Search Documents

By G. P. Chaudhari, F. Warchomicka, M. Dikovits, V. Pancholi, C. Poletti

"The hot formability of a microalloyed steel with 0.16 wt-%C modified with N is studied by using processing maps. Compression tests of cylindrical samples are carried out using a Gleeble®3800 simulator in the range of temperature between 750 -1000°C and strain rates between 0.01-100 S-1. For this alloy, an Ar3-temperature about 740°C is determined by means of dilatometry. Processing maps are calculated using the modified dynamic material model developed by Murty and Rao for different logarithmic strains. For the instability map, the parameter Kj developed by the authors in previous works is used and compared with other instability values. Softening in the flow curves provoked by induced ferrite during deformation at low temperatures and low strain rates is reflected in the n-value. Light optical microscopy (LOM) and electron back scattered diffraction (EBSD) measurements are used to study the microstructure of the hot deformed samples to determine the deformation mechanisms active and to verify the processing maps.IntroductionProcessing maps offer a good possibility to optimize thermomechanical process parameters and to avoid defects in the products. Prasad et al. [1] developed the processing maps using the dynamic material model (DMM) and Murty & Rao [2] modified it. Processing maps consist of two superimposed maps: the dissipation efficiency and the instability map. The processing maps can be used to detect areas with a good hot formability, which are normally related to restoration of the material by dynamic recovery/recrystallization. For a high dissipation efficiency value and no instabilities, a good hot formability is predicted. In the DMM no storage of energy takes place and so the material is considered essentially dissipative, this is only true for high temperatures and high strain rates [1]."

Jan 1, 2012

By Chuan-fu Zhang

The fibrous precursor can be obtained by coordination precipitation process, using oxalate, cobalt chloride and ammonia. XRD pattern of precursor precipitated at pH=9.0 is different from that of ß-CoC2O4?2H2O precipitated at pH=1.0 which indicates that the precursor powders are one type of cobalt complex. According to the results of element analysis and IR spectra, it can be inferred that the composition of the precursor is [Co(NH3)x]C2O4?H2O(x=1.2?..6) formed by the coordination reaction at pH=9.00 in the Co(II)-C2O42--NH3-NH4+-H2O system. It?s found that the fibrous cobalt powders greatly inherited the morphologies of the precursors. Many factors could affect the formation of the fibrous cobalt precursor powders, such as the initial Co2+concentration, pH value and so on. The SEM images show how they influence the morphologies of the precursor powders. By adding proper surfactant, the dispersion of the precursor powders would be improved. At last, the final product-fibrous cobalt powders which are about 0.3~0.5min size and 40~60 in aspect ratio were produced by thermal decomposition of fibrous cobalt complex at 400~500°C in the weak reducing atmosphere.

Jan 1, 2006

By Qin Li

An highly active absorbent with oxidization based on fly ash, lime and additives was prepared. Experiments of simultaneous desulphurization and denitrification were carried out using fixture bed and duct injection. The influential factors for the absorptive capacity of the absorbent were studied. The absorptive capacities of 120.7mg for SO2 and 43.7 mg for NOx were achieved at a Ca/(S + N) molar ratio 1.2, respectively, corresponding removal efficiencies of 87% and 76%, while spent absorbent appeared in the form of dry powder. The optimal temperature and humidity of flue gas treated with this process were shown to be approximately 50\\176 and 5% respectively. The mechanism of removal for SO2 and NOx was investigated. In comparison with traditional dry FGD, this process appears to have lower cost, less complicated configuration and simpler disposal of used absorbent. The valuable references can be provided for industrial application by this process. The foreground of application will be vast in China and in the world.

Jan 1, 2006

By Michael D. Odekirk

The U.S. Bureau of Mines investigated solvent extraction methods for recovering scandium from water leach filtrates of sulfated tantalum tailings. These complex solutions typically contained 20 or more metals in significant quantities. Two commercially available organics, DEHPA and PC-88A, were identified as effective scandium extractants. The two organics were tested in continuous solvent extraction circuits to compare loading and stripping kinetics, recyclability, and general processibility. Results showed that 95 pct of the scandium, greater than 80 pct of the zirconium, and only small amounts of other solubilized metals were extracted. Scandium was stripped directly as a 3.6 pct Sc precipitate when a 3n NaOH liquor was used as the stripping agent. This precipitate was subsequently upgraded to 94 pct ScE3 via a selective HE leach.

Jan 1, 1993

By Richard Jack De Klerk

The standard industrial method of arsenic removal from acidic aqueous processing effluents involves coprecipitation of arsenic with ferric iron (Fe/As>3) by lime neutralization in continuous circuits. To better understand current industrial practice, continuous circuit coprecipitation experiments were performed to identify industrially relevant process parameters and co-ion solutes that contribute to improved arsenic removal and retention. The coprecipitated solids were subjected to accelerated ageing at 20°, 40° & 70°C and arsenic behavior was monitored and modeled. Staging and the presence of calcium ions were found to have the most significant impact on arsenic retention. In this paper the techniques used and major results obtained are discussed.

Jan 1, 2008

By Guangwei Wang, Changle Zheng, Yifan Chai, Jian Guo, Weiwei Geng, Jianliang Zhang

In this paper, characteristic and kinetics of CO2 reaction with four different kinds of coke such as top-loading coke, dry quenching tamping coke, wet quenching tamping coke and semi-coke were investigated based on isothermal method. Electric resistance reduction furnace was used to heat the sample. Volume Model (VM) and Shrinking Core Model (SCM) were used to calculate the kinetic parameters and to contrast with the experimental results. The results showed that the Volumetric Model (VM) was much suitable for the reaction of top-loading coke, dry quenching tamping coke and wet quenching tamping coke, while Shrinking Core Model (SCM) was much suitable for semi-coke.

Jan 1, 2015

By Zhang Qin

Dolomite is main impurity mineral in phosphate ores. In practice of phosphate ores production, the grade of concentrates is only containing P2O5 31-32%.In this study, even the increasing of floatation reagent consumption and decreasing of floatation recovery, economic performance is estimated high according to the decreasing of H2SO4 consumption in subsequent production of phosphate fertilizer and the increasing of products value. In floatation stage, influence factor include the synergism impacts of floatation collector, the stages, time, concentration of ore pulp, which were discussed respectively in this paper. Raw material is characterized by mineralogy, chemical analysis, the grain size analysis and milling test . The results show that the grade of concentration can reach to P2O5 36% by deeply de-magnesium oxide from phosphate ores by floatation , which yield a high added value.

Jan 1, 2009

By Feng Ningchuan, Guo Xueyi, Tian qinghua, Liang Sha

"In this study, copper adsorption by orange peel which was chemically treated with sodium hydroxide was investigated. The morphological and chemical characteristics of the adsorbent were evaluated by spectroscopy and N2-adsorption techniques. Equilibrium isotherms and kinetics were obtained and the effects of solutions pH, adsorbent concentrations and temperature were studied in batch experiments. Equilibrium was well described by Langmuir and Freundlich isotherms and kinetics was found to fit pseudo-second order type adsorptions kinetics. According to the Langmuir equation, the maximum adsorption capacities (qm) for Cu(II) was 50.25 mg·g-1 at pH 5.3. With the temperature increased from 16 to 60°C, copper removal decreased. The loaded adsorbent was regenerated using HCl solution and could be used repeatedly at five cycles with little loss of adsorption capacity. The results show additional chemical treatment of the adsorbent by NaOH, is favor of improving the adsorption capacity. Introduction Increased use of metals and chemicals in manufacture industries has resulted in generation of large quantities of effluent that contains high level of toxic heavy metals and it poses environmental-disposal problems due to its non-degradable, persistence nature and accumulation throughout the food chain [1, 2]. Copper is known to be a commonly used heavy metal. This metal, which found many useful applications in our life, is very harmful if charged into natural water resources and may pose finally a serious health hazard. Many methods, such as chemical precipitation, ion exchange, reverse osmosis and adsorption, etc., have been used for heavy metal ions removal from various aqueous solutions. In recent years, there has been considerable interests in use of biological materials including algae, bacteria, fungi, agricultural by-products and residues as adsorbents to remove toxic metals from aqueous solutions by adsorption [3-8]. Adsorption process has been extensively used to remove copper from aquatic medium using low cost adsorbents such as peanut husks [9], plant materials [10] and cellulose materials [11]. Among them, agricultural by-products and biomass are relatively cheap and show very high adsorption capacities. However, to apply untreated agricultural by-products as adsorbents has the disadvantages such as low adsorption capacity, high chemical oxygen demand (COD) and biological chemical demand (BOD) as well as total organic carbon (TOC), due to the release of soluble organic compounds contained in the plant materials such as lignin, tannin, pectin and cellulose, into the solutions [12-14]."

Jan 1, 2008

By Onuralp Yiicel, Ozlem Okur, Murat Alkan

"In this study, Co-Cr-Mo alloys were produced using a mixture of Co304, Cr203 and Mo03 powders with Al powders by a Self-propagating high temperature synthesis process. SHS is a process of material synthesis that has revealed a number of reactants combinations capable of much higher energy release than conventional explosives. Al203 is added to the mixture to decrease the adiabatic temperature of the system. The thermodynamic simulations and the calculations of adiabatic temperature were examined with FactSage 6.2. In the SHS experiments, different Co304/ Cr203/Mo03 ratios were examined, and their effects on the metal recovery and alloy compositions were carried out. The samples were characterized by using chemical analysis, XRD, XRF and SEM/EDS techniques.IntroductionSelf Propagating High Temperature Synthesis (SHS) has significant advantages compared to the high technology furnace applications, such as very short processing time, simple operation, low energy requirement and low cost [l, 2]. In a SHS process, the ignition starts the combustion and propagates throughout the reactant mixture yielding the desired product. However, the disadvantages of the process such as inhomogeneous or unreacted products due to undesirable reaction rates needs to be overcome by changing some parameters such as ignition temperature, particle size, additive, atmosphere etc. [3, 4]. This work aims to establish a scientific and engineering background in the production of some cast Co-Cr-Mo master alloys via SHS (Self Propagating High Temperature Synthesis) metallurgy which is attractive process technique regarding fast and low-cost production ability of cast alloys."

Jan 1, 2013

By Ning Wang, Bing Xie, Hong-Yi Li

"Compared to traditional sodium roasting, calcified roast inhibits chlorine pollution. A vanadium extraction technique based on a calcified roast is especially suitable for vanadium slag with high calcium content. In this report, V205was extracted from vanadium slag by calcified roast followed by acid leaching and hydrolysis precipitation. In optimized conditions, the high silicon low vanadium slag was roasted at 850'C for 2 hours without CaO addition. The roasted materials were leached with 35 % H2SO4 in liquid/solid ratio of 5:1 (mL/g) at 95OC for 4 hours. The extraction of vanadium was as high as 97.66 %. These results are instructive to V2O5 production in industry.IntroductionVanadium slag is produced in converter, sodium salt roasting is the commonly used technique to extract vanadium. In sodium salt roasting, vanadium slag is roasted with sodium salts including sodium chloride and soda as additives, followed by leaching with acidic or basic solution [1]. However, in this process chloride reacts to produce corrosive gases including HC1 andCl2- SO2 and SO3 can also corrode equipment severely and are also an environmental contaminant. The low melting point of sodium salts leads to fusion agglomeration, which blocks vanadium oxidation and thus decreases the extraction rate of vanadium. A large amount of sodium salts consumed as roasting additives increases the production cost. Moreover, sodium salt roasting requires low CaO content in vanadium slag. When the CaO content increases to 1%, V2O5 extraction can amount to 4.7%-9% [2]. For vanadium slag with high CaO content, the sodium salt roasting technique leads to low vanadium extraction rate."

Jan 1, 2012

By Damien Wagner

To reduce the emission of greenhouse gases by the steel industry, particularly for ironmaking, the production of DRI (Direct Reduced Iron) using hydrogen as the reducing gas instead of carbon monoxide is being considered. In this context, the reduction of pure hematite by hydrogen was studied at the laboratory scale, varying the experimental conditions and observing the rate and the course of the reaction. All the reduction experiments were performed in a thermobalance and supplementary characterization methods were used like scanning and transmission electron microscopy, X-ray diffraction, and Mössbauer spectrometry. The influence of rising temperature in the range 550-900°C is to accelerate the reaction; no slowing down was observed, contrary to some literature conclusions. A series of experiments consisted in interrupting the runs before complete conversion, thus enabling the characterization of partially reduced samples. Interpretation confirms the occurrence of three successive and rather separate reduction steps, through magnetite and wustite to iron, and illustrates a clear structural evolution of the samples. Finally, the influence of the sample type was revealed comparing a regular powder, a nanopowder and a sintered sample. The regular powder proved to be the most reactive despite its larger grain size, due to a more porous final structure.

Jan 1, 2006

By M. Nienoord, O. S. L. Bruinsma, J. A. F. M. Schade Van Westrum, W. H. Sillekens, B. Mehmetaj

Recycling of aluminium is an effective way of enhancing the efficient use of energy and limiting the burden on the environment. Where cascade recycling is an established way of using reclaimed aluminium, closing the recycling chain is currently hampered by the unavailability of suitable techniques for refining contaminated scrap on an industrial scale. To overcome this problem, purification based on fractional crystallisation appears to be a promising option. This implies that the material is to be processed in the semi-solid state; that is, at a temperature where a solid and a liquid phase co-exist. In the current paper, it is shown that zone melting can serve as an indi.cative test for assessing the refining potential of fractional crystallisation processes, since they are both based on the same thermodynamic principle. Next, the results of zone-melting experiments are presented for some representative aluminium model alloys. The BPS-model (developed by Burton, Prim and Stichter) is used to interpret these results, from which it is concluded that the model needs extension to obtain a predictive tool for fractional crystallisation processes.

Jan 1, 2000

By Matsufumi Takaya, Yukihiro Sakamoto

"Electric field emission properties from CVD diamond fabricated using pulse-modulated microwave plasma CVD were studied. Diamond was synthesized by microwave plasma CVD apparatus equipped with a pulse-modulated microwave power supply. Pulse conditions were varied from 1 to 10 seconds for pulse periods and from 0.1 to lHz for pulse frequency either. Surface morphologies of the deposits were differed by pulse frequency and duty cycle. As a result, FE properties prepared by different pulse duty cycle were different from continuous film which synthesized using continuous microwave significantly. Highest current density was obtained from the uneven morphology diamond film prepared at 17.5% pulse duty cycle.FE properties of the CVD diamond were depended on surface morphologies that related to the pulse conditions.1. IntroductionDiamond has excellent physical and chemical properties as an industrial material. Especially, hydrogen terminated diamond had the negative electron affinity (NEA) 1) and CVD diamond has this NEA property either as deposited 2). So the electron emission source to the FED is expected as one of this application of CVD diamond as cold cathode of electric devices. We studied on FE properties of various CVD diamond, pulse microwave plasma CVD diamond showed better property than those of other CVD diamond 3).This report studied on· the effect of the duty-cycle of pulse modulate microwave condition on FE properties of the diamond fabricated by pulse modulated microwave plasma CVD."

Jan 1, 2000

By Mark Samonds

"Manufacturing processes which involve liquid to solid and solid state transformations in metals encompass a wide variety of physical phenomena. The past twenty years have seen a steady evolution in the complexity and scope of numerical models of these processes, beginning with thermal analyses without phase change. Recently, a few software packages have become available which have true multi-physics capabilities. This permits the treatment of thermal, fluids, stress, electromagnetic, chemical reaction and microstructure development aspects altogether in a fully coupled simulation. This paper will consider various aspects of these types of models.Coupled thermal and fluid flow analyses of continuous castings have been around for fifteen years. Coupled thermal and free surface fluid flow simulations of shape castings have been available for ten years, including view factor radiation models for investment castings. Only recently, however, have fully coupled thermal, fluid, and stress analyses become practical. This implies the reverse coupling of the mechanical deformations to the solution of the energy and momentum equations through modification to the interface heat transfer coefficients and the fluid domain geometry. This has been implemented with a combined eulerian-lagrangian finite element method. Appropriate mechanical constitutive models will also be discussed.Many types of defects need to be predicted in casting processes. Those related to stress include hot tearing, hot cracking, part distortion, and thermal fatigue in dies. Macroporosity, microporosity, and microsegregation are determined by the solidification behavior and microstructure development in a casting. In particular, microporosity is influenced by dissolved gases, the morphology of the mushy zone, the liquid to solid density change, and the local pressure conditions. Macrosegregation is caused by the partitioning of solutes during. solidification and subsequent thermo-solutal convection. An additional transport equation is required for each solute that is being tracked. Computational thermodynamics is being incorporated into these types of analyses to determine transformation temperatures, partition coefficients, densities, and enthalpies. In combination, the microstructure and microporosity models can frequently predict a variety of mechanical models, such as yield strength, tensile strength, and elongation."

Jan 1, 2001

By Congcong Yang, Jian Pan, Deqing Zhu, Yang Zhong

A study of pelletization of one imported chromite concentrate with coarse site, poor ballability and refractory roasting performance was conducted in small scale tests, and high pressure grinding rollers (HPGR) was used to improve the pelletization. The mechanism of HPGR was revealed by means of SEM images and optical microscopy. Compared with the ball milling pretreatment, HPGR pretreatment can not only enhance the ballability of pellet feed but also drop the roasting temperature. Fired pellets, containing proper chemical compositions with high compressive strength of 2917N/pellet and good metallurgical performances, have been manufactured. The mechanism of HPGR reveals that chromite particle surface turns to more irregular after HPGR treatment and more new surface being formed because of more cracks, sharp corners and edges appearing, resulting in higher surface chemical activity, all of which improve the ballability of the chromite concentrate and contribute to the consolidation of fired pellets.

Jan 1, 2015

By Youn-Bae Kang

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

By V. I. Lakshmanan, R. Roy

"TiO2 is used in paints, plastics, rubber, paper, inks, textiles and other miscellaneous applications. The demand for the pigment grade Ti02 is growing at 3.0%/year on average and this invites the development of innovative and cost effective processes. The current processes are not designed to recycle the reagents and thereby discharge the effluents into the environment, causing an environmental concern.During this study, synthesis of TiO2 from an ilmenite concentrate was investigated using an innovative atmospheric mixed-chloride leach process. The solution purification was carried out using solvent extraction in two stages. In the first stage iron removal was carried out and in the second stage titanium was extracted. The strip solution obtained from the second stage solvent extraction contained the purified titanium and from this stream pigment grade Ti02 was recovered. The barren solution was used for reagent recovery and the regenerated leach liquor was recycled."

Jan 1, 2011

By Tim Robinson, Michael S. Moats, Masatsugu Moritmitsu, Kathryn C. Sole, Lauri Palmu, Frank K. Crundwell

"Process technology and design trends for copper, zinc, and nickel electrowinning cellhouses include focusing on energy reduction, productivity, and acid mist abatement. Larger electrodes, longer cells, automation, and higher current densities are leading to more capital-effective designs. The latest cellhouse designs include installation of automated electrode-handling systems, thereby removing more operators from the cellhouse. These technology and design trends result in lower electrowinning operating costs and improved purity of electro won cathode.INTRODUCTIONTechnology transfer between similar industries is an important process in improving product quality and productivity, and reducing operating costs. The electrowinning (EW) recovery of base metals, such as zinc, copper and nickel, is no different. The zinc industry with its larger EW product-handling requirements as compared to nickel and copper, has been driven to automation technology and the use of larger equipment. This technology has been transferred to copper. Nickel has led development and application in large-scale anode and divided-cell technologies but, due to nickel being produced in multiple forms (not just cathode) and being a small part of the whole complex nickel process route, the quantities of electrowon nickel are small compared to copper and zinc. Copper process technology in acid mist abatement was recently transferred to nickel. The focus in copper EW has been on energy reduction and productivity."

Jan 1, 2012

By Hiroyuki Matsuura

Treatment of electric arc furnace (EAF) dusts has become an important issue from the viewpoint of the environmental protection and recycling of variable resources because these dusts contain considerable amount of zinc and lead. A new recovery process of these metals has been proposed, in which the metals in the dusts react with waste polyvinyl chloride to form metal chlorides. Therefore, it is important to clarify the physicochemical properties and behaviors of zinc, lead and those chlorides and oxychlorides. In the present study, the kinetics of chlorination of ZnO, PbO and ZnFe2O4 mainly contained in the EAF dusts were investigated at 1023 K to 1273 K with Ar-O2-Cl2 gas. Based on these results, the selective chlorination and evaporation process of zinc and lead from the mixture of Fe2O3-ZnFe2O4-ZnO-PbO was examined and the high efficiency of selectivity has been demonstrated.

Jan 1, 2006

By Mariana H. Staia

Thermodynamic calculations based on the free energy minimization method were performed for the system Ti-Fe-Mn-0-C1-C in order to evaluate the chemistry associated with the chlorination of an ilmenitic concentrate using CCl4. In the calculations various weight ratios of FeTi03/ CC14, a , were considered, which varied between 0.32 to 0.98 at temperatures ranging from 673 K to 1273 K , at atmospheric pressure. The results obtained indicated that the operating conditions for a process in a packed bed reactor, which implies the chlorination of both Fe and Ti, are 0.39 < a < .49 at T 1173 K.

Jan 1, 1993