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By Emilia Visileanu, Eftalea Carpus

"The strategy of developing the Romanian textile industry sub-sectors envisages the achieving of certain superior production indices, from a physical and value point of view, in 2010, a quantitative increase of textile wastes by 14% in 2010 as compared to 2000, implicitly. The percentage of the turned-to-profit wastes will have an increasing tendency, from 53.6% in 2000 to 74.7% in 2010. The article synthetically presents the innovative elements of the technology of processing the industry textile wastes.1. Introduction“People will need to re-adopt this sense of rarity that has been forgotten over the last two centuries. Humans need to collect, sort, recover, going back to the old ideal of alchemists: complete the material cycle, turn waste into resource, reduce all forms of predatory behaviour as much as possible”Irrespective of the historical period, geographical positioning, economic power or employed technologies, wastes resulted and will result in a bigger or smaller quantity as long as life and activity on Earth go on. The negative effects of these over the environment factors and implicitly over population health are well known all over the world and not approaching this matter enough may have catastrophic consequences over life. Having in view these aspects, finding solutions for diminishing the general waste quantity and limiting the negative effects of those products is important, by effecting the reusing of the recyclable ones in the production processes as secondary raw materials, and by ecologically treating and storing those than cannot be reused.2. Experiments and researchesThe textile industry affects the environment by the high water, energy and chemical consumption, as well as by the high quantity of wastes that are the result of using an impressive number of chemical substances and technological processes.The development strategy of the Romanian textile industry sub-sectors foresees, for 2010, the achieving of certain higher production indices as compared to 2000, both in terms of materials (as merchandise) and in terms of value, which implicitly leads to a quantitative increase of wastes.The flexible, economic and ecologic technologies which include systems of waste preliminary preparing (cutting, opening) and conventional or non-conventional system of processing the recovered fibres lay at the basis of substantiating the activity of implementing the notion of zero wastes."

Jan 1, 2008

By Sergio Bustos

Covellite resulting from an original 0.5 % Cu(tot) chalcocite ore has been leached in columns at different temperatures, in the lower range of 10 - 20 °C, under acid - ferric bacterial leaching conditions. Dissolution of copper from covellite depends on the rate and extent of sulphide oxidation by ferric ion. While it is recognised that the dissolution of sulphide minerals is electrochemical in nature, an apparent chemically controlled dissolution pattern was measured with activation energy of 78.09 kJ/mol (18.66 kcal/mol). Ferric iron is the main oxidant and its production and availability will depend on the bacterial activity developed in the system. This activity is characterised by the population size and by the specific oxidation rate of the bacteria. Bacterial growth was followed directly by the number of bacteria appearing in the column effluent solutions and indirectly by the generation of ferric iron or by the total oxidation observed in the columns. These results have been interpreted by using the heap oxidative capacity parameter, which indicates an equivalent ferric production of about 0.07 - 0.15 kg Fe +3/t/day at 20°C. Although bacterial activity decreases to about 0.03 kg Fe +3/t/day with decreasing temperature, a significant bacterial oxidation is still observed at 10 °C. However, extended lag times are observed, which delay the start of bacterial growth to times concurring with covellite leaching. Under these conditions, bacterial activity is displayed through a population controlled by the rate at which- ferrous iron is released from the reducing covellite surface. These results suggest the potential benefit of including some kind of inoculation when operating at lower temperatures. Also, heat loss control and/or heat addition to the heaps should be considered during process design and operation of ferric bacterial heap leaching of secondary copper sulphide ores at temperatures lower than 20°C.

Jan 1, 1999

By Ju Shao-hua

Although nowadays gold extraction methods are very abundant, none of them is satisfying, especially, in the field of heap leaching of low grade gold ore. The traditional heap leaching method of cyanide method plays an inglorious role of badly environmental pollution. In this paper, a bran-new and innoxious method of gold extraction system, metal-ammonium-chloride-ammonia (MACA), was proposed, and also analyzed both thermodynamically and practically. Thermodynamically, according to the principles of simultaneous chemical equilibrium and electronic charge neutrality, the thermodynamics of Au-NH4Cl-NH3-H2O system was studied by using the exponential computation method and through MATLAB programming, and the solid figure of its potential - c(NH4Cl) - c(NH4OH) was drawn. The results showed when the concentrate of ammonia is higher than 0.6 mol?L-1, fAu+/Au is only about -0.2 v. Practically, the leaching results of a cuprous gold ore showed that the extraction of gold can reach to 80% in this system. The preliminary results of reduction of the rich solution with copper and zinc powders showed that with deoxygenizing, the reduction effects were relatively good. These new findings and results have established a theoretical and practical base for developing a new process for heap leaching of low grade gold ores in this system. And the new process owns a series of merits such as, non-cyanogens, nontoxic, broader applicability.

Jan 1, 2006

By Min Zhu, Yu Ji, An-chao Ren

"After being welded in the weld plant, the 100-meter heavy rails with the specification of 60kg/m are found broken during the straightening process in four planes. Failure analysis is made using the optical microscope and SEM with the result showing that the broken rail contains the imperfection of protrusion which exists at the edge of rail foot, about 1 00mm away from the rail end. When the protrusion is peeled off by deseamer from rail surface, cold scratch is generated which causes the rail to be broken during the subsequent straightening process. By adjusting the roll diameter differences between top and bottom roll of universal finishing mill and the height of pass line, it is possible to maintain the rails flat when leaving the mill. This prevents the upsweep and downsweep phenomena and, thus, the imperfection of protrusion can be eliminated. IntroductionThe development of rail transit worldwide has entered into a new era since the 1960s. The hi-tech rail transit system has gradually gained recognition over the world. In particular, the emergence of new-type passenger trains represented by TGV of France, ICE of Germany and Shinkansen of Japan and heavy haul trains as well, has revealed the charming way and more prosperous future of the modern and hi-tech rail transit system to the people all over the world. It should be pointed out that rail transit system is still the most effective solution to traffic jams among urban cities and in the central cities during the 21 '1 century, especially high-speed railway and subway which take overwhelming advantages over air transport, marine transport and road transport in terms of high speed, high efficiency, safety, comfort, environment protection and high flow. With the trend of increasing speed and heavier load of trains, higher product quality of rails is demanded. The rails for passenger dedicated lines require high cleanness, high accuracy in size, high flatness, high surface quality and large size (100-meter fixed length). The rail quality has direct influence on the operating performance of rail and railway traffic safety. The 100-meter heavy rails with the specification of 60kg/m are broken subject to the straightening process in four planes after being welded in the weld plant. This paper analyzes the reason for rails being broken and provides the theoretical proof for determining the rolling process."

Jan 1, 2013

By V. K. Handa

Sterlite Industries (I) Ltd. started its copper smelter in 1996 and worked through the common problems associated with smelter start-ups. Specific issues in the converter area included converter blower IGV problems, punching machine reliability, converter spitting, back collar burning, ,and short converter campaign life. With a very young and dedicated team of engineers and technicians, smelter management assigned teams of three to four members to work scientifically and systematically through each major problem area to recommend and implement appropriate solutions. The converter mouth was redesigned with respect to tuyere and metal height to eliminate spitting and back collar burning. The air line was changed in places to reduce the pressure drop. A new back-up compressed air line and vessel was installed to prevent tuyere blockage in the event of a blower trip or power failure. The converter mouth liners and bricking around the mouth was modified to eliminate metal leaking through the pouring lip Modifications to the punching machines were made to address specific problems and preventative maintenance practices were further streamlined and reinforced to ensure 100% availability of hot metal cranes, converter blowers, punching machines, and ID fans. Matte availability and matte temperatures were improved by streamlining the upstream ISA and Rotary Holding furnace areas. Implementation of a detailed training program for the converter operators significantly improved the operation and morale. Water-cooled double hoods and a third converter were installed as part of the smelter modernization plan. The new hoods dramatically improved hygiene in the crane aisle while the addition of the third converter posed new challenges for the same motivated group of crews with respect to flip flop operation to keep the idle converter hot and to maximize in-stack time, managing crane/ladle logistics, and managing revert generation. This paper describes the converter operation's journey from the initial days of long blowing times and large revert accumulations to present operations with two converter flip flop operation, and also describes the team work, constant focus on increasing productivity and reducing costs, and benchmarking.

Jan 1, 2002

By Padmavathy Mahadevan, Samir Chefai, Eduard Guerra

"Electrocoagulation is a technique for treating wastewater streams from metallurgical plants whereby electrodes are corroded to generate gases (most notably oxygen at the anode and hydrogen at the cathode) and solid particulates which acts as substrates for coprecipitation of impurities. The performance of electrocoagulation reactors, in terms of their efficiency for removing a particular impurity, is highly dependent on several factors, most notably: the nature of the electrodes, the spacing between electrodes, the current density, the height of the electrodes, the solution flow rate, and application of periodic current reversal. Because these variables have complex interactions, in order to ensure reliable scale-up of laboratory results, experiments should be conducted under conditions that closely match those that would be employed at an industrial scale. To that end, this article describes the design and commissioning of a versatile laboratory scale electrocoagulation reactor that allows for the control of all the aforementioned variables along with the ability to measure the instantaneous spatial distribution of current within the reactor.IntroductionArsenic is often removed from metallurgical waste streams in stirred tank reactors by coprecipitating it with ferric ions as an arsenical ferrihydrite [ 1]. Electrocoagulation is an electrolytic technology that can accomplish the same task, but has not yet been widely adopted to treat metallurgical waste streams [2]. The electrocoagulation process involves the use of an external DC power supply to drive the dissolution of a relatively non-toxic metal into the wastewater stream, usually either iron or aluminum, which then largely precipitates as oxyhydroxide phases that adsorb undesired impurities [l]. At the anode, the metal is dissolved and oxygen is often evolved, lowering the local pH and enhancing metal ion solubility."

Jan 1, 2012

By A. Filzwieser

The highest current density suitable for the electrowinning process is between 50 to 60 % of its limiting current density. One of the most important influences on the limiting current density is the thickness of the hydrodynamic boundary layer near the electrode surface. Therefore, the fluid flow in a copper electrowinning cell is calculated. The numerical simulation - using the CFD-software package FIRE® - considers all three different types of the fluid flow, namely, the natural convection, the forced convection by electrolyte circulation and the forced convection by electrochemically induced gas stirring. The simulation of natural convection is based on the different density values in the boundary layer at the electrode surface given by a density/concentration correlation. The copper concentration - linked with the current density by Faraday law - is solved by an additional transport equation. The simulation of the forced convection by the electrochemically-induced gas stirring is done by using a real two-phase calculation. That means that all differential equations are solved again for the second phase. The numerical solution of the fluid flow field is compared with the results of LDA- measurements, which were done in a special cell. The software for the LDA enabled a calculation of the void fraction possible and therefore a rough estimate of the mass transfer coefficient through the prevailing gas bubble induced convection can be made by assuming the influence of relative bubble volume.

Jan 1, 1999

By Aurelian Buzaianu, Cristian-Aurelian Popescu, Gabriela Popescu, Petru Moldovan

"A lot of scraps result in processing of composite materials which contain metallic phases that can be recovered and used again in different field. Considering this point of view the aim of the paper was to separate and recover aluminum from aluminum matrix/graphite composites. The separation and recovery of aluminum alloy from aluminum alloy/graphite composites was done by treatment with halide molten salts. As halide salts were used flux tablets that collect the ceramic particles in dross. After dross separation, was used filtration in order to separate the aluminum matrix from the other impurities.Samples from the recovered alloy were analyzed using chemical analysis, optical and electron microscopy, as well as X-ray diffraction. The desired composition of the aluminum alloy obtained from scraps could be reached by some addition of metals to the metallic phase. From optical microscopy it was obvious that the structure of the aluminum alloy obtained after composite reclamation consists large particle of silicon, eutectic, a-Al solid solution and other phases like Fe, Si, Mg and Ni, or some compounds like CuAl2. 1. IntroductionThe research on the recycling and reclamation of metal-matrix composites (MMCs) becomes active to preserve the natural environment, as environmental requirements become stricter, to save energy, and to reduce garbage. In case of recycled aluminum alloy ingot the production energy is about 3 pct of that of the new ingot. This evidence strongly supports the necessity to recycling of aluminum alloys. Among aluminum alloys, metal matrix composites have high strength and elastic modulus, and also good were resistance. These materials have been developed to meet the demand properties which exceeds that of the ordinary materials, and to save energy."

Jan 1, 2008

By C. A. Nogueira, F. Pedrosa, F. Margarido, R. N. G. Guerra

"A hydrometallurgical process for recycling spent Zn-MnO2 batteries was developed, involving leaching with sulfuric acid, purification by precipitation and metals separation for further recovery. Leaching of zinc oxide was easily attained while for manganese oxide was rather difficult depending on temperature and acid concentration. At 90°C and with the liquid/solid ratio of 20 L/kg, more than 95% of zinc is recovered in 30 minutes with 0.5M H2SO4. To attain similar recovery for manganese, higher levels of acid concentration and time are needed (e.g 0.7 M and 2 hours). After leaching a purification step is necessary to remove iron co-dissolved through Fe(III) precipitation. Separation of zinc from manganese by solvent extraction with 1M DEHPA follows in the process route. The countercurrent multistage separation diagram developed allows the production of a zinc electrolyte with 120 g/L Zn and 0.005 g/L Mn, and a raffinate with 16 g/L Mn and 0.013 g/L Zn.IntroductionThe recycling of spent Zn-MnO2 batteries is carried out by dedicated recyclers using several process alternatives [1]. Most of the running processes use pyrometallurgical technologies [2] based on zinc distillation. Alternative treatments by hydrometallurgy have been reported [3-5] but its application is scarce.In order to contribute to the development of alternative solutions, a process for recycling batteries based on Zn-MnO2 systems has been studied. The process is based on the hydrometallurgical treatment of spent batteries in sulfuric acid media (Figure 1). The process starts with the physical processing by shredding using cutting grinders, where the batteries are opened and size reduced, allowing the liberation of the interior electrode particles or pastes. The fines can be then separated and the coarse material containing the steel scrap can be treated to remove the remaining aggregate electrode. The final scrap also contains some plastics and other non-metal materials and can be further valorized."

Jan 1, 2008

By Dan Wang, Qian Li, Yong-bin Yang, Tao Jiang

"Thiosulfate is one of the most promising non-cyanide lixiviants for gold leaching. However, the undesirable reaction between thiosulfate and copper (II) gives rise to increased reagent consumption, which results in high cost and huge limit to its development. This paper presents study on the effect of ammonia, copper (II) and Cu(NH3)l+ ions on the oxidative decomposition of thioulfate. It shows that the presence of copper (II) and Cu(NH3)l+ can significantly increase the thiosulfate oxidation, while ammonia is relatively unaffected. The oxidation of thiosulfate by copper(II) in the absence of ammonia is fast at first and then decreases as time increased within a certain time, which can postulate that an intermediate product is responsible for the decreased consumption. The effect of ammonia is depended on the interaction with copper (II), which was found to significantly affect the consumption of thiosulfate.IntroductionFor over one century cyanidation is widely used in industrial production of gold, due to its simplity of process and low cost of production. However, cyanide is a highly toxic chemical reagent used dangerously and brings serious environmental pollution. What's more, cyanidation has slow speed of leaching gold and poorly leaching effective for refractory ores. With the exhausting of free-milling gold ores and promoted environmental protection requests, the disadvantage of cyanidation becomes a growing problem. In recent years, more and more research activities have been focused on alternative processes using non-cyanide lixiviants. Among the non-cyanide lixiviants, thiosulfate is considered as the most promising one[l-5].Compared to cyanide, thiosulfate is an inexpensive, nontoxic and less-pollution reagent, which can form complexes with many metal ions. Thiosulfate leaching of gold has an acceptable leaching rate and is insensitivity to impurities. Moreover it presents advantage on the treatment of refractory gold ores such as carbonaceous gold ores, copper gold ores, complex arsenic and sulfur gold ores, and so on[6]."

Jan 1, 2013

By Beatriz Amarai Campos, Jorge Alberto Soares Tenorio1, Denise Crocce Romano Espinosa, Adriana Johanny Murcia Santanilla

"The aim of the present work is to investigate the recovery of nickel from obsolete cell phones printed circuit boards. The printed circuit boards were firstly submitted to a grinding process and then leached in sulfuric acid. Nickel was extracted from aqueous solution using Cyanex 272. Aqueous/organic ratio was 1/1. The effect of both pH and modifier addition on selectivity of extraction was investigated.IntroductionCurrently, electric and electronic equipments (EEE) have become a necessity to the modern life. Associated with this necessity comes the continuous and increasing replacement of those equipments by new ones. The accelerated technology advances are responsible for the generation of electric and electronic waste. This waste can be dangerous not only to human health but also to the environment. Waste of electric and electronic equipments (WEEE) has a variety of components and metals in its composition becoming a potential pollutant to the environment when not properly discarded. Its wrong disposal causes a loss of materials that could be recovered and reused. Therefore WEEE treatment is an important matter because it can assist the reduction of waste generated and the recovery of valuable metals.Printed circuit board (PCBs) is an essential component of EEE and is typically very complex from a chemical point of view. Several metals may be present in its composition, such as cooper, nickel, iron, zinc, lead, tin and silver1''. This characteristic hinders the development of a simple treatment, making it necessary the application of chemical and mechanical processing for their recycling'4'. The UN estimates that approximately 20 to 50 million of tonnes of WEEE are generated worldwide each year."

Jan 1, 2011

By Amanda C. Lima, Luiz Augusto H. Terrones, Sergio N. Monteiro

"Fabric from weaved yarns made of jute fibers have been considered as reinforcement for polymeric composites. In particular, these fabrics obtained from discarded sackcloth are presently being investigated as environmentally friendly composites with recycled polyethylene matrix. The objective of the present work was to compare the practical properties and economical aspects of these composites with those of conventional materials such as wooden board and gypsum panels for building application. The comparison showed that, depending on the amount of post-used jute fabric, a cost/benefit analysis favors these composites over the conventional materials.IntroductionThe increasing amount of wastes generated by human activities is becoming a worldwide problem of pollution with growing consequences to the environment. The question on how to dispose these wastes is, therefore, a major global issue. Among the possibilities of it gating the problem, the use of materials with characteristics of being renewable, biodegradable and recyclable is considered an environmentally correct solution. Examples of this type of materials are left over lignocellulosic fiber from coconut husks and sugarcane bagasse [1] that, after the primary extraction of edible pulp and juices, can be recover for industrial application. Nowadays, the main use of these fibers is to reinforce polymeric composites applied as components for building construction and automobile parts [2,3]. In addition to these applications, composites reinforced with residual lignocellulosic fibers may replace conventional furniture and panels made of wood and thus help to reduce deforestation [4].Environmental protection is not the only motivation for recycling natural fiber wastes. In developing regions activities associate with collecting and processing residual fibers provide job opportunities for low-income people. Moreover, if the lignocellulosic fiber is collected as a recyclable waste, it hes the economic advantage of a comparatively cost, which constitutes in a relevant difference as a choice for commercial utilization."

Jan 1, 2008

By H. Tan

?Preg-robbing? is the active adsorption of gold from cyanide solution by the ore components. The role of carbonaceous coatings on chalcopyrite surfaces in the preg-robbing of chalcopyrite has been investigated by using pure chalcopyrite and a copper concentrate. Activated carbon and graphite were chosen as representative carbonaceous contaminants. It was found that the carbonaceous coatings enhanced the preg-robbing of chalcopyrite. Activated carbon coating increased gold adsorption onto chalcopyrite to a lager extent, in comparison with graphite coating. In the preg-robbing of the copper concentrate, gold adsorption was increased to larger extent at finer particle sizes and at higher contents of activated carbon or graphite. The preg-robbing of chalcopyrite was reduced or eliminated, depending on the concentrations of free cyanide. However, the gold adsorption on the carbon and graphite coated chalcopyrite could not be avoided even at higher cyanide concentrations, and this adsorption was solely attributed to the carbonaceous coatings. Zeta potential studies indicated that the carbonaceous coatings reduced the negativity of the chalcopyrite surface charge. As shown by SEM analysis, gold not only accumulated at the edges and defect sites, but was also spotted on the smooth surfaces of chalcopyrite with carbon or graphite present. XPS results revealed that gold was strongly reduced on chalcopyrite surfaces, with the sulfide ions of the chalcopyrite being oxidized to elemental sulfur. Diagnostic elution indicated three mechanisms contributing to gold take-up by chalcopyrite, i.e. gold reduction, physical adsorption and chemical adsorption.

Jan 1, 2003

By Riyad N. Ahmad-Bita, Shadia J. Ikhmayies

"SnO2:F/CdS:In structures were prepared by the spray pyrolysis technique on glass substrates at a substrate temperature Ts = 450°C. NH4F and HF were both tried as the sources of fluorine in the precursor solution of SnO2:F. A comparison between the properties of structures obtained by using the two doping compounds was performed. X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmittance measurements were used to characterize the films. The structures prepared by using HF as a fluorine source were found to have more ordered crystal growth, larger grain size and sharper absorption edge. From the inspection of the first derivative of the absorbance it is expected that more interdiffusion on the SnO2:F/CdS:In interface takes place in the structures made by using HF. These results confirm that these films are better as forecontacts for CdS/CdTe solar cells.IntroductionThin film CdS/CdTe solar cells built in the superstrate geometry rely on transparent conducting oxides (TCOs) to make the front contact The investigation of combined CdS-TCO films has recently been developed owing to the great interest of better understanding the effect of these bilayers on the absorbers [1]. Usually SnO2 is utilized as a front contact for these solar cells. Optimizing the properties of the SnO2/CdS structures is an important step on the way to get high performance CdS/CdTe solar cells.There are different methods to prepare SnOz thin films, such as reactive sputtering [2], evaporation [3], chemical vapour deposition [3, 4], dip coating [5] and spray pyrolysis [6-9]. At the same time CdS thin films can be prepared by different techniques such as chemical bath deposition [10], thermal evaporation [11], screen printing [12] and spray pyrolysis [7, 13]. However, the spray pyrolysis technique is a very low cost and simple technique that enables intentional doping and getting large area and uniform thin films [14]. For these reasons it is choused to prepare SnOz and CdS thin films in this work. To improve the properties of these compound semiconductors, SnOz was doped with fluorine and CdS was doped with indium where such doping is well known for these compounds."

Jan 1, 2012

By Fu-Shen Zhang, Mengjun Chen, Jianxin Zhu

"A novel approach for foam glass preparation, namely vacuum-aided powder sintering technique, was preliminarily investigated in the present communication. The key point of which was to prepare foam glass at a negative pressure. Compared to normal powder sintering process, the new approach could benefit the foaming process by shorting the holding time, reducing the amount of foaming agent and especially decreasing relative density of the product. Optimum conditions were 750 °C, 1000 Pa, 5 min and 1 wt.% foaming agent, respectively.IntroductionFoam glass represents a highly valuable solution for thermal and acoustic insulation, since it possesses a generally higher mechanical, chemical and thermal stability than other foams'1'. The first industrial processing for foam glass production, the direct introduction of gases (""blowing"") into the special molten glass, can be dated back to the end of 1930s'2'. At present, almost all foam glasses is prepared by powder sintering technique instead of blowing,3 since it reduces the temperature by several hundred degrees. Moreover, as fine glass powders or similar powders can be used to substitute corresponding glasses by this technique, considerable attention has been focused on the production of foam glass by considering fully recycled glasses, coal fly ash, or other solid wastes as raw materials,4 especially CRT glasses'3' 5', on the point of environmental protection.In a previous report'6', when discussing the lead removal and recovery from CRT funnel glass by a pyrovacuum process, we found that foam glass could be prepared at a negative pressure. Therefore, in this communication, the similarities and differences between the powder sintering process for foam glass at normal and negative pressure was preliminarily discussed."

Jan 1, 2011

By Jie Li, Liangxing Jiang, Yexiang Liu, Junfeng Gui, Bo Hong, Xiaocong Zhong, Yanqing Lai, Xiaoying Yu

"Pb-based alloys with Pr and Ag were prepared in vacuum electromagnetic induction furnace. The tensile strength, corrosion rate and anodic potential in sulfate solution were measured, and the experimental data were analyzed according to the metallographic phases of alloys, the micromorphology and composition of their oxide films. The results show that, with the addition of Pr, the ultimate tensile strength and corrosion rate of pure lead were increased, and the anodic potential decreased. The extra addition of Ag can improve the properties of alloy further. Comparing with Pb-Ag0.8 alloy which is widely used in zinc electrowinning industry, the ultimate tensile strength of Pb-Ag0.6-Pr2.0 alloy was increased by 31.75%, the anodic potential under 50mA/cm2 was decreased by 30m V.IntroductionIn zinc electrowinning industry, the Pb-Ag (0.5-1.0 wt.%, 0.8wt.% normally) anode is widely used as an insoluble anode['l. It can meet the basic requirements, but still has several problems such as high oxygen evolution over-potential (about 860mV), unsatisfactory corrosion resistance, lead contamination of the cathode product and high consumption of Ag etc.In order to reduce the energy consumption, enhance the corrosion resistance, improve the product quality and reduce the consumption of Ag (or even dispense with it), much research has been done, mainly focusing on Pb-based alloy anodes and Ti-based coated anodes. Detailed investigations have already been carried out on binary alloys (Pb-Ca and Pb-Co), ternary alloys (Pb-Ag-Ca, Pb-Ag-Ti, Pb-Ag-Sn, Pb-Sr-Sn, and Pb-Ca-Sn) and quaternary alloys (Pb-Ca-Sr-Ag, Pb-Ca-Ce-Ag, and Pb-Ag-Sn-Co)[Z-4l, Although these anodes can effectively reduce the consumption of Ag, only the Pb-Co and Pb-Ag-Sn-Co anodes perform well with regard to reducing the anodic potential. However, their complicated manufacturing conditions restrict further commercial use.Besides its application in nonferrous metal electro-winning industry, Pb-based alloy is also used as grid alloy for lead-acid battery, serving as active materials supporter and current collector. In order to enhance the corrosion resistance and deep-cycling performance, reduce the impedance of the corrosion film, the addition of appropriate rare earth elements into anodic grid alloys has become a research focus. Studies proved that RE can enhance the mechanical strength of grids, inhibit the formation of anodic Pb(II) film on the surface of grids and then reduce the impedance of the film[ 10-12l."

Jan 1, 2013

By Suleyman Tekeli, Serdar Salman, Bulent Aktas

"The effect of La2O3 content up to 15 wt% on phase stability, sintering and microstructure of cubic zirconia (8YSZ) was investigated. XRD results showed that the specimens containing up to 15 wt% La2O3 were composed of only cubic structure. Also, the specimens doped up to 5 wt% La2O3 revealed no La2O3 peaks, indicating that La2O3 was completely solubilized in the cubic structure. However, when> 5 wt% La2O3 was added, the peak of La2Zr2O7 compound emerged, showing that the overdoped La2O3 was not solubilized in the 8YSZ matrix. The lattice parameter of the 8YSZ slightly decreased with the increasing La2O3 content up to 1 wt% but further increase in the La203 amount resulted in an increased lattice parameter. The comparison of grain size of the 8YSZ specimens with various La2O3 content showed that grain size slightly increased with the increasing La2O3 content up to 1 wt% but further increase in the La2O3 amount resulted in a decreased grain size.IntroductionAt atmospheric pressures, three polymorphic forms of Zr02 are stable at different temperatures i.e. monoclinic, tetragonal and cubic. A high-pressure orthorhombic form of Zr02 has also been reported[l]. The successful production of pure Zr02 bodies is not possible all the time due to the large volume expansion associated with the martensitic tetragonal-monoclinic transformation. This fact restricts the applications of zirconia, in spite of its excellent mechanical and thermal properties. However, the stabilization of the high temperature polymorphs at room temperature as stable phases is made possible by addition of suitable dopants. Fully stabilized cubic Zr02 and partially stabilized tetragonal Zr02 show interesting properties and are widely used as ionic conductors, coatings and gas sensors in solid oxide fuel cells and structural applications[2]. Most frequently used dopants include Y203, CaO, MgO and Ce02, although other oxides, such as those of rare earth elements, can also act as stabilizers of the high temperature structures. The incorporation of aliovalent cations to the lattice, forming substitutional solid solutions, allows to control the concentration of anionic vacancies in the structure. This aspect is particularly important in designing ionic conductors[3], and is also determinant in the stabilization process[ 4]. The process of stabilization with larger ionic radii dopants is rationalized by the crystal chemistry model[ 5], that describes the dopant cations as typical stabilizer when they have larger ionic size, lower charged state and higher ionicity than Zr4+ The ionic radius of Zr4+ is 0.84 Å and that for La3+ is 1.016 Å [6]."

Jan 1, 2012

By Masatsugu Morimitsu

"The novel smart anode, MSA ™, for electrowinning of non-ferrous metals such as copper, zinc, nickel, and cobalt has been developed by thermal decomposition. The smart anode consists of a titanium substrate coated with a catalytic oxide layer which comprises amorphous or less crystalline oxide coatings. The catalytic layer contains an iridium oxide-based mixture or a ruthenium oxide-based mixture. The smart anode provides a remarkable reduction in cell voltage compared to other anodes, e.g., commercially available coated titanium electrodes and lead alloy electrodes. The test data has demonstrated that a maximum voltage reduction by ca. 30% is possible compared to lead alloy anodes. The smart anode also gives some additional merits in suppressing unwanted deposits on the anode; i.e., deposition of MnOOH, Pb02, or CoOOH. The electrowinning with the smart anode is possible to be an environmentally friendly process with less energy consumption and less anode deposits.IntroductionA coated titanium electrode iridium oxide-based or ruthenium oxide-based catalytic layers is well known as an insoluble anode for oxygen or chlorine evolution in industrial electrolysis such as chloro-alkali electrolysis, electrogalvanizing or electrotinning of a steel, a thin film production by electrodeposition such as copper foil production (CFP), water electrolysis, and electrowinning of nonferrous metals. The anode is commercially produced by thermal decomposition of a precursor solution painted on a titanium substrate, and the decomposition is usually performed at 450 °C or more. The obtained catalytic oxide coating formed on the substrate contains crystalline oxide as an active component to oxygen or chlorine evolution. The author of this paper had met a problem of such a crystalline oxide coating in the application of copper foil production; the anode was unable to use for a long period because of a large amount of lead oxide (Pb02) deposited on the anode, and the cell voltage was seen to continuously increase and drastically rise by the accumulated Pb02. In this case, the voltage reduction by replacing a lead alloy anode with the dimensionally stable anode was initially observed, but was gradually lost and disappeared. Therefore, the author of this paper aimed and investigated to suppress the unwanted side reaction on the anode, and finally invented a new class of coating based on an amorphous iridium oxide mixture in 2003 [!]. The invented coating was obtained at a low temperature thermal decomposition, e.g., 360 °C, and the coating consisted of amorphous iridium oxide and amorphous tantalum oxide. This invention achieved that oxygen evolution potential shifted more negative so that the cell voltage was reduced, and no Pb02 was deposited in the electrolyte of CFP [2,3]."

Jan 1, 2012

By Larry M. Southwick

Pneumatic converting (Bessemerizing) of iron revolutionized the steel industry. Bessemerizing of copper (conversion of copper sulfide matte to copper metal) was proposed at almost the same time, but it was slow in being accepted. The differences between iron and copper converting were great and technical problems were substantial. It took 25 years for the process to become viable and another 25 years before a truly economical solution was found. A major economical and productivity problem was the short life for converter refractory linings. The first converters had acid (silica) linings, which were quickly consumed since silica was a flux for the process. Converters had to be relined at least once per day, a laboriously expensive manual process with only the most rudimentary mechanical aids available to assist. The industry was revolutionized almost overnight when finally a viable basic (magnesite) lining was developed. This lasted 100's of days versus less than one, leading to converters that were easier to operate and which handled larger charges. This change occurred after W.H. Peirce and E.A.C. Smith, with support from the Guggenheim interests, successfully operated a basic lined converter in a copper refinery in Baltimore. While Peirce and Smith are generally given credit for the development and explosive acceptance of this idea, a Pittsburgh industrialist, Ralph M. Baggaley, working in an independent smelter in Butte, Montana, successfully built and operated a basic lined converter four years before they did. In fact, the early support for Peirce and Smith likely occurred because Guggenheim's staff were encouraged after thoroughly examining Baggaley on his earlier successes. The questions of technology primacy between Baggaley and Peirce/Smith are ironically similar to those between Wm. Kelly and Bessemer in converting iron to steel. This paper will review what Baggaley (and other early researchers) accomplished, examine why he (or they) did not receive credit equal to Peirce and Smith and explore what his (their) place should be in the development of successful basic linings. More suspects than a Victorian Whodunit.

Jan 1, 1999

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