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By Feng Chen, Lirong Chen, Yufeng Guo, Wenjie Weng, Tao Jiang

"In this paper, the carbonthermal reduction behavior and the influencing factors of Panzhihua ilmenite under the condition of carbon-burdened were systematically investigated. The results show that the ilmenite forms into titanium nitride during the reduction process at 1200 °C under the condition of carbon-burdened. Carbon-burdened is beneficial to the reduction of iron oxide, but less favorable for the growth of iron grain.IntroductionThe titanium ferrous resources are very rich in Panzhihua-xichang area, accounting for about 38.85% of the world's proved reserves [1]. However, TiO2 grade of this kind of ilmenite is low and calcium magnesium content is high, it generally requires preconcentration to titanium-rich material—titanium slag or synthetic rutile.Chlorination process is an advanced method for production of titanium dioxide, which should takes high quality titanium-rich material with low content of calcium and magnesium as raw materials (the content of MgO and CaO are less than 1.0%). Ilmenite in Panxi area, however, contains high calcium and magnesium; it is not suitable as a raw material for chloride process. Methods of producing titanium-rich materials which have been applied in industry are electric smelting, various acid leaching and reduction rust [2-5]. There still exist some problems such as CaO and MgO removed not thoroughly, low resource utilization, high energy consumption and environmental pollution."

Jan 1, 2012

By Chang Wei, Fan Zhang, Zhigan Deng, Minting Li, Cunxiong Li, Gang Fan, Xingbin Li

Marmatite is an important resource of zinc, which exist in forms of high iron and high indium. In order to recycle the valuable metal from these ores, the testwork of simultaneous leaching on neutral residue mixed with zinc concentrate of high iron and high indium has been conducted. The primary objectives are to leach the zinc and indium remaining in the neutral leach residue as ferrite using acid, and to reduce the ferric iron in solution to the ferrous by zinc concentrate, thereby extracting the zinc and indium in the zinc concentrate. The results indicated that in the following conditions, mass ratio of neutral residue to zinc concentrate of 1:0.25, particle size of 74-58 μm, initial sulfuric acid concentration of 150 g/L, liquid to solid ratio of 8 L/kg, temperature of 90°C, reaction time of 4h, the leaching efficiency of zinc and indium were over 95%, nearly 90% Fe was Ferrous in the leaching solution. This process effectively extracted zinc and indium and converted Fe3+ into Fe2+ in solution, and simplified the traditional process of reduction after leaching.

Jan 1, 2016

By Ann M. Hagni

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

Jan 1, 1995

By Xue Ping

Sm2Fe17 alloy is an important precursor for the preparation of Sm2Fe17Nx magnet, which possesses a higher Curie temperature, larger anisotropy field, better resistance to oxidation and thermal stability. In this paper, the wet chemical co-precipitation was developed for synthesis of the Sm-Fe alloy oxide precursor. Based on the principles of simultaneous equilibrium and mass balance, a series of thermodynamic equilibrium equations of Sm(III)-Fe(II)-NH3-C2O4 2--H2O system at ambient temperature were deduced theoretically and the thermodynamic diagrams of lg[M2+]T (M=Sm, Fe) versus pH at different solution compositions were drawn. Then, the experiments were done to address the various effects on the wet chemical process, including solution pH value, reactant concentration, reaction temperature and aging time, etc. It is found that by precise control of the process, the Sm-Fe alloy oxide precursor was synthesized with fine crystallization and special size &size distribution.

Jan 1, 2008

By Christian Bernhard, Mario Hartl, Susanne K. Michelic

"One aspect of an efficient process and product optimization of the liquid steelmaking process is the understanding of reactions and interactions between the components steel, slag and nonmetallic inclusions. The present paper focuses on a fundamental study of this topic by combining the powerful methods of thermodynamic modeling with systematic experiments on a laboratory scale and subsequent SEM/EDS analyses. The modeling aspect is addressed by the commercial software FactSage 6.1; laboratory experiments are performed for a low-alloyed, Ca-treated carbon steel combined with varying slag compositions. The consequent SEM/EDS analyses provide a detailed insight into the inclusion landscape which offers a strong tool for characterizing the modification of inclusions. In the present study the combination of these methods is mainly applied to oxides, due to their crucial influence on the final product quality, thus giving important indications for further optimizing the secondary metallurgy processes.IntroductionIn recent years, the range of application for steels has been enlarged continuously; also resulting in extreme surrounding conditions combined with considerable stresses for the material. This trend is directly linked with higher demands on the properties of steels. In order to optimize the final product quality, the cleanness of steels is an important criterion. For this reason, the broad topic ""Steel Cleanness"" has become one of the main research points at the Chair of Metallurgy. Next to the continuous optimization of methods for the characterization of cleanness, the primary aim is to combine thermodynamic modeling and laboratory experiments in order to describe the changes in inclusion landscape under different conditions.The steel cleanness can particularly be influenced in the processes of secondary metallurgy. In different processes the reactions and interactions between the components steel, slag and nonmetallic inclusions (NMI) are essential for the final inclusion landscape. Consequently, the understanding of the occurring reactions is a fundamental aspect for further development and process optimization. In secondary metallurgy especially oxide-slag systems consisting of the components Ca0-Ah03-Mg0-Si02, which significantly influence the modification of NMI, are of importance. Several works dealing with the interactions of oxide non-metallic inclusions with different slag systems have been published in the last years [1-4]. In order to observe the dissolution of oxides in different slag compositions a Laser Scanning Electron Microscope is frequently used. A very detailed study on the ternary system Ah03-Ca0-Mg0 and its subsystems was also done by De Aza et al. [5, 6]."

Jan 1, 2011

By B. J. Scheiner

The presence of organic materials in gold ores interferes with gold extraction by cyanidation. The carbon contained in the ore has been shown to adsorb gold cyanide complex from solution. Removal of the carbon content by roasting or chemical oxidation prior to cyanidation results in gold extractions of 85 to 95%. This paper discusses how the mineralogy of the carbonaceous gold ores affects gold recovery by cyanidation. It also discusses the advantages and disadvantages of roasting and chemical treatment to render the ore amenable to cyanidation.

Jan 1, 1987

By Charles I. Richman

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

Jan 1, 1998

By John J. J. Chen, Barry J. Welch

"The production of primary aluminium can potentially lead to metal that, with minimum treatment, meets a high purity standard. Smelters that can achieve a significant proportion of their production in this manner have a competitive edge which is of growing importance as the use grows for such items as compact discs and the like. Superimposed on the desire to produce high quality metal are stringent environmental requirements that the industry must adhere to. The environmental legislation focuses on fluoride emissions and the approach adopted is towards a zero waste management philosophy. The fluoride recycling process does, however, result in volatile impurities being captured and recycled to the cell. Aluminium has an extremely high reduction potential and this results in a significant proportion of the recycled impurities being reduced at the electrolyte metal interface and thus contaminating the metal. This paper reviews sources of impurities and the impact of the operating procedures adopted on metal treatment.IntroductionSeveral factors have contributed to the immense growth in the aluminium smelting industry. Initially the ready availability of hydro electricity provided a primary reduction energy source for the production of the light-weight metal. Because of its unique properties and innovation in the industry there has been a continued exploitation of its unique properties, especially at the high purity end of the metal. The industry has shown considerably versatility and innovation in adapting to the ever increasing demands of quality and purity. It is however a competitive industry and the ability to produce high purity grade metal (>99.9% pure) gives a competitive edge. Emerging markets such as for CD ROM disc production etc, will keep the quality demand stringent.While the industry has met the continuing demands for metal quality, it has also had to respond to stringent environmental requirements for emissions from the production plant. Like all extractive metallurgical processes carbon dioxide is an inevitable reaction byproduct. However, the volatilization and hydrolysis of the solvent electrolyte leads to fluoride emissions that are potentially harmful. Accordingly, the industry has adopted essentially a zero non-process waste management approach. All cell emissions, including reducible impurities, are recycled back to the cell. This has had a significant influence on the metal treatment processes."

Jan 1, 1996

By J. Winters, L. Vos, C. Canoo

Committed to a sustainable development of zinc applications, Union Miniere is investigating processes for the minimisation of waste and residues originating from the classic hydrometallurgical zinc process. In that context, Union Miniere has developed a method for the cold inertisation and solidification of goethite, the Graveliet® process. The result is a hard and inert gravel that can be used in the building industry. During the past two years, a pilot plant for the production of Graveliet® has been built and operated. In the present paper, the Graveliet® process and the pilot plant are described after which the properties of the produced gravel are discussed, from both a mechanical and an environmental point-of-view. Graveliet fulfils the criteria for use as a secondary building material. The GravelietJ process is a viable technology to avoid stockpiling of goethite residues and it thus assures the long-term development of the hydrometallurgical zinc process.

Jan 1, 2000

Acid generation from reactive sulphide mineral tailings has become a major environmental problem in the mining industry. Initiation of chemical and biochemical oxidation reactions of the sulphide mineral leads to acid generation. A novel concept of safe disposal and utilization of reactive fine mill tailings is presented in this paper. The paper also presents the results of a preliminary laboratory experimental .study of the concept. The tailings are agglomerated using portland cement as a binder. The cold bonded agglomerates are encapsulated with other chemical additives to act as acid neutralizers, oxygen and ironoxidizing bactericides., The primary. factors influencing the choice of bacterfoides to inhibit the acid generating bacteria are their costs, toxicity and environmental friendliness. The paper discusses the utilization of agglomerated' products as aggregates for underground backfill, or as gravel for surface land cover.

Jan 1, 1991

By Petre Stelian Nita

In small steelmaking shops, in foundries and forging plants, there are not too many option to recycle the basic slags, which are not suitable for many purposes of recycling, because of their low chemical and structural stability. A solution of an adequate recycling is a direct recycling in EAF. Several quality requirements, physico-chemical properties and proportions of slags must be analysed. The progress in this fields permites to establish an adequate proportion of recycled slag, based on enough exact computation of the related property. For oxydizing slag, obtained during melting and in the first part of decarburization operation, the problem of phosphoms contents can be analysed using the phosphate capacity (C PO34-). For reducing periods, during deoxidization operation, desulphurization also occurs and the problem of the sulphur contents can be analysed using the sulphur and sulphide capacities ( Cs / Cs) Between this two complex thermodynamic indicators of the slags. a direct relation is established, using thermodynamic aspects, resulting from the equilibrium constants for dephosphorization and desulphurization process and also, using the optical basicity of slags, computable from the chemical analysis of the slags. On this basis starting from the steel quality requirements. adequate strategies can be established in order to obtain high rates of recycling (between 50-80%) of steelmaking slags. Important cost savings are obtained through this procedure, based on the correct amounts of the fresh lime, iron ore and fluidizers. Keywords: Slag, Properties, Recycling

Jan 1, 2003

By Klaus-Markus Peters, James G. Hemrick, John Damiano

"Work was performed by Oak Ridge National Laboratory (ORNL), in collaboration with industrial refractory manufacturers, refractory users, and academic institutions, to employ novel refractory systems and techniques to reduce energy consumption of molten material processing vessels found in industries such as aluminum, glass and pulp and paper. The energy savings strategies discussed are achieved through reduction of chemical reactions, elimination of mechanical degradation caused by the service environment, reduction of temperature limitations of materials, and elimination of costly installation and repair needs. Key results of several case studies resulting from US Department of Energy (DOE) funded research programs are discussed with emphasis on applicability of these results to high temperature processing industries.IntroductionRefractory materials are limited in their application by many factors including chemical reactions between the service environment and the refractory material, mechanical degradation of the refractory material by the service environment, temperature limitations on the use of a particular refractory material, and the inability to install or repair the refractory material in a cost effective manner or while the vessel is in service. All of these limitations reduce the energy efficiency of the process as degraded refractory materials lead to loss of process heat (reduced insulation by refractories) and the need for maintenance through repair or replacement of refractory linings.This situation is conceptualized in Figure 1 which shows that when the thickness of the refractory wall is reduced by chemical or mechanical degradation, the heat losses through the wall increase exponentially. The subsequent maintenance to repair such conditions often requires cooling of the furnace or refractory lined vessel which entails loss of energy due to cooling and consumption of energy due to reheating. Additionally, production time and capability are sacrificed.Additionally, in most applications where refractories are used (metal melting furnaces, glass furnaces, steel making furnaces, gasifiers, etc.) wear of the refractory lining is not uniform. Very often, specific areas will wear (become thinner) more rapidly due to exposure to more corrosive or erosive conditions. This concept is illustrated in Figure 2, through the example of excessive metal line corrosion."

Jan 1, 2009

By W. F. Whittaker

Systematic control of process parameters during electrorefined copper cathode production and final product inspection ensures high quality of produced "ORC brand copper. Since 1986, substantial increases in tankhouse productivity have been achieved by a number of technological and process control changes. This paper reviews the changes implemented to achieve higher productivity and cathode quality.

Jan 1, 1992

By William J. Mallio

Substantial differences between in situ and conventional technology require that in situ ore grade be established for deposit as distinct from the total contained metal value. Establishing an in situ ore grade involves determining the fraction' of the contained metal that can be leached by the fluid. This depends on the proportion of the ore minerals that occur on fluid flow paths as defined by the permeability distribution. Mechanisms involved in the in situ mining of sulfides are: oxidation of the sulfur, solution of the metals, complexing of the released metals, and a transport to a recovery point. Metal ions may be delayed or lost due to inefficiencies in these pro-cess steps or by reactions of the metal ions in solution with the rock. These reactions can involve precipitation of new phases, exchange of the metals of the interest with Ca or Na in clays or zeolites, retention of metals in oxidized mineral grains, or secondary enrichment of other sulfides along the paths of the solution flow. The efficiency of solution of metals and potential loss or delay mechanisms are controlled by local equilibria (the Eh, pH conditions) present in different parts of the ore zone. Permeability distribution in the rock mass and the coincidence of ore minerais with flow channels must be determined before a deposit can be judged suitable for in situ mining. Laboratory studies indicate that the natural permeability system is dependent on the degree of cementation of veins by late generation hydrothermal activities. The major conclusions of the study are:, 1. Deposit selection is critical; suitable deposit types include deep lying sedimentary deposits, selected zones of porphyry systems and vein controlled hydrothermal deposits; 2. Adequate laboratory and geochemical analyses should be undertaken through quantitative petrographic study and permeability mapping; and 3. Economic incentives for in situ mining must consider limitations of recovery caused by inefficiencies in dissolution and transport associated with particular deposits.

Jan 1, 1981

By Frank Mucciardi, Hujun Zhao, Pietro Navarra

"A heat pipe is a device having a very high effective thermal conductivity in which two-phase flow and heat transfer takes place. Recent research at McGill University has led to a new type of heat pipe that contains a flow modifier. This improvement has enabled the device to operate at the high heat fluxes encountered in the metallurgical industry.This paper summarizes the progress made to describe the fluid flow in the evaporator section of a McGill heat pipe with the goal of understanding how the flow modifier configuration is linked to the film boiling and dry-out limitations. A separated flow model, an instability analysis, a lift-off model and an energy balance model are used to calculate the theoretical CHF with varying flow modifier configurations and operation conditions. A summary of the current work to relate the flow modifier to the dry-out limitation is also given.Determining how the flow modifier affects both the film boiling and dry-out limitation will give insight into improving the flow modifier design so as to extend the operational range of McGill heat pipes in terms of maximum heat flux and heat load capabilities.IntroductionThe McGill heat pipe is a specialized two-phase heat exchanger developed for several metallurgical applications where temperatures and heat fluxes are typically close to or beyond the maximum safe range of conventional cooling technology.Over the last few years, several breakthroughs have brought this device beyond the proof-of concept stage and a series of industrial trials have been performed with success. These trials include two oxygen injection applications for the ferrous and non-ferrous industry [l], and two light metals permanent-mould casting applications [2,3]. Current projects include a blast furnace copper taphole cooling application [4], a copper smelting application and a thermal analysis probe application."

Jan 1, 2004

By Adam J. Gesing

The eddy current separator (ECS) is designed to separate nonmagnetic (nonferrous) electrically conducting (metallic) particles from nonconductive residue. Nonferrous metallic particles are repelled out of the material stream passing over the eddy current rotor (ECR). The rotor is housed in a fiberglass composite outer shell that serves as a conveyor head pulley. This results in the desired metaVnonmeta1 separation. The behavior of ferromagnetic particles, mainly iron and iron oxide (i.e. rust), is quite different. These particles are strongly attracted to the magnets and the smaller particles tend to align their long axis in the direction of the magnetic flux. Since the direction of the flux changes with the passage of each magnet pole, the small particles spin at very high rates causing wear of the belt and of the composite outer shell housing the ECR. Large particles, when trapped under the ECS belt, cannot spin, but can be heated by the eddy current effects and subsequently can burn through the composite outer shell. We discuss the practical implication of this behavior of iron and rust on the design, performance and maintenance of eddy current separators.

Jan 1, 1999

By K. Gao, R. Dry

"Carbon boil, which results in excessive spitting and even complete destruction of a metal drop, could significantly influence the efficiency of direct smelting processes. Carbon boil has been studied as a function of some key parameters such as melt sulfur content, oxygen partial pressure, and melt area/volume ratio. The time of carbon boil was determined using a CCO camera coupled with a time/date generator connected in parallel to a video recorder and a computer. The time of carbon boil was in the range ~5 - 15 seconds under the conditions in this study. A mechanism for carbon boil has been proposed.IntroductionThe occurrence of carbon boil in molten iron drops can result in excessive spitting and sometimes even complete destruction of a metal drop. In direct iron smelting processes, this could significantly influence the decarburisation of liquid metal and the post combustion and hence may influence the efficiency of smelting processes. The generation and consequent ejection of metal droplets into the gas phase occurs due to the intense turbulence in the bath which results from the injection of gases and coal. The aim of this investigation is to understand the fundamentals governing the carbon boil phenomenon under direct iron smelting conditions to assist control of process efficiency.Carbon boil phenomenon has been studied as a function of some key parameters such as melt sulfur content, oxygen partial pressure and melt area/volume ratio. The time for the occurrence of carbon boil has been determined in this study at 1440 °C using a novel approach which includes utilisation of a CCD camera coupled with a time/date generator connected in parallel to a video recorder and a computer. This arrangement permits the capture of the entire sequence of events leading up to carbon boil and therefore the determination of time of boil which is in the range -5 - 15 seconds under the conditions in this study."

Jan 1, 1996

By Xiaobing Yang, Animesh Jha, Greg Doughty

"Successful use of inert anodes should reduce the CO2 footprint in aluminum production. The search for a “holy grail” inert anode for metal electro-winning from constituent oxides using molten salt bath as an electrolytic medium is continuing. In this article we demonstrate the engineering approaches for the fabrication of intermetallic anodes, based on a quaternary Al-Ti-Cu-M (M:Ni, Fe) system for primary aluminium production. In particular, we examine the microstructural and electrochemical properties of alloys, based on the quaternary compositions. We explain the aspects of phase stability under anodic potential, which leads to the loss of anodic materials in the temperature range of 850-1050oC. The results are analysed in the context of oxidation reaction and formation of oxide layers which readily dissolve in the cryolite melt and prevent passivation. The paper also describes the conditions under which the reduction of aluminium at the graphite cathode occurs which also strongly depends on the molten salt chemistry for the nucleation of molten aluminium at the cathode.1. IntroductionOxygen-evolving inert anodes are an alternative to the conventional consumable carbon anodes for the production of primary aluminium. In this paper the materials selection criteria chosen for the engineering of anode is based on the understanding of the thermodynamic stabilities of aluminide intermetallic phases, some of which are formed and remained stable in fluoride melts. For example, the formation Al3Ti dispersed in aluminium metal via molten-fluoride flux reaction is well known in the context of aluminium casting and grain refining [1-3]. It is for this reason in our research we concentrated on the engineering of stable intermetallic phase mixture in the Al-Ti-Cu ternary system, shown in Figure 1 [4]. In this figure two compositions in the Al3-0.5zTi1-0.5zCuz family are shown with the substitution of 7 atomic % and 11 atomic % copper. However initial investigations showed that these two compositions were unsuitable due to the formation of low-temperature liquid (~540oC) and intermetallic phase, Al2Cu along the Al-Cu binary edge during solidification. The Al2Cu phase segregated along the boundaries of Al3Ti and Al5Ti2Cu, and dissolved away when electrolysis was carried out using these anodes above 800oC. The presence of consequential porosity in the anode material increased the corrosion of the alloy through local heating due to high current density at 0.8 A cm-2. The early tests were carried out with cryolite melts, shown in Figure 2, having 3 weight percent of Al2O3 in the bath at 850oC."

Jan 1, 2010

By Carl C. Nesbitt

A study was conducted to examine the treatment of metal-bearing effluents by precipitating the metals as sulfides and simultaneously collecting the particles by flotation. The precipitant was hydrogen sulfide gas which was introduced into a bench-scale column cell with air. The study included experiments of various flotation reagents and column configurations in treating solutions containing dissolved copper, lead, mercury, iron, zinc and cadmium. An acidic laboratory waste from a local copper operation was used to test the column with a solution containing several metals and arsenic. Precipitates were observed to form at the gas/liquid interface when the gas mixtures were rich in H2S. Copper, mercury, lead, and cadmium were precipitated from solution as sulfides to concentrations near detection limits. The flotation of these precipitates was enhanced with small amounts of S-7151 promoter from American Cyanamide Company and Dowfroth 1263 mixed with the feed. The recovery of the precipitates in this manner produced a smaller volume slurry which was easier to dewatering than a slurry produced by conventional precipitation techniques. The low pH and high oxidation-reduction potential in the cell from H2S addition was not conducive to form precipitates of iron, zinc or arsenic. However, these ions were precipitated as sulfides by raising the pH of the column discharge.

Jan 1, 1994

By K. Soldenhoff

The Bulong deposit, situated near Kalgoorlie in Western Australia and owned by Resolute Limited, is a lateritic deposit containing on average 1.1% nickel and 0.09% cobalt. A process has been developed and tested at the mini-plant scale for direct solvent extraction and separation of Co and Ni from solutions derived by acid pressure leaching of Bulong ore. In this paper, two solvent extraction processes are described. The first process uses Cyanex 272 to extract cobalt and reject nickel to the raffinate. The second process uses Versatic 10 to extract and purify nickel. The loaded strip nickel solution is suitable for electrowinning. Results of both batch laboratory tests and continuous mini-plant trials are presented. The selectivity of the solvents with respect to the major impurities such as Mn, Mg, Ca, and Zn is also discussed.

Jan 1, 1998