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By D. Pradhan, R. G. Reddy

"Electrorefining of aluminum scrap was investigated from AlCl3 –1-Ethyl-3-methyl-imidazolium chloride (EMIC) (Molar ratio 1.65) chloroaluminate electrolyte using copper cathodes at temperature of 90±3°C and cell voltage of 1.5 V. The deposits were characterized using scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD). The study was focused to determine the effect of electrode surface modification as well as deposition time on dendritic depositions of aluminum. Their effect on current density was investigated also. It was shown that the surface modification of electrodes reduced the dendritic depositions of aluminum. Pure aluminum (>99%) was deposited for all experiments with the current efficiency of 94-97%. The use of ionic liquids not only reduced the energy consumption but also minimized pollutant emissions (CO, CO2 etc.) compared to the commercial high temperature aluminum production.1. IntroductionAluminum electrorefining/recycling from aluminum scrap using ionic liquid electrolyte is an attractive process today because of the unique chemical and physical properties such as wide temperature range for the liquid phase, high thermal stability, negligible vapor pressure, low melting point and wide electrochemical window. But in conventional practice, melting of aluminum scrap and high temperature molten salt electrolysis makes this process more expensive and less energy intensive (average 13 kWh/ kilogram of aluminum) [1] . Although recycling scrap aluminum requires only 5% of the energy used to make new aluminum [1-2], but the green house emissions like CO2, CO and HF have to be counted for environmental reason. Approximately, 5.31 kilogram of CO2 emitted per kilogram of aluminum production in most of the US industries."

Jan 1, 2009

By Hiroaki Kawamura, Takeshi Yoshikawa, Kazuki Morita, Yutaka Yanaba

"To develop an alternative metallurgical process for phosphorus removal in the production of solar-grade silicon (SOG-Si), slag treatment of metallurgical-grade silicon (MG-Si) was conducted, followed by acid leaching. Phosphorus-doped silicon alloy or MG-Si containing certain amounts of phosphorus and calcium was reacted at 1723 K and 1773 K with CaO--CaF2 of several compositions. Phosphorus removal from the molten silicon into the slag phase was confirmed by reduction to phosphide ions, P3-, and phosphate ions, P3-. These ions were separately determined using a wet chemical analysis method developed by ourselves. The highest phosphorus distribution ratio obtained was 2. 7 after reaction for 18 h with 17.5 mass% CaO--CaF2 slag. We then conducted acid leaching of the silicon and achieved removal of a large fraction (over 90 % ) of the phosphorus, which was much higher than that obtained by ordinary oxidizing slag treatment.IntroductionIn recent years, the production of solar cells has been increasing rapidly. Because of this, the demand for solar-grade silicon (SOG-Si) has also been growing rapidly. The development of lower-cost mass production processes is therefore needed to provide silicon feedstock. Phosphorus is one of the impurities in metallurgical-grade silicon (MG-Si). Because of its large segregation coefficient (kp = 0.35) [l ], it is difficult to remove phosphorus using a solidification refining process. Vacuum melting is considered to be a promising method for removing phosphorous from MG-Si [2], but the issues of high cost and large energy consumption have still to be resolved.Slag treatment is often used to remove impurity elements by oxidizing reactions during general oxidation refining processes. For example, phosphorus in molten steel is removed into a slag phase as phosphate ions, PO4 3-l-, by the following reaction:"

Jan 1, 2013

By James T. Staley

Quenching and aging are critical processing steps used to produce precipitation hardenable aluminum alloy products. This work describes personal computer programs that employ models to predict certain properties after quenching and aging and graphically display them. One of the programs allows the user to predict the attainable strength and toughness of aluminum alloy products after an arbitrary quench. Another program simulates the changes in strength and electrical conductivity occurring during second-step aging alloy 7050-T7X products as a function of thickness, furnace temperature set point, and furnace characteristics.

Jan 1, 1993

By Jie Ma, Shun-Li Zhao, Jian Zhao, Jie-Yu Zhang

"Microstructural morphology evolution of Ni-45wt.%Mo droplets during rapid solidification process was investigated using an advanced modified 3D cellular automaton-finite element(CAFE) model by CALCOSOFT software. The model was modified by User-defined functions (UDFs) and validated with experimental solidification microstructural morphology of Ni-45wt.%Mo droplets available in the literature. Then, the influences of convection heat transfer coefficient, superheat of the alloy droplets and droplets size were investigated during the rapid solidification process. The predictions show that microstructural morphology is obviously sensitive to convection heat transfer coefficient and droplet size. With the decrease of convection heat transfer coefficient, the grain density decreases. In addition, the decrease of the droplet size could obtain refined microstructure. However, decrease the superheat ofNi-45wt.%Mo droplets has little effect on microstructural morphology.IntroductionFor several decades, much attention has been paid to undercooled alloy droplets of rapid solidification process for which can obtain refined microstructure, decreased microsegregation and extended solubility of alloying elements [1-3]. Extensive prior work shows that solidification of droplets plays an essential role in advanced material properties [ 4]. Consequently, it is very important to investigate the microstructural morphology evolution, especially for dendrite growth during non-equilibrium solidification process, for dendrite growth reflected the kinetics of the crystal growth process."

Jan 1, 2013

By Yin Zhang, Xiaoyu Huang, Mi Wang, Bencheng Du, Youduo He

"Burners are important facilities for blast furnace stoves to raise hot-blast temperature up to 1200°C. Common types of two-ring ceramic burners have very long flames so that part of combustion occurs in the upper part of the chequers and will cause damage to the refractory materials. Using computer simulation to analyze the turbulent diffusion flame in the combustion chamber, some good results were obtained. A new type of ceramic burner will be installed by Anshan Steel Complex in stoves of blast furnace number 4. A pilot experiment was done on the new burner. The experimental data have shown that the mixing condition was improved and the length of flame was shorter with the new type of ceramic burner.IntroductionPulverized-coal injection can give significant operating saving, reducing coke rate in blast furnace(BF) operation. However, during high rates of coal injection, extra heat must be compensated in hearth to maintain certain raceway adiabatic flame temperature. One of the effective methods for heat compensation is to raise hot-blast (HB) temperature up to 1200°C. Nowadays, since the fuel being combusted in stoves is BF gas only, in which the calorific value is down to round 3000 kJ/m3 , to increase the combustion ability and to provide a suitable length of flame in combustion chambers of stoves becomes more important. In other words, designing a good ceramic burner which will affect to HB temperature and stove lifetime is drawing more attention."

Jan 1, 1999

By Gökhan Demirci, Ishak Karakaya

"Energy consumption in electrolytic magnesium cells is well above the theoretical values. However, the mechanism of the back reaction, the main cause of the current losses, has not been fully understood yet. Magnesium dissolution into the melt is generally regarded as the limiting step for the back reaction. Accordingly, present cell designs are made with priority given to fast magnesium removal from the cell. However, experimental data and modeling results in this study indicate that the limiting step for the back reaction between magnesium and chlorine is the chlorine dissolution into the electrolyte when physical contact between electrolysis products was eliminated. Effects of chlorine bubbles on the current efficiency and the cell potential were investigated. Results show that the extent of back reaction is proportional to the chlorine surface area in contact with the electrolyte per unit time, and the cell potential increases with the amount of chlorine bubbles inside the electrolyte.1. IntroductionMagnesium is less dense than the electrolyte in electrolytic magnesium production. Therefore, both electrode products, magnesium and the chlorine gas, move upwards inside the molten salt electrolyte during electrolysis. The upward motion of electrode products promotes the most important current loss mechanism, the ""back reaction"". Separation of the highly reactive species; liquid magnesium and the chlorine gas in the cell, to prevent their recombination is one of the main concerns in cell designs. The employment of large inter-electrode distance or a separation wall in early cell designs; decreased the extent of recombination, but increased the cell voltage and energy consumption. Recent cell designs, on the other hand, make use of lifting action of chlorine gas [1,2] by utilizing smaller inter electrode distances to separate the magnesium and chlorine gas faster. Although energy consumption was reduced, but more physical interactions between electrode products make electrolytic magnesium cells still highly inefficient when energy consumptions are compared with the theoretical values. Today, the most efficient industrial cells utilizing high purity feed operate at 10.5-11.5 kWh kg-1 Mg [3-5] and it is considerably higher than the theoretically attainable value of about 6.0 kWh kg-1 [6]. This large gap demonstrates the necessity of more research on physics and chemistry of magnesium cell electrolysis."

Jan 1, 2011

By Wayne Bell, Shivanand A. Borkar, Anish Upadhyaya, Matthew D. Andriese, Jiann-Yang Hwang, Zhiwei Peng

"A refractory ore body located in Michigan’s Upper Peninsula contains high concentrations of nickel and copper chiefly occurring in the minerals pyrrhotite, chalcopyrite, and pentlandite. Refractory ore bodies are difficult to treat by conventional mineral processing methods so microwave pre-treatment of the ore is employed to increase metallic-particle/host rock liberation by making use the differential thermal expansion properties of the mineral phases that absorb microwave energy. The Curie temperature measurement of metallic-bearing particles is in agreement with the known value for pyrrhotite occurring at 325°C. A nickel-rich iron sulfide mineral is found to be in occurrence and also appears to be magnetic under BSE imaging. It is shown the ore particles heat rapidly when exposed to microwave radiation for short durations of time mainly due to the high concentration of ferromagnetic mineral phases. Rapid heating causes thermal expansion of constituent mineral phases that produce cracks within ore particles. SEM imaging shows fracture occurring along grain boundaries and throughout host rock matrix. Ball milling experiments show an increased grindability of the ore resulting in a decrease in work index values.IntroductionCrushing and grinding operations consume 50-70% amount of energy used in mineral processing operations [1]. All these processes involve high energy impact of surfaces to develop compressive stresses that produce cracks to initiate breakage of particles. Microwave pre-treatment of certain types of ore might provide an energy savings to these type grinding processes by taking advantage of the tensional forces produced by selectively heating microwave absorbing type mineral phases. The heating of ore particles produces cracking by thermal expansion of the constituent mineral phases. Conventional heating has been investigated and shown to positively aid in grinding processes but determined energy inefficient to be used commercially."

Jan 1, 2011

By Paul O. Malan

"The Tusc gold deposit is located along the Carlin Trend approximately 13 kilometers north of Carlin, Nevada and 2.5 kilometers northwest of the Gold Quarry mine. Tusc is one of several structurally controlled oxide gold deposits located along the Good Hope fault within the Maggie Creek subdistrict. Mining commenced in 1994 with an oxide reserve of780,000 troy ounces of gold at an average grade of 1.34 g/t Au. The Good Hope fault forms the southwestern edge of the Schroeder Mountain uplift (also known as the Carlin Window) and juxtaposes carbonate rocks of the Siluro-Devonian Roberts Mountains Formation against siliceous mudstone, siltstone, and silty limestone of the Devonian Rodeo Creek unit. Submicroscopic gold mineralization is disseminated in the Good Hope fault system and in fractured hanging wall carbonate rocks. Wallrock alteration includes silicification, deca!cification, sericitization, and late alunite replacement and veins. All Tusc ore is transported 2.5 kilometers to Gold Quarry for processing. Leach-grade ore (0.2 - 1.7 g/t gold) is placed on the oxide leach pads, and mill-grade ore(> 1.7 g/t gold) is processed through the CIL oxide mill. IntroductionThe Tusc gold deposit is located in Eureka County, Nevada, U.S. A, approximately 13 kilometers north of the town of Carlin and 2.5 kilometers northwest of the Gold Quarry mine (Fig. 1 ). Tusc is one of several open-pit, oxide, gold deposits within the Maggie Creek subdistrict of the Carlin Trend. Tusc is a structurally controlled gold deposit located along the Good Hope fault. Submicroscopic gold mineralization is disseminated in the brecciated and silicified Good Hope fault zone and along intersecting northeast and northwest striking structures."

Jan 1, 1997

By Kyle S. Brinkman, Kenneth L. Reifsnider, Fazle Rabbi

"Mixed ionic and electronic conducting (MIEC) ceramic membranes are HeteroFoaM's which play an essential role in a number of energy conversion related systems including the solid oxide fuel cell (SOFC), oxygen separation and permeation membranes, partial oxidization membrane reactors for natural gas processing, and high temperature electrolysis cells. Dual phase oxygen membranes consisting of an ionic conducting phase Ceo.sGdo.z02 (CGO) and an electronic conductive phase C0Fe204 (CFO) were fabricated and characterized by structural (XRD), microstructural (SEM-EDS) and broadband dielectric measurement techniques. In-situ measurements of the dielectric properties of working oxygen separation membranes are presented which indicate that the material's dielectric behavior can be an indicator for MIECperformance.IntroductionCeramic membranes which transport oxygen ions play an essential role in a number of energy conversion related systems including the solid oxide fuel cell (SOFC) [l ], oxygen separation and permeation membranes in the commercial and nuclear arena [2, 3], partial oxidization membrane reactors for natural gas processing [4], and high temperature electrolysis cells [5]. For the electrolyte functions, the membranes must transport oxygen ions only. On the other hand, permeation membranes, typically used in combustion devices to support oxy-fuel combustion or for partial oxidation reactions involving the production of synthesis gases, require mixed oxygen ion and electronic conduction (MIEC). Traditionally the tailoring of the ratio of ionic conductivity to the materials electronic conductivity, measured as the transference number, has been accomplished by the introduction of aliovalent doping elements creating point defects in the material facilitating the diffusion of charged species. However, several decades of research have not yet produced single phase materials which possess the concomitant ionic and electronic conductivity required for use in membrane separation applications. It is clear that novel ""dual phase"" heterogeneous materials will be required and that the surface reactions of these materials will be of particular importance as the industry moves toward thin films membranes [6]."

Jan 1, 2013

By Ryokichi Shimpo, Akio Fuwa

"The process-measurements of copper smelters in Japan were investigated for the summary of the latest technique and for the fundamental study of process control. The smelters investigated are those employing flash smelting furnace and P.S. converter, one reverberatory furnace and P.S. converter, and one continuous smelting converting furnace (M.I. process). Respective process is then considered, consisted of several reactors of different functions. The measurement methods were summarized in each reactor, including the measurement points. The methods of chemical analyses of the samples in each reactor were also investigated.IntroductionAn investigation on the process measurements, chemical analyses, and system control in copper smelters in Japan were carried out for understanding and summarizing the technique of the pyrometallurgical copper smelting operations. The typical seven processes in six copper smelters were investigated in the period from 1985 to 1987. The smelters investigated were Touyo Smelter of Sumitomo Metal Mining Co., Ltd., Kosaka Smelter of Dowa Mining Co., Ltd., Saganoseki Smelter of Nippon Mining Co., Ltd., Tamano Smelter of Hibi Kyodo Smelting Co., Ltd., Ashio Smelter of Furukawa Co., Ltd. and Naoshima Smelter of Mitsubishi Metal Co., Ltd. They include five flash smelting furnace and P.S. converter systems, one Mitsubishi continuous smelting and converting process (M.I. process), and one reverberatory furnace and P.S. converter system.The investigation was performed by making inquiries about the measurements, chemical analyses, system control, and their future prospects to the engineers in each smelter and by summarizing up in each item. The system control and future prospects were summarized in another paper titled ""Process Control Scheme of Copper Smelting Processes in Japan and Future View."

Jan 1, 1989

By Wenbo Luo, Jilai Xue, Tiepeng Li, Jun Zhu

Sodium silicate solutions for producing silica have been ultrasound treated to enhance the precipitation process in laboratory scale. Higher precipitation rate was found with ultrasound treated solutions than those without ultrasound. The obtained SiO2 powder products were characterized using XRD, SEM, BET and laser particle size analyzer. The particle size distribution and the specific surface area of the powder products varied with the power input level and the processing time of the ultrasonic treatment. The results indicate that the efficiency of the precipitation process can be improved optimally when the ultrasound is conducted into the solutions before the nucleation stage.

Jan 1, 2015

By Bing Song, Fei Xi, Xuewei Lv, Kai Zhang

The electric arc furnace process is a common method to produce high TiO2 slag from ilmenite. The pre-reduction process was proposed in recent years in order to reduce electricity consumption. In order to enhance the pre-reduction degree, high energy ball milling was proposed to improve the specific surface area of the ilmenite prior to reduction. In this study, the carbothermic reduction behavior of milled ilmenite concentrate was investigated. It was found that the ball milling method can result in a higher reduction rate and improved metallization of iron. The metallization of iron increased with increasing the time of ball milling. The metallization of iron with milling reached 89.49% when the time of ball milling was 70 min., while the FeO content decreased with 70 min. of milling from 11.84% to 4.76%.

Jan 1, 2014

By Grant Wallace, Rod James, Larry Twidwell, Ed Rosenberg, Courtney Young, Sean Dudley, Hsing-Hsin Huang, William Gleason, Jerome Downey

The use of applied chemistry in the production and optimization of leach solutions from Rare Earth Element (REE) ores and concentrates is being investigated. Ore and concentrate samples were characterized using scanning electron microscopy/mineral liberation analysis (SEM/MLA), X-ray diffraction (XRD), and Atomic emission inductively-coupled plasma spectroscopy (ICPAES). Multiple leach tests were performed to analyze the effects of temperature, residence time, and reagent concentration on the leaching of REEs. Analysis of leach solutions was carried out using ICP-AES. Modeling and statistical analysis of extraction behavior was carried out using DesignExpert 9. Modeling data for cerium extraction indicates that extraction is greatly influenced by temperature and reagent concentration, while leaching time plays a much less important role. Experimental design techniques are being utilized to optimize REE recovery. Results, conclusions, and directions for future studies will also be discussed.

Jan 1, 2015

By Ann M. Hagni

Flash reduction of zinc oxides is an alternative, environmentally safe method to leaching and electrowinning for zinc recovery. Zinc and lead are volatilized in a flash reactor, a non-hazardous residue is generated, and the fuel source is inexpensive coal in the flash reduction process. Results from experimental laboratory tests yielded low zinc recovery for this process. Mineralogical and textural characterization of the residues from the flash reduction tests for different feed materials and temperatures were conducted to determine the cause for the low zinc recovery. Reflected light microscopy, cathodoluminescence microscopy, scanning electron microscopy-energy dispersive spectroscopy, and X-ray diffraction were utilized in this applied mineralogical research. The original zinc calcine is composed primarily of fine-grained, iron-bearing zincite particles, 25-40 um in diameter, in a porous texture. Pellets processed at 1150°C were found to produce reaction rims of franklinite-magnetite-jacobsite solid solution that are 125-200 um thick and surround cores of unreacted iron-bearing zincite in a Zn-Fe-Si-Ca glass matrix. The reaction rims have subsequently oxidized to form an outer 10 ~m thick rim of hematite. Slags from calcines processed at 1275°C are primarily triangular particles with porous centers, cenospheres, and spheres of iron-bearing zincite, in addition to rectangular particles composed of non-porous franklinite-magnetite solid solution cores with iron-bearing zincite rims. Slag particles from calcine processed at 1200°C are predominantly 100-250 ~m triangular-shaped, spheres, and cenospheres containing fine-grained franklinite and franklinite-magnetite solid solution in an iron-bearing zincite matrix. Slag from calcine processed at 1300°C are also predominantly 1 00-250 um triangular-shaped, spheres, and cenospheres but contain coarser-grained iron-bearing zincite. The zincite in the penets and the slags typically contain 10-20% iron. Based upon these mineralogical observations, it is concluded that the significant amounts of iron in the zincite prevent volatilization of the zinc in the flash reduction process.

Jan 1, 1995

By K. Pagalthivarthi, P. V. Desai

"During solidification of alloys, many inter-related physical processes, such as melt convection, mass diffusion, heat transport, macrosegregation and melt-undercooling occur. Several research workers have studied one or more of these effects separately. To answer important questions on solidification behavior, an overall approach interrelating the processes is necessaryAs a first step toward accomplishing the overall modeling, the freezing of a binary liquid metal is examined. The various stages during freezing of the alloy are critically described to build a continuum model for the entire process. Diffusive mixture theory is used to write the conservation equations for the liquid and the mushy zones. The concept of local thermodynamic equilibrium in the presence of curvature effects is used to restrict the number of degrees of freedom within the mushy zone. Constitutive equations relating flux quantities and affinities, the governing differential equations and boundary conditions are discussed briefly for the freezing process.IntroductionA solidification study encompasses such facets as solifidication time, microstructure, macrosegregation of the solute, shrinkage effects and soundness of the casting. Influence of one or more of the coupled heat and mass transfer phenomena such as local solute redistribution, thermosolutal convection, melt undercooling at dendrite tips and heat dissipation to the ambient have all been previously examined [1-3J. Several studies have examined the individual facets of alloy solidification as isolated processses. In fact, the transport processes occur simultaneously and a comprehensive model should include their inter-relationships. In particular, some of the existing studies of the mushy zone [4-6J do not emphasize thermodynamic completeness. This work represents an attempt to develop a thermodynamically consistent model of the entire solidification process on physical grounds."

Jan 1, 1986

By Yuanyuan Wang, Hong Li, Xueting Liu, Hao Bai, Kang Zhou

"Phase change materials are widely used in efficient utilization of energy and new energy technology. Especially, more attention has been paid to composite phase material, which is applied on architectural energy-saving and efficient working fluid. In this paper, stearic acid-silicon dioxide composite material was prepared by sol-gel process from tetraethyl orthosilicate (TEOS) and stearic acid (SA). The material was investigated by Field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR) and Differential scanning calorimeter (DSC). The FE-SEM results show that 3D-grids of silicon dioxide were formed clearly and SA was encapsulated in the silicon dioxide shell. The FT-IR results show that there were no chemical reactions between silicon dioxide and SA, which is the chemical property of the composite material, is stable. The DSC results show that the composite phase change material has favorable heat capacity. This material is expected to be used to make a cooling working fluid.1. IntroductionEnergy thermal storage becomes increasingly prominent issue in recent years, because thermal storage has been used in many aspects, for example, it can be added into building materials to improve heat conditioning. Another potential application of thermal storage materials is that the intermittent waste heat can be collected and recycled effectively by using the thermal storage facility. Thus, energy thermal storage plays a significant role in conserving available energy and improving its utilization [1]. Energy thermal storage includes sensible heat storage and latent heat storage. The latent heat storage has great heat density with a constant temperature during the phase change process [2-5]. Large quantities of latent heat storage will be absorbed and released when phase change takes place. Based on the former researches, some phase change material (PCM), such as fatty acid and paraffin waxes, has been proved to have high latent heat storage capacity and appropriate thermal properties [5-6]. However, using the PCM in energy storage systems directly is restricted, e.g. some properties of organic PCM, like form-stability and thermal conductivity, are not good enough to use. Meanwhile, almost all the inorganic PCMs are corrosive and most materials may cause sub cooling and segregation [7-9].The other problem is that the leakage when the temperature reaches the phase change point. Therefore, encapsulated composite phase change material (CPCM) emerged in order to solve the problem of leaking out, minimize the sub cooling and prevent phase segregation. [10-13] However, the easy flammability of fatty acid also has hindered the development of PCM. Accordingly, it has been found out that silicon compounds are environmentally friendly promising substitutes for halogen-containing flame retardants. Especially, silsesquioxanes are excellent in the flame retardancy. So CPCM can be encapsulated with SiO2 acting supporting material."

Jan 1, 2014

By William A. Hockings

Methods for the measurement of liberation of finely ground iron ores are described. The general method consists of separating a sample of the ground ore into a number of size fractions, followed by measuring the liberation of each fraction. The size separation has been done using electro-formed screens of 20-, 10-and 5-micrometer apertures, and also by air elutriation. Liberation (i.e., the distribution of compositions of individual particles) has been measured by optical microscopy. A computer pro-gram was used to adjust the raw count data so that it agrees with the chemical analyses of the size fractions. Various ways of presenting the results are given, and Some applications of the results to flotation processing are discussed.

Jan 1, 1981

By Bo Zhou

During secondary aluminum recovery, complex aluminum scraps are melted and refined often in a rotary melting furnace and the aluminum metal has to pass through a molten salt layer and melt down in a bottom aluminum bath. Previous experimental study and industrial observations have indicated that salt shell formation and re-melting on the metal solids in the early stage plays a critical role in the overall melting process of the scrap. In the present paper, mathematical models are developed to simulate the process of salt shell formation and its re-melting, as well as aluminum melting in the molten melt. Influence of the salt layer properties, the residence time of the metal particles in the salt layer, the particle size, the temperature of bulk melt were investigated. Reasonable agreement with the measurement data was reached. The developed melting model will be used to construct a population balance model of the scrap melting behavior for a rotary melting furnace, taking into account the distributed characteristics of the scrap. Finally, an overall process model based on Computational Fluid Dynamics (CFD) for the rotary furnace will be constructed, coupling with the population balance model for the scrap melting.

Jan 1, 2003

By James L. Whitlock

Biological treatment of mining and industrial effluents reached full scale commercialization around 1980. These proven, low cost, technologies have been limited in application due to a number of factors, including extended periods of time and cost required for pilot testing as compared to chemical treatment technologies, lack of biological expertise in metallurgical personnel, longer treatment periods in some cases, and performance failures based on improper application. Renewed interest in biological treatment technologies is being driven by permits with lower effluent concentration criteria, permits with bioassay evaluation, the need to remove thiocyanate, nitrates, sulfates and? other parameters. Chemical treatment processes, in general, have not been able to meet these present requirements, or require elaborate? combinations of processes, in terms of effluent quality and treatment economics. This paper addresses biologieal treatment of mining and industrial waste waters and selected recent advances in these technologies. The future looks very bright for application of these low capital and operating cost technologies,

Jan 1, 1998

By Charles I. Richman

Aquispirillum magnetotacticum (AM) is gram-negative hetrotrophic bacteria that belongs to a class ,of magnetotactic bacteria that have an ecological niche in marine marches and fresh water swamp sediments. Thiobacillus Ferrooxidans (TF) is a Gram-negative, acidophillic chemoliths that may have similar chemical conditions within the cytoplasmic membrane as Aquaspirillum M. to support growth of Magnetosomes. Magnetosomes are cellular bodies that accumulate under slightly aerobic conditions. Magnetotactic motion occurs in an external magnetic field and depends on the medium viscosity. The Atomic Force Microscope equipped with a magnetic tip shows the presence of Magnetosomes in these bacteria strains. The size, shape of magnetosomes in AM and TF strains are characterized.

Jan 1, 1998