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By Patrick R. Taylor

This investigation studied the inflight calcination kinetics of nuclear waste simulant using a thermal plasma reactor. A series of experiments were performed to determine the conversion of insoluble aluminum compounds to the soluble compounds and the decomposition of complex organic and nitrite compounds present in the simulant waste. Thermodynamic calculations based on free energy minimization were performed to establish a theoretical basis for this investigation. A kinetic model to describe the conversion of gibsite to sodium aluminate has been proposed. The products of the calcination were characterized using XRD, Gas Chromatography, and chemical analysis by ICP. The results of this investigation indicated 85% gibsite conversion to sodium aluminate, 90% of nitrate decomposition, 52% TOC decomposition and 90% conversion of chromium to soluble compounds. A process is identified for inflight calcination of wastes. Key words: Plasma, waste, simulant, calcination

Jan 1, 1996

By S. Mattlgod

Self-assembled monolayers on mesoporous supports (SAMMS) have been developed for the removal of heavy metals and some transition metals. The thiol functional groups were assembled on the internal and external surfaces of mesoporous silica with a uniform pore size of about 55 A. The mesoporous supports provide high surface area (>900 m2/g) needed for high metal loading in chemical separation. Self-assembled monolayers of organic molecules bond to the ceramic substrate with prescribed densities, and with terminal functional groups for excellent molecular selectivity. The unique characteristics include: (1) High metal absorption capacity, up to 3.2 mmol/g of SAMMS. (2) Fast Hg-binding kinetics (reducing mercury concentration from 0.5 ppm to 0.5 ppb in less than 5 minutes). (3) High selectivity in the presence of a range of cations, anions, and organic species. (4) Applicability in both aqueous and non-aqueous solvents. (5) Flexibility in surface chemistry. The materials can be designed to adsorb heavy metals, transitional metals, and radionuclides. (6) Chemical stability, and potential for regeneration or waste storage. This paper discusses the results on mercury adsorption.

Jan 1, 1999

By G. H. Khoe

Although some hydrometallurgical process liquors contain significant amounts of ferrous and arsenate ions, no reliable thermochemical data for the aqueous complexes and the solubility of the ferrous arsenate precipitate are available. The complexation of iron(11) with arsenate has been investigated using the potentiomemc titration method. The results indicated that virtually no complexation of iron(@ with arsenate has been observed. This is in contrast to the significant complexing reported for iron(1n) with arsenate. The solubility product of the precipitate was calculated using the concentrations of appropriate arsenate species pertaining to the observed precipitation pH's. The fit of the observed precipitation points on the solubility curve of the computed stability diagram was used to assess the appropriateness of the equilibrium model.

Jan 1, 1991

By Junji Shibata

Zeolite synthesized from coal fly ash has many intelligent properties such as cation exchange, adsorption, catalyst and so on. The suitable use of the zeolite, however, is not established in an actual commercial scale yet. From the viewpoints of an effective usage of coal fly ash and the zeolite obtained from coal fly ash, we propose the new concept for environmentally friendly usage of zeolite, in which coal fly ash safely returns to the soil with growing plants and purifying wastewater. This method can make great contribution to recycle of coal fly ash, to purification of high nutritious water and to tree planting.

Jan 1, 2002

By Yongfeng Jia

Lime neutralization and co-precipitation of As(V) with iron(III) is the most widely used and most economical method for the removal of arsenic from mineral processing solutions and effluents. However, the arsenate fixation mechanism in the coprecipitated solids is not fully understood. It was suggested by various researchers to be a ferrihydrite precipitation process during which arsenate is removed by adsorption on ferrihydrite. In this study, XRD, EXAFS and microprobe were employed for the speciation of arsenic and the effect of various factors on arsenic solubility was also investigated. The results indicate that coprecipitation is a more complicated process than simple adsorption resulting in lower arsenic solubilities. Poorly crystalline ferric arsenate was observed for the first time to be present in the coprecipitated solids. In case of lime as base, there exists some type of Ca-Fe-arsenate association. A general term ?coprecipitate? is suggested to describe the precipitated arsenic-bearing solids instead of those widely used specific terms ?arsenical ferrihydrite? or ?arsenic-bearing ferrihydrite?.

Jan 1, 2005

By A. J. Schindler, F-P Sawyer, T. Logan, M. L. Shutey-McCann, R. M. Perry

"Test work on biooxidation pretreatment of low-grade refractory gold ores has been ongoing at Newmont Gold Company since 1988, including laboratory testing and pilot biooxidation heaps (360 to 23,000 tonne). Metallurgical results of the biooxidation process utilizing Thiobacillus ferrooxidans (T. ferrooxiddans) have culminated in the design, construction, and operation of a biooxidation demonstration facility. The facility has processed 708,000 tonnes of refractory ore, using a batched process with separate pads for biooxidation and ammonium thiosulfate gold extraction. Siliceous sulfidic refractory (SSR) and carbonaceous sulfidic refractory (CSR) ores are treated separately during biooxidation pretreatment unit operation. Following biooxidation, the ores are neutralization with lime and placed on oxide leach pads or stacked on the ammonium thiosulfate leach pad. Gold is leached with either cyanide for SSR ores or ammonium thiosulfate for preg-robbing CSR ores.This paper will only address the biooxidation pretreatment process of the SSR and CSR ores.AcknowledgmentsThe authors appreciate the cooperation and approval of Newmont Gold Company Carlin Operations management for its support and permission to publish this paper. The paper draws on efforts and assistance of the following people and several others which are to many to list who participated over the past five years in bringing this project to its fruition: Dr. James A. Brierley, Chief Microbiologist, Newmont Metallurgical Services; Dr. Rong-Yu Wan, Metallurgical Manager, Newmont Metallurgical Services."

Jan 1, 1997

By Richard Hollis

The Mount Isa copper smelter was expanded in 1998 to a capacity of over 250000 t/y anode copper. This tonnage will be produced from a single stream consisting of an Isasmelt smelting furnace, and four Peirce-Smith converters - one of which was installed as part of the expansion project. During the course of the expansion project Mount Isa Mines Limited (MIM) signed an agreement with WMC Fertilizers Ltd (WMCF) to supply sulphur containing smelter gases over the fence to a new sulphuric acid plant to be built by WMCF. This will result in a further increase in copper production by reducing the time when smelting is curtailed by Air Quality Control restrictions. As well as the need to modify the primary gas system to connect to the acid plant, the hoods and crossover ducts and their support structures on the original three converters required replacement, and secondary ventilation was also needed to improve converter aisle hygiene. Each of these areas was addressed by the project. Preliminary ideas for carrying out the modifications were found to have a serious impact on converter aisle operations, and would have led to a production loss of over 50000 tonnes of copper. Following benchmarking in other copper smelters, a suitable construction plan was developed and carried out to minimise this loss. This paper describes the methodology and construction plan adopted.

Jan 1, 1999

By Charles Zimmerman

The Genesis gold mine, owned and operated by Newmont Gold Co., is located in section 31, T36N, R50E within Eureka County, Nevada along the Carlin Trend of sediment-hosted disseminated gold deposits. Mining commenced in 1986 with present mineable and stockpiled reserves listed at 17,711,000 tons of ore averaging 0.073 opt Au, totalling 1.292 million ounces of gold. Ore is primarily hosted within Devonian calcareous siltstones that have been subjected to intensive argillization and silicification episodes. Additional mineralogic and geochemical features of the Genesis ores include enrichment in iron-oxides, kaolinite, arsenic and antimony; the ore zone is relatively depleted in carbonates and sulfides as a result of supergene and hypogene oxidation. Two major structural zones enhanced the permeability of the siltstones and served as the main hydrothermal conduits within the deposit. Prior to the main ore stage, the host rocks were subjected to metasomatic effects caused by emplacement of the Juro-Cretaceous Goldstrike granodiorite pluton and associated dikes and sills. Micron-size gold occurs in clays, micro-crystalline quartz, and in arsenical complexes. Non-oxidized carbonaceous and sulfidic ores and silica-locked ores result in variable preg-robbing and refractory responses during cyanide recovery. Selective mining and milling has resulted in the successful treatment of the Genesis orebody.

Jan 1, 1988

By Andreas H. Vassiliou

Organic materials are major constituents of the ore in several uranium deposits. Some of these deposits have been described as "urano-organic" because, the organic materials are believed to have provided the dominant control for the accumulation and deposition of uranium and are directly and intimately intermingled with the uranium. The nature of these urano-organic deposits has been problematic in terms of (a) the origin of the associated organic materials and (b) the specific form of' occurrence of uranium. The organic materials in urano-organic deposits have been genetically related to both coal and petroleum or their progenitors or deriva-tives. Analytical data presented here (infrared, chemical. D.T.A.) suggest that coaliferous materials or related plant derivatives represent the main source of the organic fractions in practically all major urano-organic ores analyzed from the Colorado Plateau and other areas. Recognition of the specific form of occurrence of uranium in urano-organic deposits has been problematic mainly because the uranium is usually in an extremely fine-grained and disseminated state in the organic matrix. Electron microprobe and X-ray diffraction analyses presented here show that fine-grained uranium minerals, specifically uraninite or coffinite. are disseminated in the organic matrix as the predominant form of uranium in most major deposits; however. the presence of true organo-uranium compounds is also suggested for some deposits.

Jan 1, 1981

By Terry C. Cheng

The Akita Hematite Process is currently the only hydrometallurgical iron removal process producing saleable iron by-products in the zinc industry. In this study, McGill University and Akita Zinc Co. have worked together into elucidating the basic precipitation chemistry of the process from the standpoints of hematite product quality and prevailing precipitation kinetics. This work determined that hematite is produced under the applied conditions (T = 195?200oC,PO2 = 103?414 kPa) directly without prior formation of basic ferric sulphate and transformation of the latter to hematite as thought originally. The rate-limiting step responsible for the long retention time (~180 min) was found to be either the re-dissolution of ferrous sulphate according to the batch reactor studies, or the slow hydrolysis of the remaining ferric sulphate according to the continuous reactor studies. Another interesting contrast between the batch and continuous reactor data was the degree of sulphur contamination (1.5 vs. 3.8%, respectively) and the specific surface area of the product (10 vs. 30 m2/g, respectively). These differences in addition to the co-precipitation of SO4-containing phases such as jarosites, alunite, and anhydrite were attributed to the significantly higher supersaturation level prevailing in the industrial continuous autoclaves that yields highly aggregated sub-micron hematite crystallites contaminated with chemisorbed sulphate ions.

Jan 1, 2003

By Wang Youlai

Sichuan province is the richest province for its waterpower resource in China, perfectly suited to develop a high consuming energy industry. Sichuan Aostar Group Company has two Aluminum smelters, Guangyuan Aostar smelter and Sichuan Aostar Smelter. The production capacity of Aostar Group was 240,000 tons in 2004. The construction scale of Sichuan Aostar Aluminum smelter is 250,000 tons per year. The first 168 GY-300KA pre-baked anode cells (125,000 tons/year) were put into production in 2003. This company has taken the lead in the use of the transfer gantry technology in China. Besides making the process of calibration the pot shell it has concentrated the efforts to construct cell lining elsewhere. This company also has taken the lead in China for using the EIRICH force mixing and cooling technology as well as in the world for the CP Company?s vertical ball mill technology that produces the pre-baked anodes. The carbon anode system completed its 190,000 tons/year production scale. This is the most advanced technology and the biggest scale pre-baking anode manufacture in China. Since the Sichuan Aostar 300KA cell was put into production, it runs normally and smoothly. Up to now the current efficiency is higher than 94% and the specific energy is only 13300kWh/T-Al.

Jan 1, 2006

By Józef Czernecki

The Polish copper concentrates are characterised by low content of sulphur and iron. At KGHM Polska Miedz S.A. two copper production technologies are in use. The shaft furnace process is used at the Legnica Copper Smelter and the Glogów I Copper Smelter. A single-stage direct to blister Outokumpu flash smelting process is used at the- Glogów II Copper Smelter. Melting copper concentrates in the shaft furnaces is carried out in a reducing atmosphere and the product obtained is a matte. Instead, a result of melting copper concentrates by an oxidising flash process blister copper of a quality similar to that of converter copper is obtained. The annual copper production at KGHM Polska Miedz S.A. exceeds 450,000 tons. Another important metal is silver produced from slimes from copper electrolysis (about 1000 t/y). Moreover, such metals as Pb, Ni, Se, As, Au and other precious metals, including Pt and Pd, are recovered from various semiproducts. This paper presents technological flow sheet of the copper production in plants using the shaft furnaces and in another plant in which a single-state flash process is applied. Characteristics of products, methods of their utilisation, main parameters of particular technological operations, and advantages and shortcomings of the solution applied are presented. There are also discussed: the natural environment protection as well as directions of the KGHM Polska Miedz S.A. plants modernisation.

Jan 1, 1999

By Zuoren Huang

The flowsheet of the hyd.rametallurgical zinc plant which is in use at Zhuzhou Smelters is described. The principal features of the process are fluid bed roasting, continuous calcine leaching, solution purification, zinc electrolysis, electrolyte cooling, and finally, the melting and casting of zinc forms. The Zhuzhou process for the flotation of silver from the leach residue collected on the Moor filters is described. The technical details of the process are outlined and the operating data are analyzed. The flotation facilities are described in detail and concentrate grades and recoveries are presented. The waelz process is used to concentrate In, Ge and Ga remaining in the leach residue after silver flotation. These elements subsequently are recovered by selective leaching in sulphuric acid, and details of this operation also are presented.

Jan 1, 1990

By Corby G. Anderson

For over a century, the Sunshine Mine in Idaho has been a major producer of silver. An estimated 335,000,000 troy ounces of silver has been mined. This has established the Sunshine Mine as the largest single source of silver in the world. Because the dominant silver containing mineral is tetrahedrite, a copper and antimony sulfide, normal metallurgical treatments to recover the precious metal are not practical. Thus, over the course of the company's history, novel, hydrometallurgical technologies have been developed on-site to handle complex, precious metal containing materials. Recently, the use of Sunshine technology has been extended to the recycle of secondary materials. As well, the use of Sunshine technology by other organizations for treatment of both primary and secondary feedstocks containing precious and base metals is an area of growing interest. This paper will provide an overview of Sunshine hydrometallurgical technologies including the applicability of Sunshine technology to the recycling of precious and base metals.

Jan 1, 1995

By Bo Zhou

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

Jan 1, 2003

By Kathryn Hindmarsh

The most common method for the concentration of cyanide in gold leach circuits is based on the titration of cyanide ions with silver ions. This can either be done manually as a titration with a visual end-point or by using one of several commercial cyanide analysers which are 'based on the same titration but use a potentiometric end point This method has 'its limitations in the case of some ores such as those containing high amounts of soluble copper and those that are treated at low (less than pH 9) pH values in that the titration results do not accurately reflect the concentration of cyanide which is available for the dissolution of gold. This paper will present the results of the development of a novel "active" cyanide analyser which is based on the rate, of the reaction between gold colloids and cyanide. Gold colloids have a deep red colour and can be very simply prepared and stored for extended periods of time when stabilized. t has been shown that colloidal gold behaves similarly to metallic gold, dissolving in aerated sodium cyanide solutions to give the colourless Au(CNh-ion, This allows the reaction between the colloids and cyanide to be monitored spectrophotometrically at 520 nm. An automated instrument has been developed around this concept which can analyse a filtered pulp stream every few minutes with periodic calibration using standard cyanide solutions, Results of test work on synthetic solutions and solutions derived from several Australian gold plants will be presented as will the results of a comparative evaluation with a commercial titration analyser on a local gold plant

Jan 1, 1998

By S. C. Dhara

The recovery of Platinum Group Elements from various industrial scraps and spent materials in the form of high and low grade, such as, impure metals, matte, catalysts and other ceramic substrates, etc., has .been described by using high pressure reaction method. Nickel, Stainless Steel, Titanium and glass lined reaction vessels? are used in the reaction process. Primarily, the method involves either direct leaching of the substrates from the metal value or dissolving the precious metal from the substrate. Both acids and alkalies are used along with other reagents in the reaction process. The temperature and pressure of the leaching process are the main criteria for the reaction kinetics.

Jan 1, 1989

By John Wallace

"Monitoring compound semiconductor crystal growth using multifrequency eddy currents for sensing illustrates some of the extreme problems of measurement and interpretation that are not often seen in metallic systems. Using sensor arrays and scanning sensors have produced a qualitative and quantitative understanding of some of the high temperature electrical conductivity mechanisms in several compound systems. A detailed review of the CdTe/CdZnTe data is presented showing some of the complexity in the data as opposed to what is found in elemental semiconductors.HistoryThe most common goal in the use of eddy current measurement in crystal growth is to deter-mine the curvature of the liquid solid interface during growth to test if the heat transfer estimates of the thermal design were adequate for single crystal growth[l]. This aim could be met but represented only a small fraction of the data that was produced observing a growth cycle. A secondary consideration was what could be discovered in the recorded data about the growth and subsequent heat treatment as the boule cooled. This is usually a more difficult task because a crystal growth process is not a controlled experiment so much as a process that continually sees modification. Using a sensor arrays or a scanning loop has produced a qualitative and quantitative basis for understanding some of the high temperature electrical conductivity mechanisms. The implication of the these measurements of electrical conductivity variations are important in that they reflect the complex defect states that will occur on cooling and heat treatment following crystal growth. In contrast to the complex behavior of the conductivity of these compound semiconductors in the solid and liquid state we have the very well characterized system silicon to compare. Initially the interest on using eddy currents to monitor compound semiconductors came from G. Westphal at the Texas; Instruments Company in 1987 to monitor aspects of growth and compounding of GaAs. This was followed by work on solution growth of HgCdTe with D. Witter. The initial interest in the use of eddy cur-rents for monitoring CdTe crystal growth came from Prof. Wilcox at Clarkson University in the practical interest to determine and control the crystal interface curvature during vertical brigdeman growth. The first actual work was done by one of his former students. G. Neuge-bauer at the II-VI Corporation which was carried on by G. Rosen at Clarkson and R. Shetty at II-VI Corporation and with A. Socha at Johnson-Matthey Electronics. The work on CdTe extends over four years and yielded sufficient data to allow one to evaluate the utility of the information produced as compared to what could be obtained from monitoring an elemental semiconductor such as silicon."

Jan 1, 1997

By Atsushi Shibayama

The aim of this research was to develop a copper recovery process from mine tailings (0.34%Cu) using flotation followed by high-pressure oxidative leaching (HPOL) and solvent extraction. The results of HPOL using the concentrate of mine tailings obtained by flotation under the optimal conditions of the previous study shown that an efficient copper dissolution of 94.4% was achieved in an H2O media, while the copper concentration of PLS reached to be 2.9 g/L. The solvent extraction of PLS obtained from the optimal HPOL showed that 91.3% copper was recovered in stripped solution under the determined optimum conditions, in which the copper concentration achieved to be 44.8 g/L. Finally, a proposed copper recovery process from the concentrate of mine tailings was developed by combination of HPOL and solvent extraction, while a total copper recovery of 86% was achieved.

By Carla Lupi, Alessandro Pescetelli

"Spent lead battery recycling still shows few weak points in the achievement of a 100% recycling of different waste matters and by- products arising from the recycling process. Some of said problems are dealing with aqueous streams outgoing the recycling plant, and more particularly, a) the waste waters discarded from the breaking and separation unit, b) purification of the spent electrolyte drained from waste batteries and upgrade to a quality compatible with full re-use by the batteries’ manufacturers, c) purification of the mother liquors discarded in the sodium sulfate crystallization process so to produce a salt of commercial grade. All of the above listed problems have been satisfactorily overcome applying an electrochemical process that, through different process conditions and parameters, is able to remove the harmful impurities that hinder the successful commercialization of such by products, or, at least, that can avoid heavy and expensive treatment plant and operation.IntroductionAlmost 100% of commercial lead and lead alloys produced by secondary lead plants is recycled to the new lead accumulators manufacture. The other by-products and residues produced through the lead recycling process may be classified into two groups:a) matters reusable in the new accumulators production processb) matters produced as a result of various reagents and additives used in the recycling process, to be sold to different market sectorsQuality and saleability of by-products are significant points for the economics of the secondary lead plant operation, because, if said by-products are not saleable, they are just wastes, so offsetting potential revenues, and, at the same time, adding a heavy burden to operating cost, like disposal cost [1]. When looking at a typical, modern lead scrap batteries recovery cycle, it is quite evident that we are still rather far from dealing with a waste-less technology (fig.1).The group a) includes 3 by-products produced through the breaking process: among those matters the polypropylene only usually reaches a standard quality suitable for sale to lead manufacturing sector or to other sectors as well. The other two by-products, electrolyte and separators, do not still reach, through a viable and effective regeneration process, a quality standard sufficient for their re-use in the lead batteries sector ."

Jan 1, 2008