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By Brady Butler

Many high capacity metal hydrides exhibit a high degree of stability in the hydrogenated state. This stability leads to a number of significant design problems with regard to the low temperature kinetics and thermodynamics of dehydrogenation. Nanometric metal hydride materials provide a promising route for increasing the reaction kinetics while altering the thermodynamic stability of the material. The use of nanometric metal hydride materials for hydrogen storage has largely been absent because of the difficulties associated with the synthesis of these materials. In this paper, research results on the synthesis of lithium based metal hydrides by vapor phase reactions are presented. The lithium based compounds that have been made in our lab include nanosized powders of metallic Li, Li₃N, LiNH₂ and LiH. The vapor phase process has also been used to custom engineer Li-based materials with other alloying elements or doping elements. The dependence of the characteristics of these materials on synthesis process parameters is studied. The effects of nanoscaled particle sizes on the kinetics of dehydrogenation and hydrogenation reactions are also explored.

Jan 1, 2006

By Marco Pasetto

The possibility to re-use marginal materials (by-products) deriving from industrial activities in the construction of road infrastructures, as total or partial substitution of natural aggregates, successfully combines demands for economy and environmental sustainability. The paper presents the results of a laboratory study, conducted at the Experimental Road Laboratory of the University of Padova, to verify the suitability of a particular type of electric arc furnace slag to be recycled in the lithic skeleton of high-performance asphalt mixes (porous asphalt, high modulus mixes, stone mastic asphalt, nonskid surfacings) for road and airport flexible pavements. the process of transformation of iron and steel slag into a product that can be used in road building is described, along with the characterisation of the mixtures, plus an analysis of the results of a wide battery of mechanical-performance tests. This study forms part of wider theoretical ? experimental research being done at the University of Padova in order to improve knowledge of the characteristics of succedaneum materials and check their possible applications in road and airport construction.

Jan 1, 2006

By Heikki Jalkanen

Oxygen converting of hot metal (LD/BOF) is contemplated as an object of simulation. Oxygen converting is a highly complex thermo-chemical process comprising a series of matter and energy transformation and transportation steps that makes the simulation very challenging. The basic principles of CONSIM 5 oxygen converter simulator are presented. Simulator is a comprehensive combination of a physical model with several empirical submodels describing all properties and processes that affect the final result of a converter blow, final mass and composition of steel, slag, dust and converter gas as well as the end temperature of steel. CONSIM simulator is used for simulation of series of high and low carbon steel blows. Simulated steel temperatures, oxygen consumption, blow time and iron oxide content of slag are compared with measured values. Problems of simulation and requirements for quantitative simulation of oxygen converter process are discussed.

Jan 1, 2006

By Kazuya Koyama

We are studying the hydrometallurgical recycling process of indium from an Indium-Tin-Oxide(ITO) target. For this process, it is necessary to remove Sn(IV) ions from the aqueous hydrochloric acid solutions containing In(III). In this study, the removal of Sn(IV) ions by a potentiostatic electrolysis method was examined. The polarization measurements and potentiostatic electrolyses were carried out under a nitrogen atmosphere. In the Sn(IV) solution, current begins to rise at the cathode potential of -0.26 V vs. SHE, and increases with a reduction in the cathode potential. In the In(III) solution, current begins to rise at a cathode potential of -0.43 V vs. SHE. Metallic tin was electrodeposited without indium electrodeposition at the cathode potentials of -0.30 and -0.40V vs. SHE. More than 98% of the Sn(IV) was removed at the cathode potential of -0.40 V after the electrolysis for 3hrs. Both tin and indium were electrodeposited at the cathode potential of -0.50V vs. SHE.

Jan 1, 2006

By Ian M. Ritchie

Cementation or metal displacement reactions such as Cu2+ + Fe Cu + Fe2+ are among the oldest known hydrometallurgical reactions. They are still used in the recovery of some metals and in the purification of process liquors and waste water streams. However, they are often more complex than the stoichiometric reaction would suggest because they involve the simultaneous deposition of one metal onto a second which is dissolving. For example, sometimes a cementation will not take place, even though it is thermodynamically favoured. On other occasions, a cementation reaction will start but come to a halt as the depositing metal blankets the reacting surface. On yet other occasions, side reactions, catalyzed by the deposit, can be important. In this paper, the electrochemical basis of cementation reactions is described. The conditions for each of the complications encountered in these reactions are described and illustrated by examples drawn from a number of hydrometallurgical processes. The cementation reaction between activated carbon and gold thiosulfate is also briefly described, this reaction being unusual in that no dissolution of the carbon occurs.

Jan 1, 2003

By Ian M. Ritchie

Cementation or metal displacement reactions such as Cu2+ + Fe Cu + Fe2+ are among the oldest known hydrometallurgical reactions. They are still used in the recovery of some metals and in the purification of process liquors and waste water streams. However, they are often more complex than the stoichiometric reaction would suggest because they involve the simultaneous deposition of one metal onto a second which is dissolving. For example, sometimes a cementation will not take place, even though it is thermodynamically favoured. On other occasions, a cementation reaction will start but come to a halt as the depositing metal blankets the reacting surface. On yet other occasions, side reactions, catalyzed by the deposit, can be important. In this paper, the electrochemical basis of cementation reactions is described. The conditions for each of the complications encountered in these reactions are described and illustrated by examples drawn from a number of hydrometallurgical processes. The cementation reaction between activated carbon and gold thiosulfate is also briefly described, this reaction being unusual in that no dissolution of the carbon occurs.

Jan 1, 2003

By Hai-Xing Fang, Chao Liu, Tao Zhang, Bing Xie, Hong-Yi Li, Cui Li

"Hongge Ore, a kind of vanadium-titanium magnetite ore containing high content of chromium, is valuable resource for extracting Fe, V and Cr in China. During present processing of the ore, vanadium and chromium were both concentrated in slag, leading to higher content of chromium in the vanadium slag than that of common one in Pan-Steel. Mineral phases and characteristics of spine! crystals, which influenced greatly subsequent roasting process, in the vanadium slag under different cooling conditions were investigated by using XRD and SEM/EDS. Results showed that vanadium slags containing various contents of chromium were composed of spine!, in which V and Cr were both concentrated, olivine and pyroxene. Growth rate of spine ls decreased sharply below 1350°C. The non-isothermal crystallization process could be described by modified Avrami equation and Ozawa equation. Avrami exponent and Ozawa index were calculated and growth mechanism of spine! crystals was discussed.IntroductionVanadium (V) as well as chromium (Cr) is important non-ferrous metal widely used in materials and chemical industries [1, 2]. Especially, both of them are important alloying elements for the production of high alloyed steels to achieve desired physical-chemical and mechanical properties. Vanadium-titanium magnetite ore in Panzhihua-Xichang area (China) is an important raw material for extracting vanadium. During the extracting process, vanadium is firstly reduced into hot metal and then concentrated in slag phase by blowing oxygen into the hot metal in converter [3]. This kind of slag containing 5~20 wt% V20 3 are usually roasted with sodium or calcium salts and then leached to obtain vanadium containing solution and final products. Current vanadium slag obtained from normal vanadium-titanium magnetite ore contains low content of Cr20 3 and chromium extraction is thus ignored. However, chromium content in the vanadium slag would be increased intensively when the Hongge Ore used, which is also important vanadium titanium magnetite in Panzhihua-Xichang area containing 0.2~0.8 wt% Cr203. Therefore, this kind of vanadium slag with high content of chromium would also be important sources for vanadium and chromium extraction. According to previous work [4], both vanadium and chromium could be extracted from vanadium slag with high content of chromium by salt roasting and leaching, which is illustrated in Fig.1."

Jan 1, 2013

By Jeong-Hwan Kim

The liquid-liquid reactive process (solution process) is often adopted as a synthetic method for precipitated calcium carbonate (PCC) in laboratory studies for its simplicity in operation or ease in controlling process variables. Still, PCC are produced commercially by passing carbon dioxide through a milk of lime, i.e., by a gas-liquid reacting method (carbonation process). Few studies on the carbonation process have been conducted, since the process variables are interrelated and difficult to control compared to the solution process. In this study, both carbonation and solution processes were employed to study the polymorphs of calcium carbonate and growth rate of PCC crystals. The effects of the characteristics of limestone ores as a raw material in the synthetic system of PCC on the synthetic characteristics of PCC were also investigated. To control the nucleation rate in the synthetic systems, the shape factor was considered most important. Single-phase aragonite PCC could be synthesized under a variety of controlled experimental conditions such as ionic strength, solution composition, concentrations of additive ions, and temperature.

Jan 1, 2006

By A. Dell’Era, M. Pasquali, C. Lupi

"An electrochemical cell has been designed to treat very diluted cobalt solutions, i.e. those deriving from recycling processes of lithium-ion batteries. A reticulated vitreous carbon sponge was used as cathode and a Pt-coated Ti net as anode. A controlled potential electrolysis has been carried out in a solution flowing in the cell and maintained at a constant pH of 6.5. Considering the cathode dimensions (10.0 cm * 10.0 cm * 1.25 cm), rather high volumes of solution (>1 litre) can be treated with flow rates up to 1.6 l/min. The process yield is obviously related to the solution concentration; it has been observed that, starting with a solution containing 200 ppm of Co2+, the yield is initially ~35-40%, but it decreases to ~20% when 80% of the initial cobalt content has been electrowon. The yield increases up to ~50% if the carbon electrode is coated by cobalt. The conditions allowing a fast and complete removal of cobalt are outlined. Introduction Industrial liquid effluents containing heavy metal ions arise not only during hydrometallurgical processing, but also in many sector of chemical industries utilizing metal catalysts and process reagents. These waste solutions containing low quantities of metallic ions can be treated by chemical precipitation, solvent extraction, ion exchange, etc. before final discharge. All these techniques could be efficient for complying the aqueous effluents with the severe rules related to the environmental impact, but they can not directly produce metals. Particularly the chemical precipitation presents two main drawbacks, huge amount of sludge prodction and reagent costs to produce this useless and sometime dangerous sludge that have to be considered. Electrochemical technologies can be used for the treatment of effluents polluted by metal ions, showing the following advantages in comparison with other processes: 1. recovering of the polluting substances in metallic forms, with subsequent reusing; 2. absence of process slag, which should be subsequently disposed of. In this work an electrochemical reactor with a reticulated vitreous carbon cathode and a platinated titanium net anode has been designed and utilized for removal Co from waste aqueous solutions. Porous materials have been used as electrodes for this cell, as their high specific surface area favours the treatment of these low metal content solutions (1-7). This kind of electrodic material presents very interesting chemical-physical characteristics such as: low density, low thermal expansion and high electrical and thermal conductivities; particularly the reticulated vitreous carbon (RVC) presents a very elevated void volume, rigid structure, good resistance to temperatures in non-oxidizing environments and very low resistance to fluid flow."

Jan 1, 2008

By M. J. Adam

As part of its research program, the U.S. Bureau of Mines is investigating the partitioning of complex minerals to simpler phases using sulfidation reactions for selective extraction of mineral constituents of value from extraneous elements early in processing schemes. This report describes research in which thermal processing of the complex Ti -bearing mineral ilmenite (FeTiO, ) resulted in partitioning of the valuable Ti metal to the simpler compound rutile (Ti0 ). Samples of ilmenite were blended with elemental S for thermal treatment a2 various temperatures under controlled atmospheres in an effort to dissociate the Fe from the ilmenite complex. Product characterization revealed that the Fe was partitioned from the ilmenite, forming a rim of pyrrhotite/pyri te (FeS/FeS,) on a rutile core. The products were agate milled and then subjected to cursory magnetic and flotation techniques in an attempt to physically separate the partitioned phases. Partitioning results and phase concentration data are reported relative to thermal treatment variables and physical separation techniques.

Jan 1, 1993

By Li Chen

A new process, i.e. Ball milling--Neural leaching--Oxidation calcinations--Chloridizing distillation--Hydrolysis, was designed to recover germanium from the vacuum furnace slag produced in Shaoguan smelter. The suitable process and operational parameters were determined for the practical production.

Jan 1, 2005

By Vinay Kumar, Jae-Chun Lee, Rakesh Kumar, Manis Kumar Jha, Archana Kumari, Pankaj Choubey

Present work is a part of developing novel recycling technique for waste printed circuit boards (PCBs) i.e. the liberation of metals from PCBs by organic swelling followed by the treatment of resin to remove/ recover hazardous soldering materials. In order to recover the hazardous metallic constituent lead from the liberated resin, initially the leaching studies were made using fresh solder containing 63.9% Pb and remaining tin. Experimental results obtained in different conditions viz. time, temperature and acidity showed -97.20% of lead dissolution with 6M HNO3 at solid to liquid (S:L) ratio 1:10 (g/mL) and temperature 90°C in 75 minutes. The result of the studies validated with crushed PCBs shows that almost total lead and tin was leached out with 6M HNO3 and 6M HC1 respectively at S:L ratio 1:10 (g/mL) and temperature 90°C within 50 minutes. The results will be useful for the treatment and safe disposal of PCBs resin.

Jan 1, 2011

By Gjergj Dodbiba, Toyohisa Fujita, Takahiro Kikuchi, I-Chen Wu

"In order to separate molybdenum (Mo) from the high-level radioactive liquid waste (HLLW), Pb-Fe based adsorbents were synthesized. The adsorbents were precipitated by adding sodium hydroxide in mixture of 1 mol/L lead nitrate and 1 mol/L ferric nitrate aqueous solutions. Each precipitate was then filtered, dried and ground to obtain a fine powder, which has been used as an adsorbent. Two main parameters were considered when synthesizing the adsorbents, i.e. the pH value at precipitation of adsorbent precursor and the calcination temperature of Pb-Fe based adsorbent. Moreover, the structures of the synthesized adsorbents were investigated by means of an X-ray diffractometer.The experimental results indicated that the calcination temperature of the Pb-Fe based adsorbent has a great influence on adsorption capacity of the adsorbent for Mo. It was found that when the Pb-Fe based adsorbent was calcinated at 500 oC, the sorbed concentration of Mo was the highest.1. IntroductionThe high-level radioactive liquid waste (HLLW), arising from the reprocessing of nuclear fuel are generally immobilized in an alkali borosilicate glass matrix. Broadly speaking, alkali borosilicate glasses are the matrix of choice for the immobilization of the HLLW, since they permit vitrification of waste stream of variable composition, [1]. Within this frame, the incorporation of molybdenum (Mo) is of particular interest in the vitrification of HLLW. Molybdenum is know to have a low solubility in borosilicate glass compositions and its presence in excess results in the phase separation of a complex yellow molten salt during vitrification, [1]. The formation of so-called “yellow phase” material during the vitrification process is undesirable since it leads to the accelerated corrosion of the inconel crucible liners. Furthermore, the “yellow phase”, which is reported to contain also other fission products, is soluble in aqueous solution providing a potential route for the leaching of radionuclides from the vitrified waste, should it come into contact with water, [1]."

Jan 1, 2008

By Ehsan Vahidi, Fereshteh Rashchi, Ataollah Babakhani, Alireza Zakeri

"The synergistic effect of Cyanex 302 on solvent extraction of nickel and cadmium from sulfate solution with D2EHPA diluted in kerosene was investigated with the aim of increasing separation efficiency. Experiments were carried out within a pH range of 0.1-5.0 using sole D2EHPA and D2EHPA-Cyanex 302 mixtures in different ratios. Increasing Cyanex 302 to D2EHPA ratios in the organic phase caused a left shifting of the extraction isotherm of cadmium and a right shifting of the extraction isotherm of nickel. As a result, optimum separation was found with a Cyanex 302 to D2EHPA ratio of 0.1M:0.5M. In the present system, effect of a modifying reagent such as TBP was studied. The influence of various diluents including kerosene and carbon tetrachloride was also investigated.IntroductionBatteries are popular sources of portable energy. Ni-Cd batteries are manufactured in two main groups of small domestic cells and large industrial batteries with 80% being in domestic use. Ni-Cd cells have various uses, for example in cordless electric utensils, cordless telephones, airplane engine starters, and communicational distribution systems [1].Depleted Ni-Cd batteries are classified as hazardous waste since nickel and cadmium are heavy metals and suspected carcinogens. Given the risk associated with uncontrolled disposal, directions for issuing legislation on disposal and recycling of used batteries have been made in industrialized countries [2]. Recycling of Ni-Cd batteries is important from both economic and environmental points of view. Different methods have been used for recycling these wastes through pyrometallurgy [3], biotechnology [4,5], and hydrometallurgy [1,2].Due to the advantages of hydrometallurgical processes, several studies have been implemented on leaching and solvent extraction (SX) of the used Ni-Cd batteries. Leaching of batteries is usually done in sulfate or chloride media; while solvent extraction has been used in different extractants: two-stage solvent extraction by D2EHPA and Cyanex 272 [6]. Solvent extraction of Cd from leach solutions has been studied using various extractants; Cyanex 301 [1], D2EHPA [7], Cyanex 302 [8], Cyanex 923 [9], Cyanex 272, Tops 99, PC88A [10]. Application of phosphorus based extractants for the solvent extraction studies of Ni such as TOPS 99 [11], D2EHPA [12], Cyanex 272 [2], has been investigated. Separation of Cd(ll), Ni(II), and Co(ll) from chloride leach liquor of spent batteries [13], were explored in the earlier studies. Cd extraction with D2EHPA involves co-extraction of both Ni and Co [14], which causes issues in the separation process efficiency."

Jan 1, 2012

By Derek Fray

Molten salts have been used for the extraction of metals since the 19th century but, recently, many interesting processes have been investigated using mixtures of molten salts and different cathodic materials. In several existing processes, the cation is simply discharged from melt but, in some cases, complications arise when the electrode potentials of the cations are relatively close. For example, the co-deposition of sodium with aluminium in the Hall-Heroult process is discussed in terms of electrode potentials of the components in the molten electrolyte. Similar considerations will also be given to the anodic reactions with respect to chlorine, oxygen, carbon dioxide or monoxide evolution from chloride-oxide melts. In some cases, the cathodic product interacts with the cathode to produce new and exciting products such as nanotubes from carbon or titanates and reduced titanium oxides from titanium dioxide. Depending on the electrode potentials, it is also possible to completely change the cathodic reaction from discharge of the cation in the salt to ionisation of the anions in the cathode. Examples are given of the reduction of metal oxides to produce metals, high technology alloys and nanomaterials and the cathodic refining of liquid metals.

Jan 1, 2006

By Sasa Djokic

In developed countries, the difference between demanded and produced quantities of non-ferrous and rare metals are compensated by secondary raw materials recycling and reprocessing of by-products from both ferrous and non-ferrous extractive metallurgy. Utilization of non-ferrous and rare metals from the metallic secondary raw materials is very significant, both for recovery of the metal value and contribution to the environment protection. Similar to all non-developed countries, the extractive metallurgy in Serbia was based on available natural resources and not so strict environment protection regulations, which was either insufficient or completely absent. Today, Serbia is at the beginning of development of efficient and economical technical and technological solutions in order to ?ecologize? technogenic systems by waste materials, secondary raw materials and degraded soils regeneration (by recycling and revitalization). Several metallurgical technogenic systems in Serbia, together with secondary raw materials classification according to their potentiality for metal extraction by using the existing technologies and expected economical and ecological effects of recycling, are discussed in this paper.

Jan 1, 2005

By Robert W. Hyers

Electromagnetic levitation has proven important in a wide range of experiments, all affected by fluid flow. For some experiments such as viscosity measurements, only whether the flow is laminar or turbulent must be established. For other experiments, however, quantitative assessments of velocity, shear stress, or shear strain rate are required. In most cases it is difficult or impossible to measure the internal flow in levitated droplets directly. The samples are usually small, opaque, reactive, high-temperature, metastable, or all of these. Furthermore, recirculating flow limits the utility of tracking surface particles, since they collect in stagnation points ratherthan following the flow. Most research groups have chosen mathematical modeling to assess the internal flow in levitated droplets. A variety of analytical and numerical methods have been applied, including both laminar flow and various turbulence models. A number of these models are reviewed and their impact on different containerless experiments is assessed. Much of the research reviewed here was performed by alumni of Professor Julian Szekely, and by others using similar methods.

Jan 1, 2006

By John A. S. Green, J. Gilbert Kaufman, Subodh K. Das

"The aluminum industry is a leading proponent of global sustainability and strongly advocates the use of recycled metal. As the North American primary aluminum industry continues to move offshore to other geographic areas, such as Iceland and the Middle East, where energy is more readily available at lower cost, the importance of the secondary (i.e., recycled metal) market in the U.S. will continue to increase. In the past, the recycling industry had been synonymous with the collection of aluminum beverage cans. However, as the opportunities for aluminum recycling have multiplied in motor vehicles, building and construction, and aerospace, these market are getting additional scrutiny for optimization of recycling strategies.Accordingly, the secondary industry can now draw upon a much wider range of product forms and alloys for its raw material, but this in turn brings issues of alloy sorting, impurity content, and control as the material is remelted and recycled into new product forms. The purpose of this paper is to take an integrated, industry-wide approach to look at the recovery of material from demolished buildings, shredded automobiles, and aging aircraft, as well as from traditional cans and other rigid containers. Attempts will be made to assess how the different alloys used in these separate markets can be recycled in the most energy efficient manner.IntroductionIn his recent book “Aluminum Recycling”[1], Mark Schlesinger points out that in traditional extractive metallurgy, the raw material used to produce a metal is mined from the earth and then is separated from other gangue minerals and impurities. In aluminum recycling, however, the ore body consists of scrap metal found on the ground, rather than in it. He further notes that scrap comes with its own variety of gangue and impurities such as painted coatings, other metal attachments, and even dirt and other contaminants. So, while the recycling process still requires some refinement and expenditure of energy, the effort and energy involved is much less than traditional mining."

Jan 1, 2008

By Y. Fukunaka, M. Niinae, E. Kusaka, T. Kuzuya, R. Ishii

"Samarium oxalattr particles was precipitated in oxalic acid aqueous solution from samarium-loaded D2EHPA solution emulsified with a conventional impeller. The calculated fractional precipitation of samarium oxalate was reasonably compared with the value determined by chemical analysis. Morphological variation of oxalate precipitate particles was then examined with H2C2O4 concentration in aqueous solution, Sm(III) and D2EHPA concentrations in organic phase. The needle-like precipitate was identified as Sm2(C2O4)3 10H2O by XRD. Precipitates obtained at higher H2C2O4· or Sm(III) concentration greatly decreased the length of major axis of precipitate, while those at higher D2EHPA concentration increased it. The oxalate was further precipitated under ultrasonic irradiation. However, the morphological variation caused by theses processing variables was not so evident under ultrasonic irradiation as in an impeller or shaking mixer.IntroductionThe materials processing of the rare earth elements must be reviewed from the scope of industrial ecology, since they have the potential applications of magnetic materials as well as secondary battery in developing programs of the electric vehicle. The technological trend to develop the electric vehicle may greatly influence the concept of materials processing, since the global· environmental problem must accommodate with the sustainable development for mankind. The recycle design must be a key issue in the materials science and engineering.Solvent extraction provides a unique separation technology -in this sense. Doyle (1)(2) reported the integrating solvent extraction with processing of advanced ceramic materials, whose chemical composition and microstructure must be precisely controlled. In her paper, the higher productivity inherent to the present process superior to hydrolyzing metal alkoxides was emphasized. Oxalic acid has been used as precipitant for rare earth purification process, since rare earth oxalate has a very small solubility in water and can be easily decomposed to oxide. It is thus suitable for precipitation stripping agent in cationic exchange type extracting system (i.e. D2EHPA, VA-10, PC-88A and so on)."

Jan 1, 2000

By Michael J. Nicol

Growing environmental and occupational safety concerns about the use of cyanide in gold processing has increased the interest in more acceptable alternatives. The most likely of these is thiosulfate. However, the thiosulfate process lacks a proven in-pulp method of recovering the dissolved gold, because activated carbon is not effective for the absorption of the gold thiosulfate complex .. Anion exchange resins do offer a possible route for in-pulp recovery. This paper describes work aimed at the evaluation of the effectiveness of commercially available anion exchange resins for the recovery of gold from thiosulfate leach liquors? and pulps. It has been found that strong-base resins are superior to weak-base resins in that they have a larger capacity, which assists in reducing the competition from other anions within a leach solution. Further studies with a selected commercial strong-base resin have shown that competing polythionateanions (particularly tri-and tetrathionate). Lower the maximum possible gold loading but that gold is selectively recovered over other base metal anions in solution. Kinetic experiments found that while? competilig anibns did not affect the initial rate? of gold loading it was important to minimise the contact time of the resin in solution so to prevent displacement of loaded gold by competing anions over longer times. A small-scale resin-in-pulp plant investigation showed gold can be recovered from a leach pulp by a strong-base resin to yield gold loadings of 3000 mg/L, barren pulp containing less than 0.05 mg/L of dissolved gold and. copper loadings of 500 mg/L. Loaded copper was displaced gold and at a loading of 2000 mg/L gold the copper loading was minimal «500 mg/L). The resin was found to recover gold adsorbed on the solids that would, otherwise have. reported to tails if a solid/liquid separation method were used. A patented two-step elution process in which copper and then gold are separately eluted from the resin is also discussed.

Jan 1, 1998