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By Denise Corrêa de Oliveira

Household zinc based batteries, dry and alkaline, has become the most popular sources of electrical energy, and are widely used. Because of their heavy metals content such as mercury, zinc and manganese, spent batteries cannot be directly placed in common landfills without a pretreatment. As a municipal solid waste, these batteries may cause serious health problems and environmental impacts. These damages can be reduced by recovery (which means saving natural sources and energy), recycling and adoption of cleaner technologies. Although this worry has been increasing recently, and producers are doing efforts to reduce the mercury content, batteries still need proper safe disposal conditions or recycling processes. This work presents the efforts in progress to characterize and recycle mixed - dry and alkaline - spent batteries, by using low cost unit operations. Some possible recycling stages and recovery parameters of metals as zinc and manganese are also discussed.

Jan 1, 2001

By Susumu Nagae, Hajime Ikeda

Recently, a number of mine development projects have been setback by social, economic and, environmental circumstances that had not been seen before. Many of these problems do not always originate from direct mine pollution. Typical examples of these are· conflicts between the exploration company and the local residents, sudden objections just before the development is to begin, and unexpected tightening of environmental regulations. The common background to these problems is expanding global environmental awareness. This includes complex factors ·such as the expansion of exploration to remote regions, the brisk activities of environmental NGOs, the increase of international environmental laws and, governmental policy changes. Today, the range of issues concerning mine development is widening significantly. The participation of local residents arid NGOs in the development planning, together with the company and government, has become essential for smoothly carrying out mine projects and making them more beneficial for stakeholders. Introduction The common image of the environmental problem with respect to mining is direct mine pollution, such as the collapse of tailings dams, pollution from refineries, and acid mine drainage. All over the world, the mining industry has made large investments in capital and technology to solve and prevent mine pollution, and these efforts have been making steady achievements. However in recent years, new cypes of environmental problems which are not originating directly from mine pollution are emerging frequently. Most of the problems are concentrated at the exploration stage to early stage of development, which have less impact on the environment. In the worst case, mining project may be forced to cancel and could cause serious damage to the industry because they could not collect their investment. I would like to take a general view of the examples of new types of trouble, their characters, background, and strategies against these problems.

Jan 1, 2000

By Youn-Bae Kang

Evaporation mechanism of S from liquid Fe–C–S alloys at 1873 K was proposed by analyzing available experimental data. It has been known that increasing C content in liquid alloy increases activity coefficient of S ðfSÞ, and it could raise driving force for the evaporation reaction S = S(g). However, experimental data of the evaporation of S in the Fe–C–S alloys could not be accounted for only by considering the increases of fS. In the present study, formation of carbosulfides, CS(g) and CS2(g), was additionally taken into account in order to explain role of C for the accelerated S evaporation. Surface adsorption of S was also taken into account, which retards the evaporation rate of S. An evaporation model equation was formulated. It can be applied to calculate the evaporation rate of S over wider C content (from zero to its saturation to liquid alloy).

By Mitchell L. Spencer, Viswanathan Panchanathan

"Bonded magnets are important category in permanent magnets. They are made by one of the following processes: compression bonding, injection molding, extrusion, calendering. An overview of the various bonded magnet processes and properties of products made with different magnet materials along with their applications are discussed. The main emphasis will be on the use of bonded NdFeB and ferrite magnets.IntroductionBonded magnets are a major growth area in permanent magnets. Bonded magnets are made by any one of the following processes: Compression bonding; Injection Molding; Extrusion and Calendering [1,2]. Compression and injection molded magnets are rigid magnets. Materials used in calendering process produce flexible magnets. Only the extrusion process makes both rigid and flexible magnets. The binders used for the bonded magnets vary depending on the processes. Thermoset, thermo-plastic and elastomeric binders are respectively used in compression, injection and the calendering process. Extrusion molding uses elastomers or thermo-plastic materials. The most co=on magnetic materials, Ferrite, SmCo, Alnico and NdFeB can be used in any of the above processes either alone or in combination as hybrid magnets. Another material that has been developed for co=ercial application is SmFeN. Making the material has been challenging and it is being used in niche market applications in limited quantitiesIn the extrusion process, a highly loaded compound is used to produce strip or sheet and is continuously extruded through a die. In calendering the granulated compound is rolled to produce a continuous wide sheet. In the compression bonding process a uniaxial pressing force is used. These magnets have higher loading compared to injection molded magnets. In injection molding the material is forced into a mold cavity and has lower loading compared to compression molded magnets [2,3]. Most of the flexible magnets are made using extrusion and calendering processes and the most co=on magnet material is inexpensive ferrite. Flexible magnets have been made using rare earth materials, but on a very limited basis.The major advantages of magnets processed by extrusion and calendering are as follows: inexpensive tooling, automation; practically any 2D geometry; fast production rates; no chipping or breaking; a wide range of properties; on-line magnetization; easy to convert (e.g. cut, punch or shape).Compression bonded magnets are inexpensive to manufacture. They have higher magnetic properties compared to injection molded magnets; however lower than their sintered counterparts. The magnet shape is restricted to simple geometries and they require careful handling. Their isotropic nature allows complex magnetizing patterns."

Jan 1, 2013

By Jay R. Hitchings

A technique that enables excellent color photograph production from black and white negatives of electron microprobe x-ray images is described in this paper. The photographs are made by superimposing one, two or three negatives of black and white x-ray images individually through assigned primary color filters directly onto color print paper. When used to examine metallurgical or geological microstructures, the resulting color photograph provides detailed, qualitative information about spatial arrangements, elemental associations and relative concentrations of at least three elements. The technique is simple and straightforward, requiring only standard darkroom equipment. The use of color to display or present complicated microprobe data also allows a non-technical reader or audience to better understand the data.

Jan 1, 1981

By Nobuyuki Higashiyama, Ikuo Yonezu

"Hydrogen-absorbing alloys containing rare-earth elements are used in high capacity nickel-metal hydride secondary batteries,' hydrogen storage systems for portable fuel cells, and refrigeration systems. New hydrogen-absorbing alloys containing rare-earth elements have also been developed and introduced into these applications. High performance in nickel-metal hydride secondary batteries is strongly demanded because of the remarkable advancements in portable electric appliances. A large hydrogen absorption capacity, high electrochemical reactivity and superior corrosion resistance in an alkaline solution are required for hydrogen-absorbing alloys used in nickel-metal hydride batteries. The aim of this investigation is to improve the performance of conventional LaNi5 type hydrogen-absorbing alloys. For example, Mm(Ni-Co-Al-Mn)„ type hydrogen-absorbing alloys with various non-stoichiometric compositions were developed. In addition, a new process of rapid quenching process was applied for preparing these hydrogen-absorbing alloys in order to improve their performance.IntroductionRecently, the trend in electronic appliances toward portability has increased the demand for high capacity of secondary batteries as power sources. Since nickel-metal hydride batteries were first commercialized in 1990 in Japan, they have become increasingly popular as power sources for cellular phones, portable computers, electric shavers, and other, products.The performance of a nickel-metal hydride battery, such as its discharge capacity, high rate capability, and charge-discharge cycle life, strongly depends on the characteristics of the hydrogen-absorbing alloy negative electrode. Many types of hydrogen-absorbing alloys have been developed so far. For a hydrogen absorbing alloy to be used as the negative electrode material, (1) it must allow a large amount of hydrogen to be absorbed and desorbed in an alkaline solution, (2) its reaction rate should be high, and. (3) it must have long term durability under repeated charge-discharge cycling. However, LaNi5, a typical rare earth-nickel type alloy, shows significant capacity deterioration during repeated charge-discharge cycling. Therefore the first step in its development was to obtain sufficient corrosion resistance of the LaNi5 alloy for its use as an electrode material. A partial replacement of nickel with cobalt and a substitution of the lanthanum- content with misch metal (Mm), a mixture of rare earth elements such as lanthanum, cerium, praseodymium and neodymium, were very useful in improving the charge-discharge cycle life. However, the discharge capacity of the alloy was still not sufficient for a practical battery. A study of the effect of the partial substitution of aluminum and manganese showed that the best alloy composition was Mm(Ni-Co-Al-Mn)x, as follows.The stoichiometry x of Mm(Ni-Co-Al-Mn)x largely affects the discharge capacity and cycle life. Theose alloys with non-stoichiometric alloys with the compositions of [Mm(Ni-Co-AMn)x: 4.7<x<4.8] have a large capacity and a long cycle life. Nogami' et al. reported that 'a non-stoichiometric alloy with a Mm(Ni-Co-Al-Mn)x (x=4.76) composition showed approximately 10% higher discharge capacity than the stoichiometric alloy (x=5) [1] and greater influence of x on the electrochemical properties of multi-component AB„ type hydrogen-absorbing alloys for batteries."

Jan 1, 2000

By Mingming Zhang, Udaya Bhaskar Kodukula, Marcelo Andrade

The physical and chemical properties of sinter feed are important factors that determine the productivity and quality of sinter product. In this study the feasibility of treating sinter feed by high pressure grinding rolls (HPGR) is investigated for selective cracks generation exploiting weak zones along grain boundaries of poor quality iron ores without generating much fines. The pre-treated sinter feed was characterized for size distribution, surface area, contact angle, and SEM analyses. The characterization results indicated that surface area of the pre-treated sinter feed sample increased about 20%. Pot-grate sintering tests results also indicated improvement on cold permeability, sintering yield and productivity, sinter Tumbler index, and low temperature degradation index (LTD) after HPGR pre-treatment.

Mar 1, 2018

By H. Kamiya, H. Hasegawa, M. Nojiri, S. Matsui, Y. Fukuda, M. Tsukada

"The present paper focuses on the action mechanism of anionic polymer dispersants in dense Si3N4 and SiC suspension. An atomic force microscope (AFM) was used to determine the relationship between the macroscopic suspension viscosity and the microscopic adsorbed structure of a polymer dispersant at the solid / liquid interface. The surface interactions within the suspensions were analyzed in various dispersant pH and additive conditions. The addition of an anionic polymer dispersant decreased Si3N4 and SiC suspension viscosity and increased electro-steric repulsion force on the non-oxide surface in solution at pH> 6 which was the isoelectric point of the materials. It was assumed that the increase of repulsive force was promoted by a hydrophobic adsorption of polymer dispersant on the non-oxide particles.IntroductionThe surface of silicon nitride and silicon carbide powders in a water suspension system has quite a complex molecular structure. In the case of Si3N4, hydroxyl and ammonium groups form on the surface and the pH of the suspension is increased from neutral to about 10 due to surface oxidation. The particle surface is negatively charged in alkaline solutions (pH=10), because the isoelectric point of silicon nitride exists in the pH range from 5 to 6. However, in spite of charging the negative surface charge, an anionic polymeric dispersant is generally used for the reduction in slurry viscosity.In dense SiC suspensions, an anionic polymer dispersant is generally used in order to disperse aggregates and reduce the suspension viscosity, too. Since an anionic dispersant is used in alkaline solutions higher than the isoelectric point of silicon carbide, the dispersant adsorbed on the negative charged surfaces of SiC.Few researchers have discussed and estimated the adsorption mechanism and structure of anionic polymeric dispersants on silicon nitride and silicon carbide surfaces. This is because it is difficult to observe the structure and measure the interaction at the solid/liquid interfuce directly. However, new developments in surface-force measurement technology have enabled the determination of non-DLVO type interaction for analyzing aggregation behavior2. The use of the AFM for analyzing the effects of various surfactants and co-polymers on colloidal dispersions and solid surfaces has also begun to rapidly expand to characterize the interaction between solid surfaces."

Jan 1, 2000

By J. M. Brupbacher, D. C. Nagle

"The XD TM * approach to producing metal matrix composites employs an in-situ precipitation technique for the formation of the reinforcement directly in the matrix of interest. Key features include: thermodynamically stable reinforcement; clean particle/matrix interfaces, single-crystal reinforcement; size, chemistry, and shape control; uniform distribution; compatibility with conventional ingot techniques; and grain refinement.Using XD~ technology it is possible to simultaneously introduce a number of different reinforcements in a given matrix, thus allowing for designing the microstructure to meet a specific material need. Thus, XD1l'1 technology is a very useful technique for achieving ""designer"" or ""engineered"" microstructures. XD TM technology has been applied to a number of systems including AI, NiAI, TiAI and Cu. Materials property and processing benefits will be discussed."

Jan 1, 1988

By Ma Keyi, Yang Xianwan, Zhu Xiaoyun, Guo Zhongcheng, Zheng Yanping

"The oxidation of the Multifunctional Electrodeposited RE-Ni-WP- SiC Composites at high temperature is investigated. The results show that during high temperature oxidation the relationship between the mass change of pure Ni , Ni-W-P, Ni-W-P-SiC or RE-Ni-W-P-SiC coating and the oxidation time follows a mixed curve, i.e. it is approximately a linear relationship when the oxidation time is less than 60 mins while it is a power function relationship when the oxidation time is over 60 mins. The order for the oxidation rate of the four coatings is Ni> Ni-W-P> Ni-WP- SiC>RE-Ni-W-P-SiC. The mass change of Ni-W-P, Ni-W-PSiC or RE-Ni-W-P-SiC coating increases exponentially with a rise of oxidation temperature. The high temperature-oxidation resistance of RE-Ni-W-P-SiC composite coating is 3-4 times that ofNi-W-P alloy coating. The cross section morphologies and Xray diffraction patterns indicate that the high temperature oxidation resistance of RE-Ni-W-P-SiC composite coating is better than any other coatings.1. IntroductionWith the rapid development of modem industries the products in engineering industry are continually challenged by the requirements of long-term and stable working at higher temperature, pressure, speed and under adverse conditions. Consequently, the surface properties of the products, such as the resistance to oxidation at high temperature, the resistance to wear and the resistance to corrosion, should be improved continually."

Jan 1, 2000

By F. Sakurai

The enlarged Mitsubishi process in Naoshima has been in steady operation since. May 1991. However, the sulfuric acid plants have been in operation for more than 30 years. The acid plants were modernized between 1999 and 2001 by renewing some of main equipment such as the drying tower and gas heat exchangers, and introducing new technology. At the same time, as an electric energy saving measure, the electric power consumption in the sulfuric acid plant was vastly improved by decreasing the volume of gas treated the installation of low temperature activity catalyst in the 1st pass of the converter and optimization of main gas blower runner. Furthermore, last year, the oxygen plant was replaced and enlarged, and anode production increased from 240,000 to 280,000 tonnes per year with an associated increase of sulfuric acid from 550,000 to 660,000 tonnes per year. This paper describes these recent improvements in the acid plant at Naoshima smelter.

Jan 1, 2002

By D. Morin

A general study of gold refractory arsenopyrite-pyrite concentrate bioleaching has been carried out including two continuous bioleach testworks at different sizes, namely one at a laboratory scale with a 100 I unit at a 2 kg/d dry solid flowrate and the other at a pilot scale at a 100 kg/d dry solid flowrate. Both tests show a 80% bioleaching of arsenopyrite in about four days of treatment and with the same kinetic. Pyrrhotite is attacked at the earlier stage of the bioleaching but pyrite remains unaffected. The weak potential of oxidation associated with the decomposition of arsenopyrite and the abundance of arsenite leads to a high grade of elemental sulfur in the bioresidue which consumes the major part of the cyanide during the gold recovery. Furthermore. the arsenite and ferrous produced in solution have to be oxidized to obtain a stable precipitate in the waste products and as outlined in previous works of other authors on this subject the addition of iron to obtain a Fe/As molar ratio at least above 3 is necessary. The agitation equipment used in the pilot unit allowed an optimization study calculation for scaling-up the design and power requirements of an industrial installation. For the pretreatment of a gold refractory As high-graded concentrate the reagent cost has the greatest part in the operating cost of the biooxidation step due to the necessary retreatment of the biosolution. In that conditions the power cost is quite marginal. actually it is significant for the treatment of pure pyrite.

Jan 1, 1991

By Thomas Schuman, Jaan Kers, Lucas N. W. Damoah, Xiangjun Zuo, Lifeng Zhang

"Rapid technological innovation has propelled the use of electronic equipment leading to the generation of more and more waste electrical and electronic equipments (WEEE). Printed wiring board (PWB) is a component made of one or more layers of insulating material with electrical conductors. To investigate an environmentally friendly process to recycle PWBs, PWB samples with and without additives were pyrolyzed. Liquid, gas and solid products were achieved with different conversion fraction. Analysis of the exhaust gases from the experiments using GC-MS and MS showed that without CaCO3 additives poisonous gases such as C6H6 and HBr were produced which were adequately controlled if CaCO3 was added.IntroductionPyrolysis is one of the best methods for treating complex mixtures of waste polymers and to recover the material and energy content. The process consists of thermal decomposition at moderate temperatures in total absence or small amount of oxygen in which the structures of polymers break down into smaller intermediate products "". The decomposition temperature of a substance is the temperature at which the substance breaks up into smaller substances or into its constituent atoms 2). Thermal treatment of PWBs were reported using DC Arc Plasma furnace 3), and fixed bed reactor 4). One drawback in dealing with thermal treatment of PWB scraps is the likely production of super-toxic halogenated dibenzodioxins and dibenzofurans from the bromine containing structures. Pyrolysis of organic materials contained in waste PWBs leads to the formation of gases, oils, and chars which can be used as chemical feedstock or fuels ""'. Dehalogenation of the pyrolysis product of electronic scraps is essential to make it commercially acceptable. It would be obviously the most advantageous solution as pyrolysis and dehalogenation are carried out simultaneously. Reported pyrolysis investigations are at experimental stage and have been carried out in vacuum, molten salt, fluidized bed, rotary kiln, entrained, stationary, and moving bed reactors 7). Comparing to the incineration and combustion of PWBs, the pyrolysis process has several characteristics: 8'"">) 1). Converting the organic solid substance into fuel gas, fuel oil and carbon-black as storage energy; 2) Emitting toxic substances such as sulfur, bromine and heavy metals in wastes; and 3) Keeping metals from being oxidized. Although many researches into the pyrolysis of PWB wastes have been reported, most of the works have been carried out using analytical pyrolysis techniques or very small batch reactors ""~'5). Also, most of the works for the pyrolysis of PWBs haves concentrated on the composition of the organic products, particularly the brominated organics. The current study is to investigate the pyrolysis of PWB powders in a small TG-DTA scale and a 50-gram tube furnace scale."

Jan 1, 2011

By J. R. Parga

A shortage of landfill space and growing environmental concerns in Mexico are renewing interest in the recyclability of scrap from automobiles. This work describes a pyroumetallurgical process for the recovery of metallic lead from waste lead paste. Argentopyrite concentrate is commingled with lead paste residue and smelted in a fuming process thereby transferring the precious metals into lead bullion. The process consists of smelting lead paste and argentopyrite, sodium carbonate, and metallic iron at smelting temperatures of about 1100 T. The reaction products are slag and molten lead bullion enriched with precious metals. A major feature of this process is the removal of precious metals from the bullion by means of zinc, whereby a silver-zinc intermetallic compound is formed and floats out of the lead. The recoveries of precious metals are about 98%.

Jan 1, 1996

By P. Regan

Following the introduction of the Contilanod process over 10 years ago at Copper Range and IMI Refiners, significant changes and advances have been made to this pioneering anode production technique. A new radial flow metal feeding concept has been developed that allows a substantial increase in casting rates on the Hazelett® twin-belt caster. To cut the 45 mm thick continuous anode plate into shaped anodes at rates of 100 t/h or more, a filly moving hydraulic shear designed by Mannesmann Demag has replaced the slower speed plasma cutting torch. Details of the.new caster and shear are presented along with operating results from the new lines starting up in 1999 at the Gresik smelter/refinery in Indonesia and the completely revitalized Mansfelder Kupfer und Messing complex in Germany.

Jan 1, 1999

By O. Nakai

In the copper electrorefining process, the quality of the starting sheet is one of the basic factors for producing high quality copper cathodes. A highly automated and advanced facility for the production of copper starting sheets was constructed at the Toyo Copper Refinery in 1992, bringing various improvements into an automatic stripping system using stainless steel mother blanks. In 1998, the refinery expanded the tankhouse by another 128 commercial cells, and introduced 64 polymer concrete cells in a first stage conversion. As a result, the Toyo Copper Refinery now has the capacity to produce 103,200 t/y of cathode copper. Construction has led to great improvements in the materials handling facilities and computer associated short-circuit detection technology. This report summarizes the improvements made in the quality of the cathodes and in plant productivity.

Jan 1, 1999

By Florian Kongoli

The so-called "fayalite" slag, despite problems associated with it, is the most widely used slag in copper smelting processes. Thirty years ago, in order to overcomes some drawbacks of this slag a new "calcium ferrite" slag was proposed especially for continuous copper converting. Since both slags have strong and weak points depending on the field of their application about 8 years ago another new "ferrous calcium silicate" slag was proposed that is expected to solve the drawbacks of each slag. This new slag is defined as mainly consisting of FeOx, CaO and SiO2 as its main components but it can practically have several combinations of these constituents. In order to determine the best area of this slag for possible industrial application the quantification of phase relations is an important subject. In this paper the work carried out by the authors in quantifying through an original physical model the phase relations, liquidus surface, liquidus regions, behavior of solid phases and the effect of minor components is reviewed. Several special compositions of this slag have been identified and discussed for possible applications in the industrial practice.

Jan 1, 2006

By Katerina Kryst

Antimony and bismuth are two of the elements that need to be removed from copper electrolyte to ensure a trouble free operation as well as to maintain copper cathode purity. One method to control these impurities is the use of aminophosphonic ion exchange resins. Antimony is present as both Sb(III) and Sb (V). Sb(V) is very difficult to remove from these resins, requiring excess amounts of highly concentrated hydrochloric acid. In industry this affinity of Sb(V) for the resin causes a buildup of Sb(V) and degrading resin performance due to continual reduction of resin capacity. A new method for regeneration of aminophosphonic resins loaded with Sb(V) has been developed, which utilizes catalytic regeneration of the resin. Ion exchange can then be utilized for continual control of Sb and Bi in copper electrolyte.

By Shijie Wang

In pressure oxidation leaching of copper anode slimes, than 65% of the tellurium is m&apos; cxtraoted during decopperizing. About l0- 15% of the selenium is also dissolved simultane¬ously by severe leach conditions. Current operation for the treatment of the leachate is to constantly recirculate the leach solution through a bed of copper turnings. The tellurium and sele¬nium are precipitated from the leach liquor as copper telluride and copper selenide and sepa¬rated from the solution by filtration. In order to improve the reaction efficiency and reduce the process cost, viz, minimize the copper addition, cut retention time, and reduce the energy consumption; a chemical reducing agent is studied and the cementation process tested in the laboratory. In this paper, the test results are presented and the process chemistry is discussed.

Jan 1, 2003

By R. W. Hammack

Results for the treatment of a problematic mining wastewater using bacterial sulfate reduction (BSR) are presented. Specifically, a BSR pilot treatment plant (250 L per day) was used to treat Berkeley Pit simulant to discharge standards with the selective recovery of separate Cu- and Zn-sulfide concentrates. Concentrates recovered in these tests contained greater than 50 % of the target metal and met specifications for sale to existing smelters. The biological component of the treatment was found to be surprisingly robust. Scaling and solid/liquid separation problems were encountered but considered normal for sulfide treatment. For Berkeley Pit water, capital costs for BSR treatment was found to be comparable to high-density sludge lime treatment. The value received from the sale of recovered copper ands zinc concentrates paid for all the operating costs.

Jan 1, 1999