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By J. Huisman

With the introduction of ever-stricter environmental operating guidelines, capital expenditure restrictions and operational budget cutbacks, the biological method of SO2 removal becomes more and more attractive. Biological treatment of dilute flue gases is a more cost effective technology in comparison to conventional sodium hydroxide scrubbing. Although the investment costs for sodium hydroxide scrubbing is lower, the operational costs are significantly higher. In addition, the end product of the biological installation is sulfur instead of sodium sulfate; and no further wastewater treatment of the bleed from the biological installation is required since heavy metals are removed simultaneously. Another option for the treatment of SO2 containing gas at a sulfuric acid plant is the production of extra sulfuric acid of the discharged SO2 by applying an additional converter. Comparing biological treatment with this option shows much lower investment costs for the biological installation. Sulfur is produced which can be converted to sulfuric acid, so the bio-route will be more cost-effective than an additional converter. In principle, the biotechnological gas cleaning system is an integration of an absorber with a wastewater treatment facility. In the absorber, the SO2 containing gas is brought into contact with the washing water. The effluent absorber liquid contains a mixture of sulfite and sulfate that is converted into elemental sulfur. This conversion takes place in an integrated system; first, the sulfite/sulfate mixture is converted anaerobically into sulfide; secondly, the sulfide is converted aerobically into elemental sulfur. Subsequently the sulfur is separated and the water is returned to the absorber. Due to the buffer capacity of the washing water, removal efficiencies over 98% are possible. In addition to SO2 removal, it is possible to convert for example other bleeds streams such as scrubber acid or weak acid to sulfur in the same SO2 installation. Recent evaluations concluded that biological desulphurization of flue gases is not only economically attractive in comparison to convention sodium hydroxide scrubbing but also in comparison to gypsum producing systems and even seawater scrubbers. This paper describes the technological and economical viability of biological flue gas desulphurization.

Jan 1, 2005

By Zhang Chuanfu, Tan Pengfu

"A thermodynamic model is developed to simulate nickel flash smelting process. In the nickel flash furnace, oxidation of concentrate occurs at one end, and reduction of slag occurs at the other. The model makes use two zones, namely the reaction shaft/settler zone and the appendage zone and accounts for 6 phases (matte, slag, silica, magnetite, Cu-Ni alloy and gaseous phase), 13 elements (Ni, Co, Cu, Fe, S, 0, N, C, H, Si, Al, Mg and Ca) and 33 chemical components in nickel flash smelting system. The compositions of matte, slag and gaseous phases in equilibrium are calculated by using the data of free energies of formation and activity coefficients of components. Two nickel sulfide species are used to allow for the modeling of sulfur-deficient mattes. The model predictions are compared with the known industrail data from Kalgoorlie Nickel Smelter, and excellent agreement is obtained. The model can be a very useful tool for monitoring and optimizing the actual industrial operations of nickel smelting process. The distribution behaviors of Ni, Co, Cu, Fe, S and 0 in the nickel smelting furnace depend on the process parameters such as smelting temperature, volumes of air, the content of the elements~ charge and oil.1. IntroductionThe nickel flash smelting furnace essentially consists of a reaction shaft where nickel sulfide concentrate is partially oxidized with air, a settle zone where matte and slag are allowed to separate, and a slag cleaning end where coke is added to provide for the reduction of the oxidized nickel from slag, and electrodes are used to provide heat.The theoretical model to consider a mass balance for copper flash furnace is developed by S. Goto and R. Shimpo[1][2J. However, this can not be true for nickel flash furnace as a whole since oxidation of concentrate occurs at one end (in the reaction shaft/settler), and reduction of slag occurs at the other (in the appendage). Despite these limitations, an acceptable pseudo-thermodynamic description of the furnace can be achieved using essentially two zones, namely the reaction shaft/settler zone and the appendage zone. Compositions of gas, slag and matte in two zones are calculated."

Jan 1, 1998

By Kimiaki Utsunomiya, Yasumasa Hattori, Yoshiaki Mori, Toyokazu Okubo

"The effect of various operating conditions on splashing behavior in a Peirce-Smith converter has been investigated with a 1/5.7 scale cold model. Dynamic similarity between the model and a commercial converter was attained by setting the modified Froude number in the model experiments in· the range for normal converter operation. It is known that for a given modified Froude number the dimensionless penetration length of gas into the liquid phase increases as the liquid density decreases. Moreover, penetration· length has a large effect on splashing behavior. Therefore, a heavy liquid, a mixture of water and lead concentrate was used as the liquid phase. It was concluded that the amount of splash dramatically decreases with a reduction in the buoyancy energy per, unit liquid mass and an increase in the horizontal distance between the tuyere tip and the edge of the mouth.IntroductionSubmerged gas injection is widely used in practice in ferrous and nonferrous pyrometallurgical operations to achieve large gas-liquid contact areas and good agitation of liquid for rapid chemical reaction. The common application in ·nonferrous industry is the Peirce-Smith converter with multi-tuyere for copper and nickel matte converting. This process has been used for over 100 years because of its effectiveness in mixing of the molten bath, as well as its merits of the engineering simplicity. However, the mechanisms which · determine the blowing performance is poorly understood, and the design and operating conditions of the Peirce-Smith converter varies widely from plant to plant, such as by diameter, length, mouth angle, tuyere position and level of molten matte. Smelters have continuously made an effort to increase converter productivity, implying maximum tuyere blowing rate. Above a certain critical blowing rate, splash of molten matte from the converter mouth becomes unacceptable because of dangerous ejection and accretion buildup around the converter mouth, which results in interference with effective hood sealing. In fact, a 1993 converter survey[!] reported that splash was a major limiting factor for blowing rate and 54% of responding plants from around the world regard it as a limiting condition[2]. In order to increase tuyere blowing rate a study of the effect of various operating conditions on splashing behavior is expected."

Jan 1, 2000

By Alex Luyima, Jaan Kers, Lifeng Zhang

"The pyrolysis of PWBs was investigated by a TG-DTA-MS furnace at 300–1173 K. The kinetics and the control of emitted gas during the pyrolysis of PWBs with and without chemical additives were studied. Moreover, the possibility of controlling the amount of toxic exhaust gases like HBr, C6H6, Br2, Cl2, HCl gas and recovering beneficial gaseous fuels like CH4 and H2 from pyrolysis process is discussed. The MS data for each PWB sample were examined as a function of temperature and particular m/z values could be associated with the mass loss steps in the TG data. The degradation of the organic material was characterized by m/z = 2, 16, 18, 28, 36, 44, 71, 78, 81, and 160. Fe2O3 was the best inhibitor of toxic HBr and C6H6 when compared to Al2O3, CaO Y-zeolite and ZSM-5. Moreover, it had no significant effect on the valuable H2 and CH4 gas evolution. This selective inhibition of toxic gases while maintaining the valuable ones make Fe2O3 the best candidate among the investigated additives in controlling gas emissions from PWB pyrolysis process.IntroductionThe electronic and electric industry is one of the world’s largest and fastest growing manufacturing sectors. As a consequence of this growth, electrical and electronic waste (e-waste), such as computers, washing machines, printers, mobile phones, television sets, stereos, radios, etc., is generated in large quantities around the world. Printed wiring boards (PWBs) are a common component of many electronic and electric systems.[1]. The rapid development and expansion of the electronics industry over the past several decades have led to a dramatic increase in the production of PWBs and a corresponding increase in the amount of waste generated from both production and disposal. The environmental impacts of the treatment and recycling of PWBs waste have become a major concern [1-2]. PWBs are particularly problematic to recycle because of the heterogeneous mix of organic material, metals, and glass fiber [1]."

Jan 1, 2012

By Mario H. Castro-Cedeno

"A design for a handheld MEMS chemical detector is proposed. The detector will be used to detect trace amounts of chemicals in air. It can detect drugs, toxic chemicals and/or explosives. The proposed detector will use ion mobility spectrometry (IMS), a technique that is well known for accuracy and has been used in the past in suitcase sized chemical detectors. The separation and detection of the chemicals occurs in the drift channel and the process was modeled using the finite element method and CoventorWare modeling software. A manufacturing process sequence for the drift channel is proposed and was demonstrated.IntroductionThe goal of this effort is to design, mode~ and prototype a MEMS chip that will be the key component in an ion mobility spectrometer (IMS). This technique uses and asymmetric potential to separate the various ion species in a stream of incoming air [1-4]. One advantage of IMS is its ability to separate chemical species from air at atmospheric pressure and temperature. This is a requirement for a simple to use handheld drug or chemical detector. IMS can be used to detect drugs, toxic chemicals and explosives and it is well known for accuracy in detecting very small amounts of chemicals. This chemical detection technique has been used in the past, but not in handheld detectors.One variant of IMS is the high-field asymmetric waveform ion mobility spectrometry or FAIMS [3]. The FAIMS process, shown in Figure l, works as follows: a gas sample is admitted into the instrument where gas molecules are ionized, typically by a weak radioactive isotope source, ultraviolet light source; and more recently through field emission. The ions move along the length of a channel while they are separated in the transverse direction by an asymmetric electrical potential. The potential, in the form of an asymmetric waveform, causes relative motion between the various chemical species. The species that hit the charged top and bottom plates are neutralized and only those ions that move along the center are detectable as charged chemical ions at the end of the channel."

Jan 1, 2004

By Qingchun Yu, Baoqiang Xu, Yongnian Dai, Bin Yang, Fulong Zhu

"In this paper, the mechanism of the carbothermic reduction-chlorination process to extract aluminum from alumina in vacuum was investigated. The carbon monoxide (CO) content of the gas, phases of the reduction slag, surface morphology of the reduction slag and the product aluminum were measured by means of gas chromatography (GC), XRD, and SEM. The experimental results indicated that the content of CO in the gas decreased, but Al4C3 increased with time at 1773K during the carbothermic reduction process of alumina. AlCl(g) and graphite (C) were produced by the reaction between Al4C3 and AlCh(g) at 1773K, and then aluminum beads generated after the decomposition of AlCl(g). It implied the mechanism of alumina carbothermic reduction-chlorination process in vacuum involves three steps as follows: the carbothermic reduction of A}z03 to produce Al4C3, the chlorination of Al4C3 by AlCh(g) to produce AlCl(g), and the decomposition of AlCl(g) to produce Al(l).IntroductionAluminum is the basic raw material for many industries [1], and it is used extensively because of various excellent properties such as light weight, good malleability, high strength, excellent thermal conduction, high corrosion resistance and so on [2]. Industrial production of aluminum currently includes refining alumina and electrolytic aluminum processes. However, its development has been effected by some factors such as high energy consumption and heavy environmental burdens [3]. In the past several decades, there had been numerous attempts to produce aluminum by new methods. Extracting aluminum from alumina or bauxite directly by carbothermic reduction-chlorination process had been studied [ 4-6]. Although the alumina carbothermic reduction process [7~9] had been studied, the mechanism of the carbothermic reduction-chlorination process had not been systematically elucidated.In order to investigate the mechanism of the carbothermic reduction-chlorination process in vacuum, GC, XRD and SEM techniques will be used to determine the CO content and to characterize the surface morphology and composition of the slags at various temperatures."

Jan 1, 2011

By Wayne Bell, Xiaodi Huang, Matthew Andriese, Jiann-Yang Hwang, Zhiwei Peng

"The equations for determining microwave field attenuation length and half-power depth in magnetic materials were derived from Maxwell’s equations. The microwave field attenuation length and the half-power depth for a magnetite concentrate were calculated and the temperature dependence of them was determined. It is demonstrated the microwave field attenuation length and the half-power depth highly depend on temperature and decrease with increasing temperature up to 900 °C. The variations of field attenuation length and the half-power depth with temperature indicate the microwave power attenuates much faster than the field strength in materials. The evaluations of field attenuation length and microwave half-power depth can be used to characterize the microwave dissipation behaviors in the sample and optimize the dimensions of the material in microwave heating.IntroductionMicrowave has been applied in materials processing for its distinguished advantages including rapid heat transfer, volumetric and selective heating [1,2]. However, most research work involving microwave heating are confined to non-magnetic materials (e.g. ceramics), with limited attention paid to the heating of mixed property materials (e.g. magnetite and other ferrites) under microwave irradiation [3-5]. Since many magnetic materials exhibit good and even better microwave absorption capability than non-magnetic counterparts, it is quite necessary and deserved to take advantage of this property and then improve the heating efficiency. To achieve this aim, further understanding on the microwave heating mechanism, especially the microwave propagation/dissipation behaviors in magnetic materials is required.The dissipation behavior of microwave in materials has been identified as one of the key factors that affect the efficiency of heating under microwave irradiation and this behavior can be characterized by several parameters. Apart from traditional penetration depth (TEM power penetration depth, Dp = 1/(2*a), where a is the TEM field attenuation factor), two other parameters, field attenuation length (Df) and half-power depth (Dh), are also applied to indicate the microwave dissipation in materials [6].The accurate determination of such parameters can help in optimizing the dimensions of the load in a microwave furnace, producing more uniform heating under microwave irradiation and avoiding thermal runaway."

Jan 1, 2011

By A. Hasko

Phytoremediation is a new low cost alternative technique for remediation of contaminated soils from heavy metals that are emitted by ferrous and nonferrous mining and extracting processes. It is based on the possibility to use several plants that accumulate high level of metals in order to remove metallic pollutants from soils and render them harmless. Phytoextraction is an adjacent new technique that uses these hyper-accumulator plants in order to extract the metals from them using even the conventional smelting or refming processes. In our previous work, an extensive investigation of about 150 plants have been carried and several species were identified that could be used for nickel phytoremediation and phytoextraction because of their high accumulation of nickel. It has been found that five taxa from Alyssum genus specie had the highest ability to accumulate nickel with concentrations more than 10000 ug/g (dry weight) or 1%. The taxa showing the highest accumulation of this metal is Alyssum murale var. chlorocarpum with 28 600 ug/g or 2.86%, a good candidate for Phytoextraction. In this work, in order to optimize the phytoremediation and phytoextraction processes further Absorption Spectrometry measurements and biological studies were carried out to determine the parts of the plants that accumulate the highest amount of nickel and the best biological cycle during which they accumulate the highest amount. The results show that the greatest accumulation of nickel occurred in the leaf material (2.86%) and the least in the roots (0.43%). The investigation of the biological cycle of the genus Alyssum showed that: (1) the seeds germinated between 50 C to 30 0 C and more in 25 0 C; (2) 62.9 % of seeds germinated at A.m. var. chlorocarpum; (3) the emergence is almost continue from March to April; (4) the anthesis occurs from May to July; (5) the ripening of the fruit takes place 30 days after flowering; (6) the dissemination of fruits occurs from September to October. Due to these special characteristics it is reaffirmed that Alyssum murale var. chlorocarpum, as a nickel hyperaccumulator, is the most promising plant to be used for feasible phytoremedation and phytoextraction purposes. Keywords: Key words: Phytoextraction, PhytoRemediation, Nickel accumulators, Alyssum sp., Biological cycle

Jan 1, 2003

By S. C. Sharma, M. Krishna, N. Sanmukha

"The oxidation behavior of an aluminium composite with 0, 2, 4, and 6% by weight of hematite at 200 to 500 °C has been investigated. Within the experimental temperature ranges a parabolic weight gain was observed. The, weight gain as a function of oxidation time becomes linear after an initial period on oxidation formation, an oxide scale was found whose morphology depends on temperature, cooling rate and sub-scale formation at the interface between the matrix and reinforcement. The presence of hematite particulate reinforcement has very little effect on the oxidation behavior. The interface oxidization rate was found to be higher than that of other regions. The, oxidation products were either metallic oxides or ceramic oxides. The exposure time of specimens to oxidation was 1000 minutes at various temperatures. In the present work key principles of alloy oxidation were discussed. Also the paper emphasizes various reactions taking ' place and the activation energies involved in the oxidation reactions.IntroductionMetal matrix composites (MMCs) reinforced with ceramic particulate, whiskers, or fibers have received increasing attention due to their potentially high fracture toughness and strength 1-5. Particle reinforced Aluminium MMCs find potential application in several thermal environment, especially in the automobile engine parts, space applications, such as drive shafts, cylinders, pistons, and brake rotors6.With the exception of gold, no metal or alloy is stable at room temperature, they tend to form their respective oxides. Most of the metals in the solid or liquid state are morphologically unstable when exposed to air at higher temperatures. An investigation relating to the temperature profiles of the piston area in a diesel engine has shown that the temperature can reach as high as 500¬800 K in certain regions of the piston. As the piston and cylinder areas are exposed to high temperature environment, the MMCs should have sufficient stability on both mechanical and chemical strength (oxidation). Oxidation occurs at grain boundaries in alloys and at the interface of the particulate and matrix in MMCs, which usually enhances intergranular fracture, resulting in premature failure and severe brittleness 8-10. Therefore for high-temperature applications, it is essential to have a thorough understanding of the oxidation behavior of aluminium MMCs."

Jan 1, 2000

By Guo-hua Bai, Hong-jing Yuan, Qian Li, Yong-bin Yang, Tao Jiang, Yan Zhang

"The effect of different additives on the bio-oxidation of arsenic-bearing gold ores has been carried out to solve the problems such as long period of leaching, low oxidation rate. The oxidants strengthen the cathodic reaction and thus improve the leaching rate by the increase of electron transfer. Meanwhile, silver catalysis is also effective for the decomposition of arsenicbearing gold ores due to the strengthening of anode reaction. Co-intensification by oxidants and Ag (I) is more efficient to the bio-leaching and the conversion of As (III) because the anode and cathodic reaction of biological oxidation of sulphide ores were both strengthened. The leaching rate reached to 63.94% after bio-leaching 13days by co-intensification of Ag (I) and Fe(III).IntroductionWith the worsening global ecological problems and the gradual exhaustion of available gold resources, metallurgical technology of refractory gold ore has received more and more attention and become possible due to its good advantage of the economic effects and negative effects to the environment. Refractory gold ore, the direct cyanide leaching rate of that is defined as less than 70%, has become an important raw material in gold extraction industry, in which sulfide bearing gold ore represents a large proportion, pyrite and arsenopyrite (FeAsS) is a common gold-bearing mineral. Since the gold is often encapsulated in the crystal lattice of these minerals, destruction or alteration of the ore to liberate the submicron and/or structurally bond gold is necessary[l]. Even if the ultrafine grinding approach also is generally not sufficient for these refractory ores and additional techniques like roasting, pressure oxidation and bacterial oxidation are used to liberate the gold [2]. In the three pretreatment processes, bacterial oxidation is characterized by its new ideas, low cost, no pollution, simple equipment and operation, high leaching index and become the most promising process which has received much attention over time [3-5]. But its further application is limited by some of its own shortcomings, such as long pretreatment time and the toxic effects of arsenic to bacteria on bio-leaching limit."

Jan 1, 2013

By Gowda H. S. Desai, A. Herbert Mervin, P. G. Mukunda

"The mechanical properties of cast iron depend on the graphite morphology and characteristics of metallic matrix. In spheroidal graphite iron these properties are affected by the nodule count, nodule percentage, nodularity, nodules per square mm, nodule types and size distribution. In this work an attempt is made to study of the effect of centrifugal and gravity casting process on the morphology and mechanical properties. A comparison of microstructure and mechanical properties of specimens of the cast are studied. It has been observed that the centrifugal effect produces an increase in rupture strain but hardness is unaffected. In microstructure it has been observed that the centrifugal effect produces an increase in the number of bigger nodules and decrease in the number of smaller nodules and an increase of nodules per square mm. It has no effect on nodularity percentage. The centrifugal casting process produces better mechanical properties.IntroductionCast iron, the first man-made composite, is at least 2500 years old. It remains the most important casting material, with over 70% of the total world tonnage [1,7]. The main reasons for cast irons longevity are its wide range of mechanical and physical properties coupled with its competitive price [l]. Gray cast iron is traditionally used in many industries because it is characterized by a flexibility of use, excellent castability, low cost, wide range of achievable mechanical properties. Gray cast irons are selected according to their tensile strength, high modulus of elasticity, good wear resistance and good machinability are desired and for this a high-strength cast iron is selected [2].Flake Graphite and Spheroidal Graphite irons are predominantly being used to manufacture heavy automobile components throughout the world. The properties of gray iron castings are much dependent on foundry practice. Perhaps the most interesting feature of the family of cast irons is the morphology of the graphite phase, which occurs as a result of changes in chemical composition, melting, melt handling techniques and the process of solidification and subsequent cooling. The significance of these differences through graphite morphology is observed primarily in their effect on the physical and mechanical properties of the iron, but in the foundries these are also known to influence the ability to manufacture sound and dependable castings."

Jan 1, 2013

By Maria Margarida Lima, Maria Lucelinda Cunha, Dora Algarvio

"The main goal of the present work is the quality improvement of the recycled aggregates produced by a construction and demolition waste (C&DW) recycling facility located in Montemor-o-Novo, Portugal. The recycling process was developed on a pilot plant scale with 50 t/h of capacity. Process operations are the hammer mill comminution, magnetic separation and screening.In order to improve the knowledge on the C&DW, a characterization procedure was implemented by hand-sorting, magnetic and density separation on representative samples. On the other hand, to improve the quality of the produced aggregates, the bar screen size fractions were analysed, according to the Portuguese Standard (NP EN 933-1 2000).Wood was identified as the critical contaminant, representing 17% by weight of the total contaminants. Sieving results showed that about 97%, 76%, 56%, 98% and 57% were on the correct size range, which lower results are probably due to the type of screens and/or the material characteristics of the recycled aggregates.IntroductionThe construction and demolition waste problemConstruction and demolition waste (C&DW) is generated by the construction activity, resulting from both, buildings or other structures construction and old structures demolition. As a reference, it can be told that C&DW comprises about 40 to 50% of rubbish (concrete, asphalt, bricks, blocks and dirt), 20 to 30% of wood and related products and 20 to 30% of miscellaneous wastes [1]. In Portugal, C&DW is classified in the LER (Portuguese nick name for the European Waste List), Chapter 17, and includes a diversity of wastes, like concrete, bricks, ceramics, bricks, wood, glass, plaster, copper, zinc, lead, iron, steel, as well as insulation and roofing materials. C&DW stream has several characteristics which make it particularly difficult to deal with and are summarized in the following five items.(1) Lack of information on quantities generated: In Portugal, the C&DW sector has been neglected over the past years, which meant that there are not consistent information concerning the quantities and composition of these wastes yet. Several estimates, based in different assumptions, indicate different results, which may vary from 219 Mt to 10 931 Mt [2]."

Jan 1, 2008

By Zhangm Mingming

Three samples received from the EAF shop were characterized by chemical, X-ray diffraction (XRD), optical microscopy (OM) and scanning electron microscopy (SEM) methods. The objective of this characterization work was to investigate the occurrence of nickel, copper, zinc, sulfur and phosphorus and to identify their origin and associations with iron minerals in the concentrate samples from the mines. The samples were identified as MINERAL, PELLET, and HRD. The latter is the DRI product. All three samples were received as fine powders. The results indicate that, in the mineral sample, magnetite is the major iron oxide mineral with hematite as a second phase based on the OM and XRD studies. Pyrite [FeS2], chalcopyrite [CuFeS2] and bravoite [(Fe,Ni)S2] are the major sulfide minerals. Trace amounts of apatite [Ca5(PO4)3(F,Cl,OH)], wardite [Na4CaAli2(PO4)8(OH)8 6H2O], giniite [Fe;(PO4)4(OH)3 2H2O] and vivianite [Fe3(PO4)2 8H2O] were identified by SEM and XRD. Microscopic studies also indicated that most of the sulfide grains in the mineral sample are present either as liberated fine particles (about 10 microns) or as inclusions within the magnetite and hematite grains. XRD studies revealed magnetite as the major mineral with subordinate amounts of hematite and pyrite confirming the microscopic findings. Copper, nickel, and zinc are mainly present as chalcopyrite, bravoite, and franklinite [(Zn,Mn,Fe)(Fe,Mn)2O4] in trace amounts in the mineral samples, respectively. Impurities carry over to the pellet and HRD samples. Chemical analyses of the three iron-bearing samples indicate that sulfur and phosphorus in the pellet sample exceeded the specification. Since liberated pyrite and chalcopyrite particles were observed in both the mineral and pellet samples, magnetic and flotation processing routes should be effective for sulfide removal but at the cost of iron losses. The high phosphorus content of all three samples indicates that there are phosphates which are difficult to remove by the current concentrating processes (magnetic separation and flotation).

Jan 1, 2012

By K. A. Lewandowski

Agglomeration of ore can be used to immobilize fine particles during heap leaching by agglomerating them into granules. Without agglomeration, the fine ore particles can migrate within the heap, clogging flow channels and producing large areas where access of solution to the ore is very poor. The benefits of agglomeration are well-known in gold heap leaching operations, which can be effectively agglomerated using binders such as Portland cement due to the alkaline leaching solutions used. However, agglomeration has not been very effective in the heap leaching of copper ores, because these ores require an acidic leaching solution. Acid destroys the effectiveness of most binders, causing the agglomerates to disintegrate as soon as the leaching solution is applied. In order to gain the benefits of agglomeration in copper heap leaching, an economical, acid-resistant binder is needed. The two issues that needed to be addressed were: 1) Lack of effective methods for evaluating binder acid resistance before performing expensive, time-consuming, full-scale heap leaching tests, and 2) The vast majority of known binders react poorly to acid conditions, and so a basis was needed for determining which binders are most likely to be acid-resistant. In this paper, the development of two new tests for evaluating binder acid resistance in the laboratory are described. The ?soak test? determines the degree to which agglomerates disintegrate and release fines on contact with acidic solution, measuring the relative quantities of fines released by agglomerates made with different binders under controlled conditions, and serves as a rapid means for comparing large numbers of binders. The ?percolation test? measures several different parameters to determine how a binder is likely to perform in heap leaching: 1) the degree of ?slump? and compaction of agglomerates as they are wetted by acidic solutions; 2) the hydraulic conductivity of the agglomerate bed; 3) the migration of fines through the bed as the solution flows through it; and 4) the quantity of liquid retained in the agglomerates after they are drained. Using these tests, a broad spectrum of binders were examined. Soak testing determined that the most acid-resistant binders were nonionic polymers. Five of these binders were further evaluated using percolation testing.

Jan 1, 2006

By Signe Kjelstrup, Leiv Kolbeinsen, Marit Takla, Odne Burheim

"This paper presents a Seebeck-type solid state thermoelectric power generator unit, designed to investigate the possible recovery of radiant waste heat at a silicon plant in Norway where roughly 703 of the total input energy leaves the process as waste heat. The unit is 0.5 m x 0.5 m and is built of 36 commercially available thermoelectric devices based on bismuth telluride p - and n - type semiconductors. Thermoelectric devices directly convert fractions of a heat flux into an electric current (and vice versa) and may therefore be convenient for recovery of waste heat when the heat source is discontinuously available. The purpose of the thermoelectric unit is to give a proof of principle of direct thermoelectric energy conversion on a large scale. We present the initial test results for the generator. At an average temperature difference between the heat reservoir and the heat sink of 98°C, we measured an open ciruit potential of 23.44 ± 0.06 V and the matched load power output was 39.4 W. At a temperature difference of 220°C, we predict the generator open circuit potential to be 40.8 V, which corresponds to an efficient Seebeck coefficient of 242 µV /K, and matched load power output to be 120 W.IntroductionThe world's power demand increases, driven by population growth and increase in living standards and simultaneously global warming is recognized as one of our most serious environmental problems. According to the International Energy Agency[l], the industrial sector accounted for approximately one third of the total global power consumption in 2005. Increasing the energy efficiency of industrial processes thus represents a benign and substantial route for addressing environmental concerns and energy security.In accordance with the second law of thermodynamics, all real processes are associated with lost work which is energy being dissipated as heat to the surroundings[2]. Improving the energy efficiency of industrial processes is about finding the process path associated with a minimum of lost work. The more evenly the losses are distributed, the smaller are the losses [3, 4]. In addition, exploiting the unavoidable waste heat will contribute to improve the energy efficiency. The waste heat may be utilized for heating purposes and/or it can be upgraded to work for instance via some sort of heat engine."

Jan 1, 2012

By R. C. Chaturvedi, S. B. Padwal

"Padwal and Chaturvedi have developed the model based on M-K theory, considering Hosford's yield criterion and critical thickness strain criterion"" to predict the sheet metal forming limits under simple (constant) strain ratio paths. This analysis has been extended in this paper to predict the sheet metal forming limits under complex strain paths. The effects of exponent ""a"" in Hosford's yield criterion and strain paths on the forming limits under complex strain paths are studied using this analysis. The predictions of the present analysis are compared, both for simple and complex strain paths, with experimental results of Ishigaki for A.K. steel and also with the predictions of Rao and Chaturvedi's model. The quantitative analysis of the error in predicting the forming limits has also been carried out using a method suggested by the authors earlier.1. INTRODUCTIONThe constant strain ratio condition has been assumed in the theories developed for prediction of forming limit diagrams (FLO). In actual forming operation, this condition is seldom satisfied. Even in the case of simple single stage press formed components, the strain path becomes curved and non-linear. In the case of pressings with complex shapes, or multiple stages of forming, the changes in strain path are more pronounced and even abrupt.Experimental study of the forming limits, under two stage strain paths, by Ishigaki [1], has shown that the forming limits are path dependent. It has been observed that the forming limits lower than that under simple strain paths, may be obtained under certain strain paths (when the first stage strain path is either equibiaxial tension or uniaxial tension, followed by the second stage strain path as plane strain). Rasmussen's work [2J, on the theoretical study of forming limits under curvilinear strains paths, has shown that a large drop in formability can result from very small changes in strain path. Thus if a deformation process gives rise to failures due to plastic instability, the failure is not necessarily due to insufficient formability of the material. In such cases, FLOs based on constant strain ratio path should not be used directly in predicting the success or failure of the forming operation. Thus the knowledge of forming limits under complex strain paths is of great importance to the interpretation of press-shop problems."

Jan 1, 1994

By Saad Elias Kaskah

"The Box-Behnken Design (BBD) is used to model the sacrificial Cathodic Protection System (SCPS) to find the factors effectiveness behaviour. For protection potential assessment the BBD receives (resistivity of environment, sacrificial anode alloy, distance between anode and cathode and surface area for the structure to be protected) as input and gives the protection potential as output. By applying BBD with their analysis tools we get many results. The important results which are the factors individual effectiveness on the sacrificial cathodic protection (SCP) process are the resistivity which has the greatest effect on the potential protection (rank=l) followed by sacrificial anode alloy type (rank=2), surface area for structure protected required (rank=3) and distance between anode and cathode (rank=4). The interaction of sacrificial anode alloy and cathode area {X2X4 ) has significant effect on CP process with the limits which are used in this work while the other factors interaction (X1X2, X1X3, X1X4,X2X3, X3X4 ) has insignificant effect on the limits which used in this work.IntroductionFor carbon steel in seawater the normal corrosion potential E '°""_is in the range -550 to -600 mV vs. Ag/AgCI [1]. The most effective method to overcome the corrosion is cathodic protection {CP) which represents a control method in the steel wall corrosion. Cathodic protection has been used in several areas including marine and underground structures, storage tanks, and pipelines [2]. Sacrificial anodes system generates protective current which depends upon the inherent potential difference between the anodes and the structure to be protected. If the structure is made of iron or steel, any metal that is more active in the electromotive force series can theoretically be used as anode material [3]. There are many factors influencing on cathodic protection like resistivity (NaCl content), chemical composition of sacrificial anode alloy, distance between anode and cathode, surface area of cathode, temperature, humidity, velocity of solution, dust, impurities, bacteria and etc .. The present work studied four factors: NaCl content, resistivity), chemical composition of sacrificial anode alloy, distance between anode and cathode, surface area of cathode) with different three levels of values for each one. Then this work will find the optimum value from the factors levels that tacked to investigated there influencing on sacrificial cathodic protection system."

Jan 1, 2013

By I. Kim, J. C. Choi, W. D. Cho

"The effect of yttrium addition on the oxidation behavior of Fe3Al intermetallic compound was investigated in the range of temperature 800 to 1100 °C in 0.2 atm 02 in terms of oxidation rate and oxide adhesion. The oxidation rate of alloys, Fe-14.3 wt% Al and Fe-14.1 wt% Al-0.3 wt% Y, was nearly identical and the parabolic rate constant calculated as a function of temperature is Kp=5128 exp[-39506(cal/mol)/RT] mg2/cm4 hr.Rapid cooling and ultrasonic stress tests were carried out to test adhesion of scale formed on the alloys. While the oxide layer formed on the Fe-Al alloy without Y was found to be fragile and detached easily during the tests, the oxide layer formed on the Fe-Al alloy containing Y was protective, dense, and adhesive. The following two mechanisms were proposed to explain the adhesion improvement of Ah03 formed on the Fe3Al containing yttrium : (1) the addition of yttrium decrease generation of growth stress in alumina scale because the preferential diffusion of yttrium through grain boundary in alumina scale prevent internal oxidation of Al, one of main causes of growth stress, and (2) the second phase formed on the oxide scales prevents crack propagation through the scales, leading to better mechanical stability of the oxide scales.IntroductionIron aluminides have attracted the attention of many researchers as a candidate for use at high temperature because of their excellent oxidation resistance due to the formation of protective alumina scale. In order to resist aggressive environments at elevated temperatures, oxide scale formed on iron-uluminum alloy must satisfy the following three requirements : (1) thermodynamic stability (2) slow growth rate (3) adherence on substrate. According to Wallwork and Hed [l], the most suitable alloys for high temperature application are Fe, Ni, and Co alloys with the protection of Si02, Cr203, and Ah03 scales. While chromium oxide can vaporize as Cr03 above 1000 °C and silicon oxide may form low melting silicate [2,3], Alz03 has a high melting point and is the most stable among the three oxides thermodynamically [6]. In this respect, iron aluminides forming alumina seem to be most suitable for use at high temperature. However, alumina scale formed on the iron aluminum alloys tends to be easily spalled during oxidation due to the combination of growth stress and thermal stress."

Jan 1, 1998

By Zhihe Dou, Yu Fang, Zimu Zhang, Yan Liu, Xiaoli Jiang Dianhua Zhang, Guanting Liu

"With the idea of “waste control by waste itself”, we come up with the crafts of using waste calcium carbide to mineralize CO2 in electrolytic aluminum waste gas, design and make out “Venturi gas-liquid-solid three stage reactor”, do experiments under the system of CO2-Ca(OH)2, investigate the influence on gas absorption by pH meter; investigate the influence on diameter distribution , rise velocity of bubble and local gas hold-up by dual conductivity probes; investigated the absorption of CO2 in every stage reactor under different initial proportion of CO2 by intelligent gas measurement system. The results showed that the reactor can fully absorb the CO2 in waste gas, and it has largely shorten the time of absorption and improve the CO2 utilization compared with the single stage reactor.The residual proportion of CO2 in the gas is below 0.08% through the absorption of three stage reactor,which show that absorption is extremely improved.IntroductionCarbide slag is a kind of polluting hydrolysis reaction byproducts in producing carbide in wet reactor, and it is mainly comprised by Ca(OH)2, It's estimated that there are about million tons carbide slag are piled up per year. Carbide slag is a kind of industrial wastes that hard to deal with ,which are treated by land filled in the past. It would not only occupy a lot of land, but also lead to secondary pollution [1].CO2 is the main greenhouse gas by now. In 2010, global CO2 emission has reached 33.5 billion tons, while China has now become the world's second largest emitter of CO2, emissions accounting for about one-seventh of the world [2].As the experts estimates, the greenhouse gas emission of whole nonferrous metal industry may over 0.6 billion tons per year, while CO2 emission of electrolytic aluminum is 0.334 billion tons per year [3]. So it is necessary and pressing to discover the reusing CO2 of electrolytic aluminum. With the idea of “waste control by waste itself”, we came up with the crafts of using carbide slag to mineralize the CO2 in electrolytic aluminum waste gas, which was experimented on the counterflow-three stage-venturi reactor,and studied the local gas holdup, residual concentration of CO2 and the volumetric transfer coefficient in the reactor."

Jan 1, 2014

By Z. Zhang, Zongshu Zou, Nan Wang

"Thermodynamic calculation is applied to make an investigation on the equilibrium phase relations and liquids of CaO-SiO2-Al2O3-FeOx system for different temperatures. The calculated results with FactSage6.1 show that the effect of temperature on the the equilibrium phase relations and liquidus of CaO-SiO2-Al2O3-FeOx system and its sub-systems is appreciable. The liquid phase regions enlarge with increasing temperature from 1573K to 1873K, while the primary phase fields reduce distinctly.IntroductionThe main oxide components of vitrified bottom ash slag are CaO, Al2O3, SiO2, Fe2O3, MgO, and Na2O, accounting for more than 90% of the bottom ash by weight[1]. During slag processing, the knowledge of thermodynamic properties and liquidus temperature in the related slag systems is highly required [2, 3], which is not yet available. Through literature survey [4-6], it is clear that the systematic information on the concerned complex slag system is scarce. So far the engineers in the field have to make assumptions of the thermodynamic properties of the simplified oxide system, without taking into consideration the interactions of the different oxide components, which hinders the development of the slag valorization and utilization. In order to provide thermodynamic properties for the application of the vitrified bottom ash, the six-component oxide system (CaO-MgO-Al2O3-SiO2-FeOx-Na2O) is highly required. A preliminary phase diagram of the CaO-MgO-Al2O3-SiO2-FeOx-Na2O system can be obtained from extrapolation of the thermodynamic functions of constituent subsystems such as CaO-SiO2-FeOx-MgO, CaO-SiO2-FeOx-Al2O3, CaO-SiO2-Na2O-MgO and CaO-SiO2-Na2O-Al2O3. In this work, the equilibrium phase relation and liquidus of CaO-SiO2-FeOx-Al2O3 system, one subsystem of the concerned complex slag system, are calculated and the effect of temperature is also discussed."

Jan 1, 2012