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By S. Aguayo-Salinas, J. L. Valenzuela-García, A. L. Leal-Cruz, M. I. Pech-Canul, M. T. Certucha-Barragán

"The aim of this research was to carry out a comparative and systematic study of the degradation of cyanide by hybrid natural/biodegradation and biodegradation methods using a mixture of Pseudomonas sp and Bacillus megaterium native bacteria. Bioreactors consist of filled columns with contaminated ore containing 100 ppm of total cyanide. In the biodegradation tests a mixture of bacteria was inoculated into the biodegrading solution. Results of cyanide degradation show a similar asymptotic behavior in both the hybrid (opened system) and biodegradation (closed system) methods; however, for the same period of time (72 h) the permissible maximum levels (1-2 ppm of cyanide) are only attained in the closed system. While in the closed system the cyanide levels are reduced from 100 to 1.5 ppm, in the open system, cyanide decreases from 100 to 2.4 ppm.IntroductionOne of the most important tasks of mining industry is the treatment of the wastes generated in mining operations. Accordingly, industrial waste waters and ores represent a complex problem and a great challenge. In addition to ethic and communitarian considerations, there are laws that prohibit or regulate the contamination of water and air. Moreover, they establish that the restoration of wastes must be considered as a necessary operation cost [1]. Currently this important problem is being addressed by the mining and metallurgical industries using different approaches; mainly they are focusing on the treatment of waste waters and ores generated by the leaching process in which cyanide is used as a leaching agent for the recovery of precious metals as gold and silver. Cyanides have toxic characteristics and thus negatively impact the environment when they are discharged to the ground without previous treatment. While there are some processes in current use there are others that have only been proposed and that allow cyanide degradation, transformation to less toxic compounds and/or the complete elimination of cyanide. The second group includes a variety of techniques that use natural, chemical and biological treatments. Natural treatments consist of the passive abandoning of the heap and of its washing with water. Since these processes are slow and generate great volumes of water partially contaminated, then other alternatives should be considered."

Jan 1, 2008

By Chris Twigge-Molecey

As emission constraints for metallurgical plants become more difficult to meet; control of major, multi-vessel, flue systems become more critical. Control instabilities can result in significant loss of system capacity or emissions to the environment. This paper will discuss the use of dynamic simulation techniques to optimize both the design and control strategies for these systems. A significant ,safety hazard is associated with pressure excursions from process upsets or equipment failures. Pressure rise rates of up to 10 kPajsec can occur. These cannot-be followed by conventional controls. Fail-safe high speed venting is required to protect both the furnaces and operating personnel'. Design options, sizing techniques and practical problems are discussed.

Jan 1, 1992

By Volker Uhlenwinkel

The design of a free fall atomizer as well as the process parameters affect the particle mass flux distribution in the spray cone. The mass flux distribution is important in spray forming because of its influence on the deposit shape and enthalpy input into the deposit. In this article the effect of different process parameters on the mass flux distribution is shown. Furthermore, different melts were atomized with the same atomizer. An empirical correlation will be introduced to predict the mass flux in the spray cone. This correlation will be compared with experimental results.

Jan 1, 1999

By Kunihiko Takeda, Kimio Imaizumi, Tsuyoshi Arai

"The study on the preparation of mono-dispersed liquid droplet was performed using ultrasonic as one of the steps of producing the perfectly mono-dispersed particle. The ultrasonic system was a 33.6kHz ultrasonic generator, an amplifier, an electric distortion element, and a bolted Langevin type horn installed in .a cell. For the first time, a liquid pillar under a nozzle of the cell ·was stably formed. Then, dense and coarse parts were alternatively constructed by oscillating the wavelength of the ultrasonic.· The diameter of those liquid droplets were found to be· perfectly uniform, therefore, it was measured by ""multiplex photography"" using a synchronized stroboscope with the ultrasonic.- From the results, more than 30,000 of perfectly uniform liquid droplets in 1 second were observed by this method.IntroductionRecently, research on the control of physical form is done in various fields of industry. Some examples are the processing technology of the minute compound material of micro-machines and integrated circuits, and the form control of molecule size like catalysts. There is a need for such material to take on various forms in correspondence to its use. ""Form control"" as used in this study will indicate ""research on physical chemistry factors which determine the size of the material"" and will refer to the contour uniformity of comparatively little particles. A well-known method of preparing particles is to spout a mist of liquid and slurry from a nozzle l) 2). Particles for metals, catalysts and food have been prepared by this method. In this case, although an approximate particle diameter can be decided by controlling the nozzle diameter and the violent outflow velocity, it is not easy to completely control ·the contour and to prepare a particle with uniform diameter. ·However, the preparation of perfectly uniform particles is necessary for solders for the adhesion of electronic wiring 3), ion exchange resins4), catalysts and so on. Large quantities of fine particles and super-fine particles are generated when manufactured in the usual way. Large quantities of these fine· particles and super-fine particles have polluted the internal and external' environments of factories. The products yield' ·decreases, also. From such a background, this study examines the preparation of perfectly uniform particles that could be· collected -100% as products. Recently, NASA has succeeded in the preparation of perfectly uniform particles in zero gravity 5). But the preparation of 'perfectly uniform particles by this method is difficult, and it can not be used in general industry"

Jan 1, 2000

Laboratory trials were performed in an induction furnace to study droplet formation during lance blowing. Compressed air was blown on a molten iron bath consisting of iron alloyed with carbon and silicon. Steel droplets were collected using a specially designed sampler. The average steel droplet composition and the oxide layer thickness were determined using scanning electron microscopy combined with energy dispersed spectroscopy. In addition, the concentration gradient of elements was determined using a microprobe. It should be noted that a special technique had to be developed in order to prepare the droplet sample. The size distribution and composition of the droplets was also determined using the microprobe. It was found that the carbon content in the droplets was lower than the carbon content in the bulk.

Jan 1, 2006

By A. W. Bryson, S. P. Fox, S. A. Godorr

"This work is an extension of a previous investigation on the development of surface roughness during electrodeposition of copper. A comprehensive model based on diffusion and migration in a force field together with surface diffusion and sticking probabilities is used to generate profiles which are compared to those produced experimentally. The roughness is characterized by using the technique of fractal geometry which is shown to describe both qualitatively and 9uantitatively the development of surface morphology during electrodeposition.The work is extended to the deposition of copper in the presence of various concentrations of thiourea. The development of roughness is observed experimentally on the edge of a thin copper disc mounted between two glass plates. This enables photographs to be taken at various stages during growth. The surface outline is digitized using an image analyzer which enables the fractal dimension to be determined as growth proceeds. As expected, the presence of thiourea at low concentrations produces a fractal dimension which is closer to unity (i.e. the surface becomes smoother).IntroductionThe development of surface morphology during electrodeposition has far-reaching implications for copper plating in the electrowinning and electrorefining processes. Short circuits as the cathode surface grows unevenly require operator intervention in a dangerous environment and imply processing delays, and the inclusion of electrolyte in small gaps in the plated cathode have implications in downstream processing of the cathode. Higher current densities are obviously desirable, as they result in greater production rates, but as shown by Ettel et. al.(l), Harvey et. al.(2), Cook (3), and Harvey et. al.(4), it is not possible to operate near the projected economically optimum conditions because the electrodeposition of copper from sulphate and acid solutions is a mass transfer controlled process. It has been shown (Ettel et. al.(l), Harvey et. al.(2)) that the closer a system operates to mass transfer limiting conditions, the poorer the resulting cathode quality. One solution is to use agitation techniques to increase the limiting current density. Another is to add surface active additives to the electrolyte which has been shown by Ettel et. al.(l), Harveyet. al.(2) and Afifi et. a1.(5) to allow higher rates of production without decreasing cathode quality. The second proposed solution is of interest in this work, since there is very little knowledge of the conditions under which these additives operate effectively, and little fundamental understanding of the mechanism by which they operate. The current work seeks to contribute to this field by correlating a simulation model with experimental results to describe the development of surface morphology in the electrodeposition process."

Jan 1, 1997

By Kim Fagerlund

Boliden Harjavalta Oy operates a copper smelter in Finland, which is based on flash smelting together with Peirce-Smith converting of copper matte. This paper reviews a case study when a high arsenic feed mixture was successfully eliminated in order to guarantee the anode quality. Based on theoretical and practical knowledge in slag chemistry at Outokumpu Research, the CaO-fluxing practice was introduced. Description of a thermodynamic simulation using MTDATA and implementation of the results into converting practice is given. Results showed that the impurity fluctuations in raw materials could be effectively controlled by efficient utilization of different slag chemistry.

Jan 1, 2005

By Toshio Kurikami, Koichi Yamazaki

"Toho Zinc Co., Ltd Chigirishima Refinery has the production capacity of electrolytic lead for 95000t/y by sintering- blast furnace electrolytic process. Lead raw materials are lead concentrates, spent batteries and dusts that contain lead from other companies, and these are handled by existing smelting process. There are many circulation materials in the process, because the system has been constructed with improving the recovery rate and protecting the environment. This report describes material balance in each process, distribution of the lead and various components, and it examines present state of the processing. In addition, we report the result that we have tried to improve the work environment.IntroductionThe Chigirishima Refinery of the Toho Zinc Co., Ltd. is located in Chigirishima, an island 4km off the coast of Takehara-city, Hiroshima, Japan. The Chigirishima Refinery began lead smelting operations in 1951.The Chigirishima Refinery adopted the sintering-blast furnace-electrolytic process and has an electrolytic lead production capacity of 95,000 tons/year. The existing smelting process handles raw materials from lead concentrates, spent batteries, and lead-bearing dust from other companies. This system was constructed with the intentions of improving material recovery ratios and protecting the environment; therefore, there are many materials recirculating throughout the smelting process. This report describes the material balance in each process and the distribution ciflead and various components, and it examines the present state of processing. In addition, we report the results of our attempts to improve the work environment."

Jan 1, 2000

By Luciano R. G. Santos

Keywords: biosorption, cadmium, copper, biomass, spent zeolite. The majority of the industrial activities produce some kind of solid wastes. In this work two industrial residues (spent zeolite and wood sawdust) were chemically modified to increase their heavy metals sorption capacities. Manilkara longifolia (a Brazilian plant known as parajú) sawdust was first treated with NaOH and modified with different citric acid concentrations (0.6-1.2 mol/L) at 120°C, for 90 min. Infrared spectroscopy confirmed the presence of carboxylate groups in the wood structure as result of their mixing. Similarly, spent zeolites were also submitted to a chemical treatment (NaOH) to remove carbon deposited during oil cracking and to recover its sorption capacity. Batch experiments carried out at ambient temperature showed that both materials present sorption capacity for copper and cadmium comparable to weak acid ion exchange resins. A maximum of 78 mg-Cd/g and 59.7 mg-Cu/g as well as 29.9 mg-Cd/g and 14.6 mg-Cu/g were observed for the sawdust and the zeolite, respectively. The results were modeled according to the Freundlich and Langmuir equilibrium isotherms and compared with results of other studies.

Jan 1, 2005

By Sun Ying, Zhang Jing, Li Qiu-ju, Wang Yan-ze

Copper smelter slag was leached using sulphuric acid solutions under atmospheric conditions. Base on the composition and phase of copper slag, the effect of the concentration of sulfuric acid and leaching temperature to the leaching growth rate of Fe, Cu, Co and Ni in the copper slag were investigated in this paper. Simultaneously, the influence of sulfuric acid concentration, leaching time, leaching temperature and the amount of sulfuric acid (solid-liquid ratio) to the leaching rate of these metal elements were researched. Experimental results showed that: with the increasing temperature, the dissolution rates of the metals elements increased first and then decreased. Due to the influence of silica gel which was obtained in beginning of leaching, the higher the concentration of sulfuric acid is not conducive to dissolution of the valuable metal elements. The dissolution degree of Fe, Cu, Co and Ni were 92.83% 96.76% 93.62% and 63.41% respectively.

Jan 1, 2016

By Wenying Liu

The effect of aeration on chalcocite heap leaching was studied by analyzing the historical data from two chalcocite heap leach pads located in Chile, one with aeration and the other without aeration. The data showed that the copper leaching kinetics of the aerated heap was greater than that of the unaerated heap within a certain leaching period, after which there was no effect of aeration on the copper leaching kinetics. The total acid consumption per ton of ore processed was higher in the case of aeration, which was supported by the higher pH of the PLS. But the net acid consumption per ton of copper produced was the same in the two cases. Approximately 5% of the total iron added to the unaerated heap was precipitated inside the heap. In contrast, there was no net iron precipitation or generation inside the aerated heap. Bacteria activities were thought to occur even in the unaerated heap, but the extent was much less than in the aerated heap. Given the importance of forced aeration in chalcocite heap bioleaching, mathematical modelling will be applied in the future work to assist the optimization of the aeration system design.

By Edouard Asselin, Guikuan Yue

"In the present study, electrochemical measurements, especially cathodic potentiodynamic polarization (CPC) and cyclic potentiodynamic polarization (CPP), have been employed to study the kinetics of ferric reduction on chalcopyrite in aqueous Fe( II )-Fe(III)-H2S04 solution at 25°C and 70 °C. Results from the calculation ofspeciation in the above solution reveal that, at both 25 °C and 70 °C, the real Fe3+/Fe2+ ratio is much lower than the nominal ratio, which leads to smaller values for the reversible potential of the ferric/ferrous couple based on the Nemst equation. Exchange current densities of the ferric/ferrous couple were obtained by extrapolating the cathodic linear Tafel line to the reversible potential and are on the order of 10-7·10-6 A/cm2 at 25°C and 10·6-10-5 A/cm2 at 70 °C, respectively. The transfer coefficients were about 0.35-0.38 at 25°C and 0.35-0.45 at 70 °C. Polarization plots of CPC and CPP under different nominal Fe3+/Fe2+ ratios are in good agreement at 25 ·c and at 70 °C. Based on the obtained exchange current densities, the rate constant k, was calculated and is on the order of 10-1 cm/s at 25 °C and 10 1 cm/s at 70 °C.IntroductionChalcopyrite is the most abundant copper mineral in nature, accounting for about 70% of copper reserves in the world [I]. In recent years, the metallurgical industry has been searching for a hydrometallurgical process as an alternative to pyrometallurgical treatment due to high emissions of S02 and capital costs associated with smelting. Activity in this area has increased recently due to some inherent advantages associated with hydrometallurgical processing, such as the possibility of treating low-grade ores (increasingly more abundant in the case of copper) and easier control of waste, with the attendant benefits to the environment [I]. Chalcopyrite is highly refractory under most hydrometallurgical conditions, owing to the formation of an anodic passivation layer on the chalcopyrite surface which renders the process kinetics very slow. Most of the currently proposed processes are based on sulfuric acid with ferric ions and/or dissolved oxygen as oxidants. Sulfuric acid is preferred over all other leaching reagents in terms of cost, environmental friendliness, and ease of its regeneration during electro-winning. Some of these processes have been piloted in attempts to implement these technologies on an industrial scale,"

Jan 1, 2012

By J. Antrekowitsch

Keywords: residues, fluorides, chlorides, zinc, steel mill dust The recyclability of various nonferrous metal wastes often suffers from a relatively high fluorine and chlorine content. Both are inserted in most cases by the use of plastic contaminated scrap and a wide variety of different coatings. These halogens lead to poor product qualities and off gas contamination. Especially the history of zinc recovery from steel mill dusts shows, that the today common hydrometallurgical options are on their limit and therefore are not sufficient in most cases. This thermochemical study should give more information about different pyrometallurgical options, that offer both a chlorine and fluorine reduction and efficient zinc recovery, preferably in one process step. Selective evaporation in different atmospheres and conversion with the use of hydrogen are the main parts in this study. The results combined with the relatively small information available from literature should provide a basis for further investigations in this field.

Jan 1, 2005

By Qingyun Huang, Wei Lv, Junyi Xiang, Xuewei Lv, Chenguang Bai

The kinetics of iron leaching from ilmenite in hydrochloric acid solutions were investigated. The effects of pre-oxidation roasting, leaching temperature, and holding time on iron extraction rate were determined. The results obtained show that the extraction of iron is significantly enhanced by pre-oxidation roasting and increasing leaching temperature from 75 to 108 °C. The results of the kinetic analysis of the leaching data indicate that the reaction is controlled by diffusion through the product layer. The apparent activation energy for the extraction of iron has been calculated to be 62.5 and 55.1 kJ/mol for untreated and oxidized ilmenite, respectively.

Mar 1, 2018

By C. R. Palmer

The Bureau of Mines investigated the use of ion-exchange technology for the recovery of precious metals from cyanide leach and spent electrolytic solutions. This research included adsorption of gold and silver on both weak-and strong-base anion-exchange resins. The effects of nickel, mercury. and iron on precious metal loading of strong-base resins were also determined. Due to the nonselectlvity of strong-base resins, selective elution also was investigated. Both commercially available and experimental weak-base anion-exchange resins were tested. None of the commercial weak-base resins tested were suitable for a caustic-cyanide system owing to their low recovery of precious metals at pH 10 or above; however, three experimental resins have possible application. Continuous tests conducted with mill cyanide solution in a multicompartmented ion-exchange column using strong-base anion-exchange resins adsorbed nearly 100 pct of the precious metals as well as the iron and nickel. During the elution of this loaded resin the iron was first removed with NaCI plus NaOH; then nickel with dilute H2S04 or HCl; finally gold and silver with thiourea in dilute HCl.

Jan 1, 1988

By A. Tsubouchi, F. Noguchi, T. Takasu

"A high current density operation is desired to improve the productivity in copper electrorefining. However, a lot of problems still remain such as passivation at anode, dendritic deposition at cathode and impurity behavior during the electro refining.Effects of the current densitY on the morphology of copper deposition on the cathode, and passivation at the anode were investigated at various fluid velocity of electrolyte in the present study.Although a granular appearance of the copper deposition was obtained with increasing high current density, it was depressed by an increase of the fluid velocity of the electrolyte. A uniform deposition on the cathode was also observed when the fluid velocity of the electrolyte become higher. It was ascertained that passivation at the anode was suppressed by circulating electrolyte during electrolysis. INTRODUCTIONIt is desirable to operate at high current density in copper electrorefining in order to improve plant productivity without enlarging the size of electrodes(1). However, there are many problems in copper electrorefining at high current density with the usual commercial practice, for example, anode passivation, dendritic deposition and an increase of impurities in the cathode.In general, it is effective to agitate the electrolyte in order to suppress these problems(2). Smith et a1.(3) have performed electro refining experiments at various current densities in the range of 8 to 32 Aldm2 and at electrolyte fluid velocities in the range of 40 to 120 mlmin, and they obtained well consolidated, void free copper even at high current density in a high electrolyte velocity. However, they did not discuss the recovery ratio and the passivation behaviour at the anode. Walsh et a1.(4)(5)(6) experimented with the rotating cylinder electrode, and ascertained that electrolysis can be carried out at high current densities under the condition of pure electrolyte.With regards to anode passivation, there are several papers by previous workers(7)(8). Our group ascertained the process of producing anode slime during electrolysis(9). However, these experiments were carried out without forced circulation of electrolyte. Therefore, in the present study, to solve these problems, we electrolyzed at current densities in the range of 4 to 50 Aldm2 with circulating electrolyte in the range of 0 to 48 mlrnin. The effect of electrolyte fluid velocity on the surface morphology of deposited copper at cathode and passivation at anode were investigated when electrolysis were carried out with circulating electrolyte at high fluid velocity and at high current density."

Jan 1, 1997

By J. C. Huyhua

The effect or various oxidants on gold and silver dissolution in thiourea solutions (0.05 M in H2SO4) was studied using the rotating disc technique, a.t 2s c and 600 rpm. These studies were carried out at constant (4:1) initial molar ratio or thiourea to oxidant concentrations, to produce 50 % thiourea. oxidation. The initial dissolution rate of gold was approximately four times higher in the presence. of ferric sulfate (5.37 x 10-3mg cm-2 s-1) than in the presence of hydrogen peroxide (H2O2), potassium persultate (K2S2O3), or monopersulfa.te (KHS06). The dissolution rates for silver were considerably lower than gold for the same oxidants. Oxidation of thiourea in the presence of peroxygen and persulta.te compounds is a. fast reaction and it is completed in less than ten minutes. On the other hand, the oxidation or thiourea with? ferric.sulfate is slow, yielding a second-order reaction rate constant k = 6.09 I mol-1 h-1. Sulfur formation in the ferric thiourea system begins when ferric ion reduction approaches to completion. With hydrogen peroxide, sulfur is observed at lower thiourea concentration than ferric. Suifate. The presence of a large excess or free thiourea i.e., s to 20 % thiourea oxidation) retards sulfur formation and maintains favorable dissolution rates. Finally, carbon-in-leach experiments indicate that thiourea solutions a.re stable for several days, with ferric sulfate or hydrogen peroxide. The dissolution rates of gold and silver doubles in the presence or activated carbon when hydrogen peroxide is used as oxidant.

Jan 1, 1989

By Yotamu Stephen Rainford Hara, Animesh Jha

The investigation focuses on a low temperature recovery of Cu and Co from a 40 wt% SiO2-(30 wt%Fe,6 wt%Al)2O3-10wt% CaO-7wt%CuO-7wt%CoO slag over a temperature range of 1173K to 1323K. The alloy phases containing Cu-Co and Fe-Co alloy formed via the carbothermic reduction of oxides: MO + C = M + CO(g), where M represents metallic copper, cobalt or iron. In the direct reduction of oxides, the recovery of metallic phase was well below 90% at 1323K, due to the kinetic barrier which was analysed and attributed to oxygen and metal-ion transport in the slag. This barrier was overcome by adding CaSO4 and carbon, which yields a matte (MS) phase via MO + CaSO4 + 4C = MS + CaO + 4CO reaction. Lime thus produced in situ participates in metal oxide/metal sulphide reduction reactions, which are analysed with the help of X-ray powder diffraction, scanning electron microscopy, and thermogravimetric analysis.

Jan 1, 2014

By Michael A. Krstich

A soil washing pilot plant to treat soils at the U.S. Department of Energy (DOE) owned Fernald Environmental Management Project (FEMP), was designed based on extensive bench-scale testing. The system's design incorporated a combination of physical separation and' chemical extraction processes and was tested on two soils. The textural composition of the two soils was approximately 20 percent sand, 60 percent silt, and 20 percent clay. Since this grain size distribution was not considered optimum for physical separation techniques, thesoil washing pilot plant had to be designed with selected equipment to provide specific soil size fractions during processing operations. A trommel, vibrating screen deck, centrifuge, and attrition scrubber were used in the system to selectively separate specific soil size fractions at 4.75, 2, 0.3, and 0.02 millimeters (mm). The trammel used high pressure water [1000 pounds per square inch (psi)] during the initial step of the process to reduce soil aggregates to single grain composition, separate out greater than 4.75 mm gravel, and dislodge chemical contaminants from the individual soil particles. The vibrating double-screen deck provided 2 - 4.75 and 0.3 - 2 mm soil fractions that, when combined, averaged greater than 75 percent solids for both soils. The centrifuge was designed to take the less than 0.3 mm soil slurry from the screen deck and produce a particle size of 0.02 mm. The centrifuge produced a high solids stream that averaged greater than 70 percent solids for both soils. These 0.02 to 0.3 mm soil solids from the centrifuge were combined with the 0.3 to 4.75 mm soil solids from the screen deck and processed through the attrition scrubber. The data collected from the pilot-plant operation was used to aid in the design of a full-scale system and was instrumental in formulating full-scale process operations and the selection of equipment.

Jan 1, 1995

By J. P. Downey, L. G. Twidwell

"The high density sludge process (HDS) is a commercially proven acid rock drainage wastewater treatment process that is based on acid neutralization and metal precipitation. Previous studies have established that metal removal efficiencies in precipitation-based wastewater treatment applications can be improved through metal ion adsorption on ferrihydrite and/or aluminummodified ferrihydrite. This study was conducted specifically to determine whether the metals removal efficiencies at an existing industrial facility could be improved by promoting ferrihydrite and/or aluminum-modified ferrihydrite precipitation during the pH adjustment stages of the HDS process. The metal tenors of the treated wastewater samples are compared with those obtained through baseline experiments, which were designed to simulate the conventional HDS operation. The subject metals were: aluminum, arsenic, cadmium, copper, iron, manganese, nickel, and zinc.IntroductionThe HDS process is commercially proven ARD wastewater treatment technology that involves raising the wastewater pH by adding hydrated lime, caustic soda, or another alkaline substance. In addition to neutralizing the acidity, many dissolved metals precipitate as pH is elevated. Waste volume is minimized by capturing and immobilizing the precipitated solids.However, ARD streams characteristically contain multiple dissolved metal species. The response of various metals to pH adjustment in the HDS process is neither uniform nor quantitative, so minor to trace concentrations typically remain in the treated wastewater following solid-liquid separation. The effectiveness and applicability of the process would be improved if a means were found to further reduce the metal concentrations.Previous research and industrial applications have proven that metal ion adsorption on ferrihydrite (FH) and/or aluminum-modified ferrihydrite (AMF) increase metal removal efficiencies. Ferrihydrite and AMF are considered ideal for cation and anion adsorption from an aqueous solution at the appropriate pH [1]. Ferrihydrate adsorption of dissolved heavy metals is widely practiced throughout the world [2, 3]. It is established that FH and AMF effectively adsorb As contained in aqueous solutions [4]. Arsenic removal by adsorption on FH is the U.S. Environmental Protection Agency’s (EPA) Best Demonstrated Available Technology [5]. Twidwell and Leonhard also demonstrated that heavy metals (Cd, Cu, Ni, and Zn) are effectively removed from solution by coprecipitation/adsorption using AMF and FH [6]."

Jan 1, 2008