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By Philip L. Sibrell

A new process utilizing pulsed fluidized limestone beds was tested for the remediation of acid mine drainage at the Friendship Hill National Historic Site, in southwestern Pennsylvania. A 230 liter-per-minute treatment system was constructed and operated over a fourteen-month period from June 2000 through September 2001. Over this period of time, 50,000 metric tons of limestone were used to treat 50 million liters of water. The influent water pH was 2.5 and acidity was 1000 mg/L as CaCO3. Despite the high potential for armoring at the site, effluent pH during normal plant operation ranged from 5.7 to 7.8 and averaged 6.8. As a result of the high influent acidity, sufficient CO2 was generated and recycled to provide a net alkaline discharge with about 50 mg/L as CaCO3 alkalinity. Additions of commercial CO2 increased effluent alkalinity to as high as 300 mg/L, and could be a useful process management tool for transient high flows or acidities. Metal removal rates were 95% for aluminum (60 mg/L in influent), 50 to 90% for iron (Fe), depending on the ratio of ferrous to ferric iron, which varied seasonally (200 mg/L in influent), and <10% of manganese (Mn) (10 mg/L in influent). Ferrous iron and Mn removal was incomplete because of the high pH required for precipitation of these species. Iron removal could be improved by increased aeration following neutralization, and Mn removal could be effected by a post treatment passive settling/oxidation pond. Metal hydroxide sludges were settled in settling tanks, and then hauled from the site for aesthetic purposes. Over 450 metric tons of sludge were removed from the water over the life of the project. The dried sludge was tested by the Toxicity Characteristics Leaching Protocol (TCLP) and was found to be non-hazardous. Treatment costs were $43,000 per year and $1.08 per m3, but could be decreased to $22,000 and $0.51 per m3 by decreasing labor use and by on-site sludge handling. These results confirm the utility of the new process in treatment of acid impaired waters that were previously not amenable to low cost limestone treatment.

Jan 1, 2003

By Marcel Sturzenegger

Though the extraction of copper is well established, generation of sulfur dioxide (S02) is still a troublesome issue. Conventional processes are further challenged by the increasing amount of impurities in the concentrates. Direct decomposition of the metal sulfides into the metal(s) and elemental sulfur under concentrated solar radiation offers a promising path to solve both problems. Thermogravimetric measurements under inert atmospheres have shown that synthetic chalcocite or chalcopyrite yield copper at temperatures as low as 1773 K. Even though optimum reaction temperatures might be somewhat higher, such temperatures are straightforwardly accessible in solar chemical reactors. The absence of oxygen will reduce the extent of slag forming reactions and thereby alter the evaporation characteristics of volatile impurities such as arsenic or antimony. Chemical equilibrium calculations for a chalcopyrite-enargite feed, e.g., have shown that under inert atmospheres arsenic compounds are completely evaporated at temperatures above 1000 K and an effective separation of arsenic from the matte is expected. An important step towards a solar production of copper is the design and testing of prototype solar chemical reactors for this reaction. Numerical modeling is a key tool supporting a rational design but it requires data of the high-temperature properties that prevail in these processes. Development of techniques for determining the essential quantities such as decomposition rates or radiative properties at temperatures up to 2000 K is therefore a main activity in our laboratory in order to control and optimize the process. Though developed in the frame of high-temperature solar technology, the experimental techniques are also suited to advance the understanding of conventional high-temperature processes. Keywords: Solar technology, Sulfur dioxide, Solar Radiation, Thermogravimetry, Chalcocite, Chalcopyrite, Numerical modeling.

Jan 1, 2003

At its Copper Cliff Smelter, Inco Limited processes a bulk copper-nickel concentrate in two Inco oxygen flash furnaces, The furnace matte is converted to low iron matte for further processing, and the molten converter slag is recycled to the flash furnaces. The flash furnace slag is discarded. Natural gas or coke supplies a minor proportion of the process heat requirements, thus limiting the flash furnace matte grade to the target 45% CuNiCo. Coke addition to the furnace offers a potential means of establishing a reducing barrier on the surface of the molten bath. Such a practice would be conducive to producing sulfur deficient (partially metallized) matte. At the same iron content, the iron activity of sulfur deficient matte is higher than that of regular matte. A supernatant coke barrier could, therefore, be expected to lead to higher nickel and cobalt recoveries, reduction or even elimination of magnetite furnace bottom build-up and increased sulfur elimination as S02 in the flash furnace. Preliminary experiments were conducted in a miniplant flash furnace to investigate the effect on process metallurgy of the suggested modified scheme. This paper presents the experimental results and discusses key aspects of the possible operation of the Inco flash furnace with a coke barrier separating the freeboard from the molten bath.

Jan 1, 2003

By Ko-ichiro Ohno

It is recently recognized that the iron reduction and melting as well as the slag separation of a composite of granular iron ore and coal are completed in a very short period of about IO minutes when the composite is rapidly heated up to approximately 1673K. These phenomena are expected to be applied to a new iron-making process. The mechanism of iron ore reduction and iron-slag separation during rapid heating has not yet been revealed and the fundamental research has just started. Carburization of the reduced iron is regarded as one of the most important steps in this process. In the present work, the composite was prepared from four kinds of coal or graphite as a carbon source and electrolytic iron powder as a completely reduced iron ore. The temperature at which the liquid formation and iron carburization occurred was monitored. Direct observation of smelting reduction behavior was made by a confocal laser-scanning microscope combined with the infrared image-heating furnace to clarify the effect of molten ash on iron carburization. It was found that the meltdown temperature of composite became lower as the melting temperature of coal ash decreased. From the observed result, it was presumed that the liquid slag would act as an important media for the carbon transfer from coal to iron. The carburization mechanism during the smelting reduction was estimated as follows. When slag containing iron oxide melted down and contacted carbon, iron oxide in the slag was reduced and the formation of the metallic iron particle as well as the its carburization occurred simultaneously at the slag-carbon interface. Carburized iron particle was carried from slag- carbon to slag-iron interfaces due to the slag convection flow caused by the difference of the interfacial tension between the carbon-slag and iron-slag interfaces. Carburization of reduced iron could proceed with a repeat of the above-mentioned process.

Jan 1, 2003

By Hiroyuki Matsuura

The effects of P20S or Na20 addition on the reaction rate of CO2 dissociation on the surface of FexO-base molten oxides was investigated at 1773K by isotope exchange methodl-6_ The rate constant decreased with increasing P20S content of molten oxides and the residual rate constant was observed at high P20S content On the other hand, the rate constant increased with increasing Na2O content for FexO-SiO2 melts. The rate constant was evaluated by the composition of oxides and the rate controlling step of CO2 dissociation was discussed.

Jan 1, 2003

By Hiroyuki Matsuura

The effects of P2OS or Na2O addition on the reaction rate of CO2 dissociation on the surface of FexO-base molten oxides was investigated at I 773K by isotope exchange method 1-6. The rate constant decreased with increasing P2Os content of molten oxides and the residual rate constant was observed at high P2OS content. On the other hand, the rate constant increased with increasing Na20 content for FexO-SiO2 melts, The rate constant was evaluated by the composition of oxides and the rate controlling step of CO2 dissociation was discussed.

Jan 1, 2003

By Carl A. Kuehn

At Carlin, Nevada, non-indigenous hydrocarbons were introduced as a bitumen phase which was mobilized due to burial under the Roberts Mountains allochthon. similarly, some indigenous organic matter was locally mobilized. Fluid inclusion and paragenetic data of veinlets formed during this hydrocarbon stage, combined with quantitative modelling or organic maturation, indicate that host rocks had evolved past dry gas conditions of around 1550 and l.l+0.2 Kb in the presence of CH4-saturated, highly saline brine by no later than early to middle Cretaceous time. All hydrocarbons present would have been rendered immobile under these catagenic conditions. Crosscutting relationships at several scales suggest that hydrocarbon mobility may have ceased prior to the intrusion of a series of dikes in the mine which have subsequently been altered and mineralized. Apart from subsequent oxidation, the current distribution and high maturity of carbon-rich zones were established prior to gold introduction. No Evidence has been found supporting proposed hydrocarbon "remobilization" during or after gold mineralization and alteration. The high density of the CH4-bearing fluid requires formation at high pressures (near 1 Kb) and precludes their formation as a result of the "cracking-off" of CH4 from organic matter during a thermal event associated with a shallow hydrothermal system. The density and composition of the fluid inclusions restricted to the early hydrocarbon-stages of the Carlin paragenesis are not unique to the sediment-hosted gold deposit environment of north-central Nevada. Similar inclusions are found in authigenic quartz crystals from Paleozoic carbonaceous shales in central Pennsylvania which have experienced normal metagenesis of indigenous organic matter due to deep burial.

Jan 1, 1987

By Xiao Long, Ting Wu, Lilong Zhu, Qian Wang, Shengping He

"During the continuous casting of peritectic steel slabs, mould fluxes with high crystallization capacity are usually chosen for improving slab surface quality. However, the lubrication condition of casting shell also could be deteriorated. Since precipitation of crystals within liquid slag film can change the composition and property of liquid slag over solid-liquid slag film interface region, its impacts on continuous casting process also are not clear. In order to clear this phenomenon, an experiment method was put forward, and mould fluxes for peritectic steel slabs continuous casting were selected and examined. The results reveal that after crystals have been separated, the crystallization capacity of leftover liquid slag increased with different levels, which could deteriorate the lubrication condition of casting shell and cause a series of problems. Thereby, mould fluxes with high crystallization capacity at beginning for heat transfer control and then weaker after crystallization should be considered in the future.IntroductionIn the continuous casting of peritectic steel slabs, contradiction between heat transfer control and slab shell lubrication by mould fluxes has been treated as a key problem for maintaining a smooth manufacturing process [ 1]. Strong and uneven horizontal heat flux over the meniscus region will cause uneven solidification of casting shell, especially for peritectic steel slab with enormous volume change caused by phase transition. All of those could cause surface defects like longitudinal crack [2-4]."

Jan 1, 2013

By Katsuya Kase, Kaname Takeya, Keaji Ohmori, Yoshiyuki Asakawa

"The reduction-diffusion process (the R-D process) using Ca as a reducing agent has been practiced in industry in the production of the SmCos type, the Nd-Fe-B type and the 1b-Fe-Co type magnetic materials. The advantages of the R-D process are the generally high yield of rare earth metals and the single-stage conversion of a mixture of oxides and metal powders into a product of rare earth alloy powders. On the other hand, one of its disadvantages is the slightly high contents of oxygen and calcium. This disadvantage is remarkable in the Nd-Fe-B type. Singe-phase Nd2Fe14B alloy powders with low content of 0 and Ca, is obtained by choosing appropriate raw materials and performing the R-D process in a controlled way. These alloy powders are very suitable for the production of Nd-Fe-B sintered magnets and expected higher magnetic properties by adopting advanced magnet production method.IntroductionThe hard magnetic rare earth transition metal intermetallics, especially, have attained considerable technical importance. Examples are the alloys based on the intermetallics SmCo5[1], SmC017[2], NchFet4B[3], or the recently developed alloy SnuFe11Nx[4]. The reduction-diffusion process using Ca as a reducing agent has been well known as an economical method of producing rare earth based magnet materials[5]. The reduction-diffusion process has been practiced in industry in the production of the SmCos type, the Nd-Fe-B type and the 1b-Fe-Co type magnetic materials. The advantages of the reduction-diffusion process are the generally high yield of rare earth metals, the single-stage conversion of a mixture of oxides and metal powders into a product of rare earth alloy powders, the elimination of the crushing process of the alloy ingot, the inessentiality to special equipment, etc. On the other hand, one of its disadvantages is the slightly high content of oxygen and calcium. This disadvantage is remarkable in the Nd-Fe-B type. An outline of basic studies of the reduction-diffusion process was reviewed from the particular viewpoint of the production of magnet materials by Ogawa [6]."

Jan 1, 1998

By M. Kawakami

In order to make titanium ingot directly from molten slag, the metal pool was tried to form and used as the cathode. The electro-slag remelting (ESR) unit was used for the purpose. The unit is composed of water-cooled copper mold and the DC power source of 2000 A and 100V. The graphite electrode was used for anode and the base plate was used for cathode. The commercial and re-melted slag of CaO-CaF2 was melted in the mold with the addition of TiO2. The following reactions are expected to occur. Ti4+ + 4e = Ti at cathode 2O2- + 2C = 2CO + 4e at anode During the process, large amount of molten slag splashed out from the mold, showing the CO evolution at anode. The metal deposit was obtained but in the form of block and piled up on the base plate. The metal pool was not obtained perfectly because of shortage of heat supply. The cathodic current efficiency was 60 % at maximum. The metal deposit contained much impurity. In order to reduce the impurity and increase the current efficiency, the effect of electrode distance was examined. The electro-slag re-melting of titanium was tried in order to examine the condition to make metal pool.

Jan 1, 2006

By P. A. Olubambi

The effect of ore mineralogy on the bioleaching of metals from complex sulphides was studied by investigating the bioleaching of zinc and copper from a bulk complex sulphide ore from Ishiagu, Nigeria, using mixed cultures of Thiobacillus ferrooxidans, Thiobacillus thiooxidans and Leptospirillum in mechanically stirred reactors at varying particle sizes. Mineral phases within the varied particle sizes of -53, 53, 75 and 106µm were identified using X-Ray Diffraction (XRD), while the elemental distribution within the varied particles sizes was determined by X-Ray Fluorescence (XRF) and Optical Emission Spectrometry using Inductively Coupled Plasma- Optical Emission Spectrometer (ICP-OES). Bulk ore and the leached residues were examined by X-Ray Diffraction. The highest bioleaching recoveries were obtained at particle size of 75µm, while particle size of 106µm gave the least recoveries. Lower recoveries at particle sizes of 53 and -53µm were as a result of their higher silica and siderite content which affects pH, iron mobility and oxidation.

Jan 1, 2006

By Huang Chao

The thermodynamics analysis on reducing-matting smelting of sulfide ore of lead, antimony and bismuth which use ferric oxide as sulfur fixed agent is first analyzed. Due to the analysis of reaction mechanism, ferric oxide is first reduced to ferrous oxide, then ferrous oxide produce reducing-matting reaction with sulfide ore and reducing agent as reaction equation: MeS+FeO+CO=Me+FeS+CO2. The reaction thermodynamic calculation shows that the reducing-matting reactions of lead sulfide, antimony sulfide, Jamesonite, and bismuth sulfide are feasible, but is infeasible for zinc sulfide. These conclusion provide a feasible method for solve the pollution which produced in the smelting of sulfide ore of lead, antimony and bismuth.

Jan 1, 2006

By V. Bhagavathy

This paper describes a method for the determination of traces of rare earths using energy dispersive x-ray fluorescence spectrometry (EDXRF) after preconcentration of their oxine complexes onto activated carbon. Various parameters that influence adsorptive preconcentration of rare earths onto activated carbon viz. pH, amounts of activated carbon and oxine, time of stirring and aqueous phase volume were systematically studied. A numerical method based on simple least square procedure using fifth order polynomial with 25 consecutive values was developed for smoothing and differentiation of EDXRF data which was previously digitized and averaged. First order derivative EDXRF in conjunction with adsorptive preconcentration on activated carbon enables to determine as low as 10 ppb of each of individual rare earth elements.

Jan 1, 1989

By Christian Ludwig, Virginie Silberstein, Rizlan Bernier-Latmani, Simona Regenspurg

"Residues from waste incineration (bottom ashes) form large amounts of heavy metal-rich waste. Theoretically, heating and the addition of chloride to the ashes could remove these metals by formation of volatile metal chlorides. The remaining heavy metal-poor ashes could be used, for example, as cement additives. In the proposed process of our study we used bypass dust from the cement industry as chloride additives to the bottom ashes. We aim to determine experimentally the optimal conditions to remove heavy metals from ashes and to simulate this process by thermo- chemical modeling. In our experiment we investigate heavy metal flows by heating of differently composed mixtures of bottoms ash and bypass dust in dependence of different furnace temperatures (500-1200 °C). Furthermore, we investigate the reactivity (leaching characteristic) of the resulting product in order to predict if secondary residues can be landfilled in agreement to Swiss regulations for inert materials.IntroductionThe incineration of garbage is generally considered as the most environmentally friendly method for the reduction of municipal solid waste. This is because, compared to traditional storage of waste on landfills, incineration produces less greenhouse gases and destroys toxic organic compounds. The released exothermic energy can be recuperated and the residues from the combustion chamber (bottom ash) are strongly reduced in volume. However, they still form about 600 kt of waste per year in Switzerland, which needs to be landfilled. However, these residues could be potentially used as construction materials after mechanically recovering ferrous and non-ferrous metals. However, the resulting ashes (discharged dry or wet) still contain increased amount of heavy metals (exceeding state regulation) requiring them to be finally deposed on a hazardous waste site. A thermal treatment of these ashes could enable both, to separate and recuperate the remaining heavy metals and an inorganic heavy-metal poor material. The evaporation of metals depends on temperature and can be lowered by addition of chlorides, which would lower the boiling point of most metals by formation of metal chlorides (table 1). 745"

Jan 1, 2008

By Clyde S. Brooks

This paper undertakes to assess what opportunities exist for the economical recovery of non-ferrous metals from spent catalysts. The most promising recovery appears to lie with metals such as Co, Mo, Ni, W, heterogeneous catalysts used on a large scale in petroleum processing. Nickel is a metal with diverse applications on a large scale notably in hydrocarbon steam reforming and in vegetable oil hydrogenation. In addition, several of the precious metals, notably Pt, Pd, and Rh, find extensive use in fossil fuel processing and in automotive and power plant flue gas control. The hydrometallurgical and pyrometallurgical alternatives for processing are identified and discussed, especially with citations to illustrate reduction to commercial practice. Promising directions for adaptation of appropriate, economic separation technologies for recovery of non-ferrous catalytic metals generated in significant amounts for the secondary metal markets are identified. Recycling

Jan 1, 2000

By Dale T. Peters

In the United States, the United Kingdom and numerous other countries, copper has long been the plumbing material of choice. This has been the case since the late 1920s in the United States and since World War II in the United Kingdom. However, in recent years the plumbing tube market has caught the eye of the chemical industry, and several plastic resins have been introduced to the marketplace as substitutes for copper in household plumbing systems. One of these, polybutylene tube, had so many failures in the United States that a class action law suit was filed, and the manufactures of this product were forced to create a trust fund of nearly one billion dollars to repair damages caused by their product. Chlorinated polyvinylchloride (CPVC), in rigid pipe form, on the other hand, has been mechanically acceptable albeit its recent introduction precludes the test of time enjoyed by copper tube in this application. This paper reviews the State of California&apos;s portrayal of copper&apos;s environmental effects and will be largely based on the data and information assembled by the Copper Development Association Inc. in its presentation to the State of California in August, 1998 in response to the State&apos;s Draft Environmental Impact Report for Chlorinated Polyvinyl Chloride (CVPC) Pipe for Use for Potable Water Piping in Residential Buildings. The paper is intended for use as a model for the use of other copper organizations and individuals in responding to similar situations.

Jan 1, 1999

By Zenon R. Llanos

"The disposal of spent hydroprocessing (HDP) catalysts in the petroleum refining industry has been a concern in the past due to their classification as listed hazardous wastes. However, because these catalysts have higher metal concentrations than regular ores, and the recent surge in prices for molybdenum, vanadium, nickel and cobalt what used to be considered as a liability for generators is now viewed as a valuable renewable source of strategic metals. At the same time the generation of spent catalysts has steadily risen due to new environmental regulations for low sulfur fuels and an increased appetite of gasoline consumers. This paper will examine spent catalyst market and the role played by Gulf Chemical & Metallurgical Corporation in the reclamation of metals over the last sixty years. Introduction Hydroprocessing (HDP) catalysts are used in petroleum refineries for two main applications: desulfurization and cracking. The catalyst support is alumina or mixtures of alumina and silica. Active metals include molybdenum, nickel, cobalt and tungsten. The selection of catalysts depends on the application and sometimes the cost. The life cycle of HDP catalysts is represented in Figure 1. The catalyst cycle in a reactor varies from continuous to one-two years. Catalysts used in various refining processes are deactivated by coke, sulfur, vanadium and other impurities in the refinery feedstocks and become spent. Refineries can optionally send the spent catalysts for regeneration, metals reclamation or landfilling. Catalysts used for refining heavy crudes often can not be regenerated. Catalysts used with light oils can be reused twice or three times after regeneration. When the option for regeneration is not viable, spent catalysts are send metal reclamation facilities or landfills."

Jan 1, 2008

By Artur Camposo, Rômulo. L. Loiola, Frederico M. Margem

"The growing interest for natural materials as an environmentally friendly alternative for the substitution of energy intensive and non-sustainable synthetic materials, has motivated the use of lignocellulosic fibers as reinforcement of biocomposites. The sisal fiber, a relatively unknown lignocellulosic fiber with potential for composite reinforcement, still needs to characterize for possible engineer applications. Therefore, the present work analyzed the sisal fiber by means of Fourier Transform Infra-red (FTIR) spectroscopy. The sisal fiber FTIR spectrum revealed main absorption bands typical of any lignocellulosic fiber. However, some specific bands as well as bands broadening and intensity suggested particular activities for functional molecular groups in the sisal fiber.IntroductionIn recent decades, environmental issues related to worldwide pollution and climate changes, mainly the global warming, are motivating new paradigms for the development of our society. Among these, the use of natural materials in substitution for non-sustainable synthetic materials, obtained from non-renewable ores and petroleum, is increasingly being considered. In particular, natural fibers extracted from plants are, in this 21st century, experiencing a surge as composite reinforcement [1-11 ], following their replacement by synthetic fibers, specially the glass fiber, during the second half of the 20th century [1-2-8].In addition to environmental benefits [12-13] the lignocellulosic fibers present economical advantages, such as worldwide abundance and comparatively low costs as well as some technical properties associated with flexibility and toughness[ll], which contribute to the performance of automobile components fabricated with natural fibers composites[14-16].Among the less common lignocellulosic fibers that only recently have been investigated[l 7], the fibers extracted from the stem of the sisal plant, shows in Fig 1, reveals a potential for polymer composite reinforcement."

Jan 1, 2013

By Felipe P. D. Lopes, Jr. dos Santos, Sergio N. Monteiro, Frederico M. Margem

"Continuous and aligned fiber composites provide the highest possible reinforcement for a polymeric matrix. In particular, the impact resistance is significantly increased in comparison with a low energy absorbed brittle polymer. For this reason, investigations have been carried out with both synthetic and natural fibers as a way to improve the toughness of polymeric composites. Among the natural fibers, ramie was not yet been studied for its reinforcement effect to make tougher polyester composites. Thus, the present work assesses the impact toughness of polyester composites incorporated with different amounts of ramie waste fibers.IntroductionIn most engineering and other technological areas, the use of materials associated with low energy processing conditions is gaining attention for the possible environmental benefits. This offered an incentive towards the substitution of natural renewable and biodegradable materials for the traditional energy intensive synthetic materials [1]. Natural fibers from both origins: animal, such as silk and wool, and vegetable, such as cotton and jute, are typical examples of those environmentally friendly materials. Low cost and highly reduced processing machinery wear are important advantages of the natural fibers over the most common synthetic ones such as glass fiber and nylon. For these reasons, polymeric composites reinforced with natural lignocellulosic fibers have nowadays been the subject of investigation [2,3].The mechanical strength is one important property of lignocellulosic composites to access the possibility of uses like structural materials for building parts such as doors and panels, as well as furniture. In this case, mechanically strong fibers like sisal, jute, curaua and ramie [4-7] are most convenient. Moreover, the relatively low fiber/matrix interfacial shear stress in these composites is associated with higher impact energy. In fact, a greater energy has to be expended for the rupture of a weak interface. The many cracks that are formed by impact tend to branch during the fiber pullout from the matrix [8]. A larger number of cracks correspond to a greater fracture surface and consequently higher toughness."

Jan 1, 2008

By C. Pereira

Spent nuclear fuel (SNF) can be treated in a molten salt electro refiner for conversion into metal and mineral waste fonns for geologic disposal. The fuel is dissolved in molten chloride salt. Non-transuranic fission products in the molten salt are ion-exchanged into zeolite A, which is subsequently mixed with glass and consolidated. Zeolite was found to be effective in removing fission product cations from the molten salt. Breakthrough of cesium and the alkaline earths occurred more rapidly than was observed for the rare earths. The effluent composition as a function of time is presented, as well as results for the distribution of fission products along the length of the column. Effects of temperature and salt flow rate are also discussed.

Jan 1, 1996