], while the cost of energy is roughly 15% of the total cost of producing steel products [5].The primary sources of power for the industrial sector have been coal, petroleum, hydro- electric and nuclear. The use of alternative energy sources, e.g. solar, wind, geothermal, for industrial materials production has been slow in coming because they are intermittent and low-energy density sources, i.e. no solar power at night, no wind power when the air is still, etc. The success of Concentrating Solar Power (CSP) facilities, such as the 64 MW Nevada Solar-1 (NS-1) near Las Vegas, have demonstrated that solar can have application to high energy density industries such as materials and chemical production.This paper will discuss the current conguration of the NS-1 facility, and potential modications to the facility that will increase both its power e_ciency and power density."

Jan 1, 2010

By Yurniko Nakamura

Hydriding properties and crystal structure of a Ti-V- Mn solid solution alloy have been studied by P-C isotherm measurements and neutron and X-ray powder diffraction. The absorption P-C isotherm at 298K shows two plateau regions at 0.01MPa and 1MPa. The X-ray diffraction data have demonstrated that three phases with a BCC, a pseudo-cubic FCC and an FCC structure form subsequently with increase of the hydrogen content. Crystal structure of the latter two phases has been determined by Rietveld refinement of the neutron diffraction data. The FCC phase is the di-hydride of CaF2 type with hydrogen occupation in the T sites. The pseudo-cubic FCC phase is the mono-hydride of NaCl-type with hydrogen occupation in the 0 sites, which has not been reported so far. The lattice constants of the mono-hydride (Ti1.0V1.1Mn0.9)H_2.7 are a&apos;=0.407 nm for two axes and c&apos;=0.390 nm for the third axis. The a&apos;axis is shorter by 4% than the c&apos;axis. This pseudo-cubic FCC lattice is formed by contraction of 5% of the a axis and expansion of about 30% of the c axis from the original BCC lattice.

Jan 1, 2002