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By N. Mizutani, S. Harada, Z. Asaki, T. Tanabe

"The development of lead-free solders is urgent in view of environmental standpoints. In this -work the wettability of tin-bismuth- silver solders on copper was studied. Three kinds of fluxes were used. The wettability of conventional eutectic tin-lead .solder exhibited an excellent level over the other solders of tin-bismuth systems. Poor wettability of the tin-bismuth solders may be caused by the growth or dendritic copper-tin compounds at copper/solder interface, in contrast to the case of tin-lead'· solder. The wettability was improved by the addition· of silver in the solder. In this tin bismuth- silver system, silver was abnormally concentrated at the copper I solder interface even in the initial stage of contact. The wettability of the solder and the thickness of compound formed on the copper have a good correlation; the solder containing 2% silver exhibited the best wettability and the formation rate of copper-tin· compound on the copper was slowest.IntroductionSocial demand to avoid lead use in the industrial fields has been recently promoted· (1) because of the environmental protection of water resources. Especially the lead-bearing solders have been widely used in electronics and automobile products, and it is urgent to replace them with nontoxic materials (2)-(4). Thus the development of lead-free solders becomes an indispensable subject to the new generations and many works (5)(6) have already been carried out on the research and development of new solders. New lead-free solders are expected to have some requirements, for example, moderate melting temperature, proper strength and integrity, and lower prices, as compared with conventional solders. There have been already several alloy systems developed. Among ·these alloy systems, tin-bismuth binary or tin-bismuth-silver ternary alloys have great advantages such as having a wide range of soldering .temperature by controlling con:ipositions, though they have such disadvantages as ""lift-off"" (7)-(9): It is said, on the other hand, that a frequently overlooked property of solders, or one that is typically ignored by the research scientist as an ""issue"" for the manufacturing or product engineer, is wettability (10), although a ·work on the wettability has recently been published (11). In this Work, therefore, the authors selected Sn-Bi-Ag solders and focused mi the effect of Ag-addition to wettability of the solder."

Jan 1, 2000

By Suman Das, Justin J. Gambone, Rohan Bansal, Ranadip Acharya, Paul Cilino

"This paper focuses on generating a quantitative microstructure prediction model for Scanning Laser Epitaxy (SLE) process based on coupled flow-thermal modeling using Finite Volume method. SLE is a laser-based additive manufacturing process for the deposition of equiaxed, directionally solidified and single-crystal nickel superalloys through the melting of alloy powders onto superalloy substrates. In the current work, the detailed effects of natural and Marangoni convection on the flow field are studied and the results are analyzed in terms of the temperature gradient, vorticity parameter, melt pool dimensions and mushy region extent. The detailed property data of the processed superalloy and the laser scan path are incorporated in the model to predict the microstructure in realistic scenario. An optimization study is carried out to evaluate the critical parameter values at which the columnar-to-equiaxed and the oriented-tomisoriented transition take place. This work is sponsored by the Office of Naval Research through grant N00014-11-1-0670.IntroductionSLE is a laser-based additive manufacturing process for the creation of structures in equiaxed, directionally solidified and single-crystal nickel superalloys through the selective melting and resolidification of superalloy powders. In SLE, a tightly focused laser beam is guided by a highspeed galvanometer scanners allowing for tight control of the amount of energy being applied to the top of the powder bed, as well as the speed at which the melt pool moves across the substrate. Under the proper operating conditions and with sufficient substrate meltback, the solidification microstructure follows the morphology of the underlying substrate, allowing for directional and even SX growth.Several reports on the modeling aspects of laser cladding-based additive manufacturing approaches can be found in the literature. Approaches based on Finite Element Methods (FEM) and Finite Volume Methods (FVM) are employed for the thermal modeling of the system [1, 2]. Gaumann coupled the Columnar to Equiaxed Transition (CET) modeling with the Rosenthal solution in earlier work based on laser cladding [3]. Rappaz et. al. provided a detailed modeling of the microstructure/columnar orientation based on the solidification velocity and crystalline orientation [4]. This approach is based on the selection of the growth direction that closely follows the melt pool normal direction. Later on, substrate orientation is also taken into account [5, 6]."

Jan 1, 2013

By Ana P. Paiva, Marc F. Comella, Sandra S. Reis, Joao N. Reis, M. Soledade Santos

"In this work, the influence of the malonamide structure, acidity of the aqueous phase and diluent on the equilibrium interfacial tension (IT) of N,N'-dimethyl-N,N'-diphenylmalonamide (DMDPHMA) and N,N'-dimethyl-N,N'-dicyclohexylmalonamide (DMDCHMA) in 1,2- dichloroethane (1,2-DCE), and DMDCHMA in toluene, with aqueous HCl, were investigated. IT isotherms were determined using the Du N ouy ring method. Densities of the organic phases were determined, and used to screen solute-diluent interactions. Formation of third phases was never observed; furthermore, ITs increase with the phase separation period, constant values being obtained for separation periods larger than 1000 seconds. Each malonamide interfacial efficiency at the oil/water interface is interpreted in terms of malonamide basicity, diluent polarity and malonamide - hydrochloric acid- diluent interfacial interactions.IntroductionFor several years now, N,N'-tetrasubstituted malonamide derivatives have been extensively investigated as liquid-liquid extraction agents since they were first proposed as the organic components of the DIAMEX process, with the aim of advantageously replacing tributylphosphate in PUREX [1]. Therefore, a significant part of research studies with malonamides appearing in the literature deal with the extraction of major and minor actinides in real or simulated spent nuclear fuels in nitric acid solutions [2]. Under typical experimental process conditions, the tendency shown by some N,N'-tetrasubstituted malonamide derivatives to aggregate in the organic phase, leading in a few cases to the formation of undesirable third phases, has been remarked and consequently thoroughly investigated [3, 4]. The increasing use of chloride streams as hydrometallurgical aqueous feeds is becoming a reality, and this fact is obviously deeply founded on an extensive research carried out to recover value-adding metals from these media. Following this trend, a number of N,N'-tetrasubstituted malonamides have already been screened for the recovery of iron(III) [5, 6] and platinum-group metals [7] from hydrochloric acid solutions. The results obtained are quite promising either in terms of total metal ion recoveries or selectivity patterns achieved. The formation of a third phase when iron(III) was extracted by the tested N,N'-tetrasubstituted malonamide derivatives has never been observed under the adopted experimental conditions, and the extraction data collected would need to be reinterpreted accordingly if any aggregation phenomena involving the considered extraction systems were to take place."

Jan 1, 2011

By Victor Zavodinsky, Sergey Rogov

"Pseudo-potential fully relaxed total energy calculations are used to predict a hypothetical Si1-xCxO2 (x<0.5) compound formed from SiO2 ß -cristobalite by substitution of some SiO2 complexes by CO2 molecules. The simulation shows that the Si1-xCxO2 compound can be quasi stable if the CO2 content is less than fifty per cent. It is assumed that six-molecule Si6-nCnO12 (n=3) rings can play a role of nucleuses for formation of the Si1-xCxO2 compound from SiO2 and CO2 molecules. Thus, silicon dioxide can be considered as a possible solid store for gaseous CO2.IntroductionThe problem of increasing of CO2 in the Earth atmosphere is one of the main modern problems of mankind. One of conceivable ways to decrease the harmful value of CO2 is to convert a part of it to solid state. Iota et al. [1] reported a polymeric (quartz-like) phase of CO2 solid synthesized at high pressure (~40 GPa) and at high temperature (~1800 K). Shortly after this experimental work, Serra et al. [2] reported a total energy calculation of several possible phases of CO2 using plane wave pseudo-potential density functional theory. They concluded that there should be a transition from a molecular phase to a phase isostructural to SiO2 -quartz in the range of 35 to 60 GPa. The latest calculations by Dong et al. [3] have shown that the more favored solid CO2 phase is ß -cristobalite. Recently, Kume et al. [4] have demonstrated the polymerization of CO2 even at room temperature at high pressures up to 80 GPa. Transformations of gaseous CO2 to different solid phases were studied recently experimentally and theoretically [5-8]. The main obstacle for using synthesized CO2 solid as a solution for the CO2 problem is its pressure instability. However the SiO2 ß -cristobalite with the same structure is stable.The question is whether a silicon-oxide system in which a part of atoms of silicon is replaced by atoms of carbon will be stable? If the answer is positive, this system can be considered, in our opinion, as a possible store for CO2."

Jan 1, 2009

By T. Watanabe, T. Fujiwara, S-Wan Song, Y. Nakagawa, R. Teranishi, M. Yoshimura

"We have tried a new method to fabricate cobalt oxide films onto porous films directly by an electrodeposition method at low temperature. The porous substrate films (membrane-filters and paper) were placed between a LiOH solution and a CoSO4 solution and treated under electricalcurrents of ~1 mA/cm2 using carbon cathode and anode. Effects of temperatures, flow rates and electrical currents have been investigated. As a result, we found that the LiCoO2 films and Co3O4 films were successfully fabricated on paper and/or porous PTFE filters at 120 °C, while CoOOH films were deposited at 80 °C. Furthermore, LiCoO2 films did not cover whole the substrates, but was fabricated just over the anode. The chemical reactions of electrodeposition were also considered from these results.IntroductionRecent agreements on global environment require rapid progress of low energy and low waste processings for the fabrication of thin films that succeed to the mass production with the high consumption of the fossil fuels (such as physical vapor deposition°, chemical vapor deposition2), dip coating with firing3) etc.). The total energy consumption in aqueous systems should be the lowest among all these processing routes, because a much lager excess of energy is necessary to create melts, vapor, gas, or plasma than to form an aqueous solution at the same temperature4)The ""Soft Solution-Process"" (SSP) was one of the best concepts to realize the low energy and low waste fabrication of inorganic materials. 5) Generally speaking, SSP gives similar results to any other processing using fluids (such as vapor, gas plasma) and/or beam/vacuum processing. However, the total energy consumption of all these possessing routes should be the lowest in aqueous systems, because a much larger excess of energy is necessary to create melts, vapor, gas or plasma than to form an aqueous solution at the same temperature (Fig. 1). This idea can be easily demonstrated, using the simple example of BaTiO3. The energy diagram for the formation of BaTiO3 from various precursors is shown in reference 4. The driving forces (AG) for representative synthesis reaction of (1), (2), (3), (4) and(5) are 38, 727, 3685, 17 and —14kcal/mol, respectively at room temperature. 6' 7"

Jan 1, 2000

By Ying Li, Xuling Chen, Xiaohui Fan

"In the sintering process, the behavior and performance of iron ores is extremely complex. Different minerals have different sintering properties. In order to use iron ores rationally and effectively, multilevel fuzzy evaluation method is used to establish the comprehensive evaluation model of iron ores. Because of the relative independent characters of iron ores in sintering process, the characters can be divided into physical and chemical properties, granulation performance, and sintering properties, are divided, and together with iron ores prices as the first level index for judging, which are used as the second level index for judging. Using the analytic hierarchy process (AHP) to determine the weight of each index, which is used as the second level index. The relative membership matrix is determined by triangular membership function, the comprehensive evaluation model is established.IntroductionIn China, sintering is the main method for iron ores agglomeration. Sinter accounts for more than 80% of the blast furnace. Sinter production in the iron and steel enterprises in China plays an important role[l-2]. As the main raw material of iron ores sintering, the objectivity and integration of iron ores evaluation is essential. The iron ores evaluation methods include of metric ton price evaluation method, iron grade of a single iron ores sintering, acid-base balance method, composition assessment method and other methods which are based on the chemical composition and physical properties of iron ores to measure the quality of iron ores[3]. The high-temperature mineralization is an important process in sintering process, which affects the structure and mineral composition of the sinter, and has a close relationship with the quality of the sinter[ 4]. Therefore, in consideration of the physical and chemical properties, granulation properties, mineralization performance and sintering properties, the iron ores are evaluated by multi-level fuzzy comprehensive evaluation. The multi-level fuzzy comprehensive evaluation method makes a comprehensive evaluation, applying fuzzy transform principle and maximum membership degree principle, considering a number of factors related to the things which are evaluated. The method has lower requirements for the amount of data, and which integrates qualitative with quantitative judgment. It has a unique advantage to make up for the deficiencies of traditional evaluation methods. It also can comprehensively evaluate the iron ores in a relatively short period, reduce a lot of experiments, improve efficiency and guide the sinter production[5-6]."

Jan 1, 2013

By Jincheng Hu, Honggang Zhong, Qijie Zhai, Congsen Wu, Cheng Zhang, Jingzheng Ye

"The influence of cooling intensity on the solidification structure and ferrite phase content of a new duplex stainless steel (DSS) was investigated by using a thermal simulation setup for continuous casting. The results showed that the characteristics of the solidification structure were similar to their industrial scale manufactured slabs, including chill zone, colunmar zone and equiaxed zone. And austenite morphologies were mainly primary and secondary Widmanstatten sideplates as well as intragranular Widmanstatten plates. In addition, it revealed that the ferrite content increased with an increasing distance from the chill surface and decreased at colunmar to equiaxed transition (CET) position, then the value remained relatively stable at equiaxed zone. Furthermore, the ferrite content presented the same trend with the cooling intensity ranging from 100 mL/min to 2000 mL/min with the values just varying in a slight range.IntroductionThe duplex stainless steel (DSS) is the kind of steel that ferrite phase and austenite phase occupy about 50% respectively, or the content of the fewer phase has to be more than 30% [l]. The success of modem duplex stainless steels is to a large degree due to their higher strength than austenitic stainless steels, higher toughness than ferritic stainless steels, good weldability and high resistance to stress corrosion cracking as well [2,3]. The cost of stainless steel production continues to soar in recent years due to the increasingly higher price of Cr. In order to decrease the production cost, a new type of duplex stainless steel was developed by Bao steel [4]. This newly developed duplex stainless steel had low Cr content compared with 2205 DSS, and was expected to be applied into automobile industry. However, this type of steel was still in the initial stage of development, and the influence of continuous casting process on its solidification process and structure was still unclear, which needed to be studied further. Several works published in literature presented the effect of continuous casting conditions on duplex stainless steel (DSS) 2205, 2304 [5,6]. It was discussed that the cooling intensity in the chill-side had little efficient influence on the phase transformation. In this paper, the effect of cooling intensity on the solidification structure and ferrite volume fraction of this DSS at a given cooling rate was investigated."

Jan 1, 2014

By Bing Hu, Zhu-Cheng Huang, Guang-Bin Xia, Hu Peng, Hua Wang

"The temperature rising characteristics and reaction of the reduction of iron oxide pellets with anthracite fines were studied using a MW-L0316V microwave oven and Leica-DM-RXP polarizing microscope. The results show that iron oxide pellets and anthracite fines have good microwave absorbing properties, and high temperature and reducing atmosphere in a relatively short time for reduction of iron oxide pellets can be achieved. The reduction reaction, which follows the unreacted core model, is rapid and the metallization increases from 13.41% to 56.57% as the reduction end point temperature increases from 850oC to 950oC. The iron is formed, fine grain crystals of iron are transferred and the contraction of metal phase occurs firstly at the surface of pellets, which hinders the reduction reaction at the center of pellets. The rate of reduction reaction increases slowly as the reduction end point temperature increases from 950oC to 1050oC.IntroductionIron ore direct reduction can be divided into gas-based reduction and coal-based reduction. Owing to the effect of the resource and the related economic benefits [1, 2, 3, and 4], the development of gas-based direct reduction technology is restricted, but the development of coal-based direct reduction supported by the relevant industrial policy has very good prospects for application.As a source of clean energy, in China microwaves have been applied in many fields [5, 6, and 7]. Chen Jin studied the reduction of carbon pellets under microwaves, and has made some progress on reduction kinetics and reaction mechanisms. Other countries also have related research in this field [8 - 15], for example, Kotaro Ishizaki and Kazuhiro Nagata have done research on the reduction reaction of carbon magnetite heated by microwaves. The research shows that Fe3O4 is deoxidized to FeO at about 800oC, and FeO is deoxidized to Fe at 1000oC-1025oC. Due to the very good heat absorbing properties of iron oxide pellets and anthracite fines, the selective and rapid heating of microwaves can rapidly raise the temperature of pellets and anthracite, and the iron oxide pellets can be rapidly reduced. In order to provide enough theoretical basis for direct reduction by microwave heating, this paper studies the temperature rising characteristics, behavior of the reduction reaction and the changes of the iron oxide pellets and anthracite in the microwave field."

Jan 1, 2011

By Renxing Li, Yongyong Gong, Yufeng Cheng, Zhenxing Yin, Xin Cao, Qijie Zhai

"This paper investigated the refinement effect of pulse magneto-oscillation (PMO) on the solidification structures of medium carbon steel S45C in metal mould. The induction coil was positioned at the middle of ingot. The results showed that solidification structure of the treated ingots was remarkably modified with a transformation from well-developed dendritic structures to small dendritic structures or globular structures compared to the untreated ingot. The area fraction of modified microstructure regions reached more than 80 percent. A further experimental investigation had been done to understand the influence of refinement effect on the solidification structure under different mould size. Theoretical analysis demonstrated that the mechanism for the refinement of solidification structure was that PMO promoted nucleation near the mould walls and changed the interface temperature gradient and concentration gradient in liquid, eventually leading to a transition from the columnar crystals to the equiaxed crystals.IntroductionIn recent two decades, the electromagnetic processing of materials (EPM) has been widely used in many fields such as ironmaking, steelmaking, and solidification processing [1-6], where EPM can control melt flow, modify melt shape, reduce macro-segregation and refine microstructure. Pulse magneto-oscillation [7-9] (PMO), as a novel technique of EPM, has a remarkable effect on grain refinement and high potentiality to be used in industrial production. Compared with ultrasound refinement technique, PMO can be easily employed to metal solidification processing for long time in no contact with hot metal liquid by using a water-cooled coil. Another important advantage is that PMO needs smaller energy compared to pulsed magnetic field which needs a very high current to obtain a strong magnetic field to get a satisfactory effect. These advantages mentioned above are beneficial for industrial application, which make it potential to be widely used in future. Gong et al. [7] have studied the refinement effect of PMO on pure aluminum and find that PMO can significantly modify the solidification structure of pure aluminum. Li et al. [9] have reported the effect of temperature field on solidification structure under the influence of PMO. On the basis of these works, this paper has studied the effect of PMO on solidification process of medium carbon steel S45C in a metal mould, which can also provide some information for industrial application of this new technique."

Jan 1, 2012

By Emily Chen, Randolph Kirchain, Gabrielle Gaustad

"As prices and demand for aluminum metal have increased over the past few years, secondary production has begun to outpace primary aluminum production. However, while recycling of packaging and automotive scrap has continued to increase, aerospace secondary materials remain a largely untapped resource. Shredded or co-mingled aerospace scrap has a high degree of compositional uncertainty due to the prevalence of high copper and high zinc alloy series. Although it is clear that upgrading strategies enable increased usage of aerospace scrap, it is not clear that they would be economic or efficient. Previous studies by the authors have shown that modeling techniques, specifically chance-constrained optimization, provide the ability to evaluate upgrading options in terms of potential aerospace scrap utilization and production cost. Three specific cases are analyzed: a dismantled case, a sorted case, and a shredded or co-mingled case; sensitivity analysis of resulting compositional uncertainty is also presented.IntroductionAluminum recycling has a number of key environmental and economic benefits. Secondary recovery forestalls depletion of non-renewable resources and avoids the deleterious effects of extraction and winning (albeit by substituting some effects of its own). For most metals, the latter provides strong motivation for recycling; for light metals, like aluminum, the motivation is compelling[1]. Fortunately, as prices and demand for aluminum have increased greatly over recent years, secondary production has begun to outpace primary production (Figure 1). However, while the recycling rates of many aluminum products such as used beverage cans and cars have increased over this period, aerospace secondary materials remain a comparatively untapped resource.This untapped resource for scrap aluminum is a very large one; aluminum is the primary aircraft material comprising about 80% of a planes unladen weight[2]. It is used extensively for airframes, landing gear, engine components, propellers, and interior trim. A standard Boeing 747 jumbo jet, for example, contains approximately 75,000 kilograms of aluminum[2]. At an approximate rate of 300 per year, more than 6,000 civil aircraft are forecast to arrive at end-of-life in the next 20 years, potentially creating a large aerospace scrap market[3]. Many military aircraft are already available for possible scrap use, however, most are currently in storage at air force bases around the world[4]. The underutilization of these aerospace scrap materials indicates a lack of economic end-of-life options."

Jan 1, 2008

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 Jorge Alberto Soares Tenório, Denise Crocce Romano Espinosa, Viviane Tavares Moraes

"The development of mobile phone technology has increased the replacement of outdated equipments for more modern models, transforming disposal of such devices into a serious environmental problem. Recycling appears as an attractive alternative to minimize the environmental impact of disposing such large quantities. Recycling can be accomplished by treating the printed circuit boards of used mobile phones by using the same techniques used in ore treatments with hammer mill; magnetic separation, electrostatic separation and grain size range. Before performing the recycling process a PCB characterization was performed to identify the fraction with the higher metals concentration/content. This study demonstrated that the electrostatic separation was not the best metals concentration of PCB aiming the recycling, while the non-magnetic residue had presented a more significant metal concentration. Furthermore, after the magnetic separation was possible to separate the following metals: iron and nickel.IntroductionPortable electronic devices have gained increasing acceptance over the last decades. Mobile phones sales in Brazil, for instance, have reached 104 million in 2007, and 128 million in 2008. It is estimated that, around the world, 100 million mobiles are thrown away every year, either because of loss of functionality or because newer models are launched in the market [1,2, 3]. Printed circuit boards in mobile phones are made of many materials, with approximately 83% in weight being metals and fiber-glass, and the balance being plastics pl. Several metals can be recovered from the electronics waste, such as copper, tin, iron, lead, nickel, titanium, aluminium as well as some precious metals such as gold, silver and palladium [4, 5, 6, 7, 8]. Concurrent with the increasing world demand for copper, there average metal content in ores has been decreasing. Economically interesting copper mines used to have 4% metal content, whereas presently, such content is around 1%, i.e., for every 1 ton of ore extracted, only 10 kg are copper [9, 10]. Approximately 33% of printed circuit boards (PCBs) composition is copper, that is, for every 1 ton of PCBs waste, 330 kg are copper [1]. Research in recycling PCB waste focuses on mechanical, electrometallurgy, pyrometallurgical and hydrometallurgical processes [3, 8]. Collecting and recycling obsoletes electro-electronic equipments is very important these days, in order to, not just preserve the non renewable natural resources but also to keep the environment and the population safe from the pollution caused by the toxic materials and heavy metals present in this kind of waste."

Jan 1, 2011

By Jean-Louis Dirion, Guy Depelsenaire, Patrick Sharrock, Souhila Kribi, Ange Nzihou, Jocelyn Ramaroson

"This study assesses the Novosol® process, an emerging technology developed by Solvay to treat heavy metals from dredged sediments using phosphoric acid. The main goal is to convert toxic metal ions, such as Pb2+, Cd2+, Zn2+ and Cu2+ to insoluble metallic phosphates. The effectiveness of the treatment was evaluated by performing the chemical reaction in a tubular reactor, followed by convective drying and maturation of the treated sediment at ambient temperature and finally thermal destruction of the organic matter by calcinations (500°C-700°C). Selected variables (acid concentration, volume fraction of solids, flow rate, drying and calcination temperature and time) were investigated. Laboratory scale experiments were carried out with various combinations of these parameters. The influence of the quantity of acid and the temperature of calcinations on physical properties of the sediment and stabilization of the heavy metals are discussed. Introduction The French territory counts 525 000 km of rivers which transport each year on average 6 million m3 of sediments. Their deposit causes the silting of channels, rivers and lakes. This completely natural phenomenon is exacerbated by the introduction of industrial and urban wastes into the erosion and sedimentation process. This silting leads to clogging of rivers, with a reduction in their flow rates. Consecutively, other problems appear, such as flooding risks, decrease of biological purification capacity and associated loss of the biodiversity. The presence of toxic compounds (from industrial, household or agricultural origins) in the sediments worsens the situation, and requires curing to restore the natural environment and its function. The dredged sediments are either spread on agricultural land, land tipped, confined or sent for chemical or physical treatment [12]. The first research programmes on toxic sediments appeared at the end of the Eighties in the United States, in Canada, in the Netherlands and in Germany. Several techniques of treatment were developed for the sediments; these techniques can be used alone or in combination. These techniques include extraction and concentration of the pollutants: the pollutants are isolated from the sedimentary matrix and the sediment is decontaminated. In some cases of organic contaminations, the pollutants are destroyed by chemical oxidation or biodegradation and in other cases, the contaminated material is either stabilized (mixed with hydraulic binders), or destroyed (incineration) [14,15]. Phytoremediation by afforestation has also been reported [19]."

Jan 1, 2008

By Jean Igor Margem, Rômulo Loiola, Sergio N. Monteiro, Foluke S. de Assis, Frederico M. Margem

"Fibers extracted from the ramie plant have been traditionally used in textile and are now being considered as polymeric composite reinforcement owing to their superior strength. Recently the mechanical behavior of ramie fiber reinforced polyester composites was investigated but no significant improvement was found. Therefore, the objective of this work was to carry out a similar investigation by changing the type of polymeric matrix. Specimens with up to 30% in volume of ramie fibers incorporated into epoxy were bend-tested until fracture. The results showed a moderate improvement with a tendency of decreasing stress for higher amounts of ramie fibers due to the weak interface developed with the epoxy matrix.IntroductionThe engineering application of natural fibers extracted from cellulose-containing vegetables, also recognized as lignocellulosic fibers, is presently considered an environmentally correct alternative to replace more expensive, non recyclable and energy-intensive synthetic fibers [1-3]. In fact, composites reinforced with traditional fibers such as coconut, sisal, jute, hemp, etc ... are already on the market in substitution for common glass fiber automobile components [4-6]. Even less known fibers like curaua from the Amazon region are being industrially used [7]. Economical and environmental reasons sustain a promising future trend for natural fiber composites. In comparison with the less expensive glass fiber among energy-intensive synthetics, lignocellulosic fibers are approximately five times cheaper. For the current situation of our planet, natural fibers are regarded as ""green"" environmentally friendly materials. They are abundant, renewable, biodegradable, and recyclable, above all, neutral with respect to carbon dioxide emission, associated with global warming.Several relatively unknown lignocellulosic fibers such as piassava [8], sponge gourd [9], sugar cane bagasse [10], buriti [11] and ramie [12], with simple and limited applications, or just byproducts, are now being investigated for their potential as composite reinforcement. This could widen the offer of new lignocellulosic fibers for composite reinforcement. The banana fiber, in particular, has a tensile strength around 700 MPa [13], which is comparable to the strongest lignocellulosic fibers used as composite reinforcement.In addition to polyester, the epoxy is another relatively strong polymer used as composite matrix. Therefore, the objective of the present work was to assess the mechanical properties obtained by flexural test, for epoxy composites reinforced with different amounts of banana fibers."

Jan 1, 2013

By Shadia J. Ikhmayies

"Cadmium sulfide (CdS) in the form of thin films is an interesting material because it has a large variety of applications ranging from photovoltaic to luminescent devices. N-type CdS is usually used as a window layer in the heterojunction CdS/CdTe thin film solar cells. A review of the photoluminescence (PL) spectra ofn-type CdS thin films prepared by different techniques was performed. The effects of different dopants and impurities and the effects of temperature and deposition parameters on the PL spectra were discussed. Annealing in different atmospheres causes the changes in material structure and phase change from cubic to hexagonal phase which can be detected through the variations in the PL spectra. CdCh heat treatment improves the cystallinity of the films and enhances the exciton peaks and the green band in the PL spectra.IntroductionThin CdS films deserve attention because their expected gap emission lies very close to the highest sensitivity of the human eye. Thus, one might assume that thin CdS films are an appealing host for photonic devices [ l]. They have been used in a lot of applications including electronic and optoelectronic devices [2]. Thin films ofn-type CdS are widely used as a window layer in heterojunction solar cells such as CdS/CdTe solar cells. Doped and undoped CdS thin films can be obtained by different techniques such as; spray pyrolysis (SP) [3], chemical bath deposition (CBD) [2, 4], pulsed laser deposition [5, 6, 7], laser ablation [l], thermal evaporation [8].Several experimental techniques have been used in order to study semiconductor defects. In particular, photoluminescence (PL) has been shown as a powerful and sensitive tool in examining the crystal quality of polycrystalline thin films. PL can be used in the detection of defects which are radiative active. These defects can also act as traps in the transport of carriers [9]. The photoluminescence (PL) of thin film CdS is strongly influenced by the unbalanced stoichiometry, which is typical for CdS and is in general evoked by a Cd surplus. With increasing Cd content, the emission spectra move far below the gap to the red spectral range. Besides stoichiometry problems, independent of the material deposited, the PL properties of thin films depend on surface features and the influence of the interface between the film material and the substrate [10]."

Jan 1, 2013

By D. F. Liub, Z. Y. Liu, W. Y. Xue, Y. F. Shenb, Y. D. Wang

"The microstructure characteristics and deformation behavior of ultrafme grained (UFO) 304SS fabricated by accumulative rolling and armealing have been investigated by means of tensile tests, electron-backscatter-diffraction (EBSD) and transmission electron microscopy (TEM) techniques. The volume fraction of martensite phase decreases with increasing armealing temperature. In the grain sizes ranging from 300 nm to 10 µm, the strength held Hall-Petch relationship. The sample with an average grain size of 300 nm exhibited extra high yield strength of 1700 MPa and a tensile strength of 1780 MPa, while the elongation retains 12%. The limited uniform elongation in the UFO materials could be explained in terms of plastic instability. Very interestingly, for the bulk material with an average grain size of 1.200 µm, the high yield strength and uniform elongation were simultaneously achieved to be as 1000 MPa and 18%, respectively.IntroductionUltra-high strengths have been achieved in elemental metals by employing heavy plastic deformation, or by creating ultra-fine-grained (UFO) structure. Here UFO materials are defined as polycrystalline solids with property-controlling microstructural features below the 1 µm level. Typical processing routes include severe plastic deformation (SPD) [1, 2], which decomposes the grains through dislocation accumulation and reorganization (polygonization). Several different kinds of SPD process for bulk materials are typically as equal-charmel angular pressing (ECAP) [3], high-pressure torsion (HPT) [4] and accumulative roll-bonding (ARB) [5]. One of the main motivations for such a push for the very small grain sizes stems from the expectation of unprecedented mechanical strength, as predicted by the well-known Hall-Petch relationship that projects a continuous rise of strength with decreasing grain size [6]. However, these ultra-high strength metals no longer have the high ductility typical of their conventional coarse-grained counterparts, because the undesirable inhomogeneous deformation on the microstructure level can lead to the early onset of failure, severely limiting the useful ductility [2]. Recently, the interesting strategies have been performed to increasing simultaneously the ductility and strength ofUFG pure copper and nanostructured alloys by Zhao et al [7, 8]. In a pure copper, a high ductility has been achieved without sacrificing strength by introducing a high density of pre-existing twins and a large fraction of high-angle grain boundaries. Their encouraging results trigger our motivation to obtain high strength and ductility from the commercially bulk material."

Jan 1, 2013

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 Reuben John Mathew

"Oxygen evolution is the main anode reaction in industrial copper electrowinning. The oxygen bubbles do not conduct electricity, thus increasing the electrolyte resistance. The oxygen bubbles formed at the anode rise to the surface, occupying a larger volume of the electrolyte at the top of the cell than at the bottom. This oxygen bubble concentration gradient contributes to a gradient in electrolyte resistance and consequently a tendency toward uneven current distribution. This phenomenon increases the chance for uneven growth on the cathode and/or short-circuits, particularly on the lower portions of the cathode. This issue may be ameliorated by increasing the charge transfer resistance for oxygen evolution down the height of the anode. This concept was studied by solving the current distribution for a 2-D model of a copper electrowinning cell using COMSOL.IntroductionA copper electrowinning tankhouse aims to operate at the highest current density that will deposit on the cathode a layer of copper metal possessing the desired physical and chemical characteristics. The operating current density is directly related to the physical nature of the copper deposit on the cathode (Figure 1), limiting a copper electrowinning tankhouse to some operating current density that produces acceptable copper deposits.[!] The ratio of the operating current density to the limiting current density is typically around 0.3.[2] If the limiting current density for a cell could be raised, the operating current density could also be raised and thus result in savings in capital cost for a tankhouse. [3]The average operating current density in a copper electrowinning plant is 270A·m- 2 .[4] The value for average current density, however, obscures the fact that the face of a cathode does not experience this value equally. Indeed, the current density varies along the height of an electrode and is independent of the height of the electrode.[5] This phenomenon partly explains why the lower portions of a cathode tend to display a rougher copper deposit.In order to utilize a higher operating current density but still remain at 30% of the limiting current density, the limiting current density must be raised, but it is affected by the mass transfer regime at the electrodes. The mass transfer regime is currently poorest at the lower portions of the cathode and this is part of the reason for the tendency for poor cathode deposits to occur at the lower portion of the cathode.[6]"

Jan 1, 2012

By M. F. Hochella

Transmission electron microscopy (TEM) and energy dispersive X-ray (EDX) analysis have been used to study the mode of occurrence and mineral associations of gold in partially oxidized high grade gold ore from the Carlin sediment-hosted deposit. Rounded.gold particles have been observed that range in size from 0.03 to 0.1 p.m (300 to 1000 A) in diameter. The gold is associated with maghemite h-Fep3l and a K-Al-Si-bearing phase that is suspected to be illite. Detailed descriptions of gold and its mineral associations in &apos;Carlin-type&apos; gold deposits are critical not only to understanding the mechanism of fluid transport and precipitation of gold, but also to developing improved metallurgical techniques for the recovery of gold from refractory ore. Direct observation of gold in unoxidized ore is rare due to its relatively high degree of dissemination and low average bulk concentration which averages 9 ppm according to Radtke (1). Hausen and Kerr (2) observed 1 to 5 p.m grains of gold directly in oxidized ore but these microscopically visible particles account for only a small percentage of gold present in the ore. The samples used in this study were selected from individual beds of high grade, partially oxidized ore (4.55 oz/ton or 156 ppm gold) that were collected in the Main pit of the Carlin mine. The samples were collected from several thinly laminated carbonate micrite beds within the top 50 meters of the Roberts Mountains Formation. The carbonate micrite has been altered by hydrothermal fluids to a calcite-absent, moderately silicified rock referred to as alteration zone #3 by Bakken and Einaudi (3). Based on petrographic and SEM studies, the samples contain carbonaceous matter, and both pyrite and iron oxide pseudomorphs after pyrite. The oxidation of pyrite may be a pro-duct of deep weathering, in which case limited remobilization of gold may have occurred. TEM sections of the rock were prepared by first embedding small chips in low viscosity epoxy. The epoxy blocks were cut with a Reichert Ultracut E ultramicrotome, producing thin sections less than 0.1 p.m thick. The sections were examined with a Phil-lips 400ST TEM at 120 keV in both imaging and selected area diffraction modes. Native golci*was easily detected in TEM bright field images due to the large electron density contrast between gold and all other phases that are present (Figs. 1 and 2), Gold was positively identified with high spatial resolution EDX analysis in the transmission electron microscope, although selected area diffraction of individual grains was not successful EDX analyses of the platy and massive minerals immediately surrounding the gold particles typically indicate the presence of Si, AI, K, and Fe, However, the d-spacings derived from selected area diffraction of these polycrystalline masses (as, for example, in Fig. 2) give an exact match for maghemite. As a result, there is no diffraction information to identify the K-AI-Si-bearing phase(s). The lack of a diffraction pattern could be due to either electron beam damage or to a poorly crystalline phase(s).

Jan 1, 1987

By Xin-liang Gao, Qing Li, Gui-qin Fu, Duo Jin, Miao-yong Zhu

"Optical microscope together with alternative wet-dry cyclic accelerated corrosion tests and XRD, SEM were employed on bridge weathering steel samples with different Mn and Ni contents which were vacuum induction melted and rolled to study their effects on the microstructure and rust layer evolution in er' containing condition. The results show that the microstructure is mainly ferrite and pearlite when Mn and Ni contents are 0.75 %, 0.42 %, respectively. Both the increase of Mn and Ni contents will make pearlite disappear while granular bainite appear, meanwhile the grain size decreases. With the increase of Mn content, the corrosion rate decreases in the initial stage, but the effect becomes little in the later stage. The increase of Ni not only improves the corrosion resistance of steel base at the initial stage but also hinders the tendency of further corrosion. As Mn content increases, a-FeOOH contents in rust layer decreases. With increase of Ni content, the content of a-FeOOH in the rust increases while that ofy-FeOOH decreases.IntroductionWeathering steels had been ~radually applied in manufacture of bridges owing to reducing the corrosion rate remarkably [I- l .Good weldability was needed for high performance bridge weathering steels. Since carbon was thought to be bad for weldability, low carbon content steel was adopted and Mn was added to amend the mechanical strength loss. Some scholars[6, 7l believed that Mn was beneficial for increasing corrosion resistance performance of the steel in marine atmospheric environment. Some scholars [S, 9l thought that Mn had little effect on corrosion resistance in marine atmospheric environment. Presently, the effect of Mn on bridge weathering steel in marine atmospheric environment still remained poorly understood. Ni was considered to be beneficial for increasing corrosion resistance performance in marine atmospheric environment [JO-l4l However, the high cost limited its application range. What would bring to the rust and corrosion by decreasing Ni content needed further research.Most researchers assumed that microstructures only affected the corrosion behavior of bare steel. But the study of Guo et al. P5l showed that the homogenous microstructures were beneficial for the corrosion resistance of steels. The effect of Mn, Ni content change on microstructure and microstructure on corrosion still remained poorly understood. In the present work, the effect of Mn and Ni on the microstructures of steel matrix, as well as the microstructures on the rust and corrosion was investigated."

Jan 1, 2014