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By C. P. Broadbent

Due to growing .public awareness of environmental issues and greater sensitivity towards waste management, many countries around the world are implementing more stringent legislation governing the storage and disposal of hazardous wastes containing heavy metals such as As, Sb, Pb, Cd or Hg. These wastes can no longer be dumped without providing clear guarantees that the material concerned is environmentally safe and will not leach toxic elements to the surroundings. In the Netherlands the current dumping charge for chemical waste (i.e. worst category) is $280/t, and for industrial waste this cost reduces to $75/t. If the material can be reused there may be a small positive credit for selling it, for example discard slag as an aggregate to the construction industry. A number of (pyre)-metallurgical operations, mostly associated with the extraction of metals from sulphidic ores, produce arsenic residues in the form of As2O3 containing flue dusts and speises. If the flue dust is of high purity it can be sold, though many traditional uses are being substituted by other materials. In many cases upgrading the quality of the arsenical dusts is not possible for either technical or economic reasons. Traditional practice is to dissolve these dusts in acid prior to precipitation as ferric arsenate, which is at present classified by many countries as industrial waste and can be dumped. Recent work, however, has cast doubt on the stability of arsenates for disposal and alternative disposal routes have been investigated. Tests have shown that up to 10% (dm) As can be incorporated into "glassy" silicate slags with very low levels of arsenic leaching in the cooled product. Calcium arsenate was added to a range of synthetic and industrial slags from the system SiO2-FexOy-CaO-A12O3-AsmOn, under mildly oxidising conditions and quenched subsequently in water. It would appear that this represents an environmentally acceptable method for the disposal of many arsenical residues and there is some optimism that this method will be equally applicable to the disposal of other toxic metal residues.

Jan 1, 1994

By E. Salinas-Rodriguez, J. Hernández-Ávila, E. O. Ávila-Dávila, A. Romero-Serrano, M. Perez-Labra, G. Juárez-López

"Single phase rubidium jarosite was synthesized by precipitation from aqueous solution. X-ray diffraction and SEM-EDS analyses showed that the synthetic rubidium jarosite formed in subspherical particles with an average particle size of about 35 µm. The chemical analysis showed an approximate composition of Rbo9432Fe3(SO4)2 1245(OH)6. The decomposition behaviour of the jarosite in terms of solution pH was thermodynamically modeled using FACTSage by constructing the potential-pH diagram at 298.15 K. The E-pH diagram showed that the decomposition of jarosite leads to goethite (FeOOH) together with Rb+ and SO42- ions. The experimental decomposition of the Rb-jarosite was carried out in alkaline solutions with five different Ca(OH)2 concentrations. The decomposition process showed an ""induction period"" followed y a progressive conversion period where the Rb+ and SO42- ions formed in the aqueous solution. In contrast, calcium was incorporated in the solid residue and iron was transformed into amorphous ferrihydrite. The kinetic analysis showed that this process can be represented by the unreacted-core chemically controlled model. The reaction order with respect to Ca(OH)2 is 0.4342 and the calculated activation energy is 98.70 kJ mol-1. IntroductionJarosite type compounds are hydrous sulfate minerals containing alkalis and ferric ions, MFe3(SO4)2(OH)6, where M can be H3O+· Na+, K+, Rb+, Ag+, NH4 +, Tl+, ½ Pb2+ or ½ Hg2+. Jarosite-type compounds were formed by the natural ""in situ"" oxidation of pyritic ores leading to the replacement of the original iron sulfides and iron oxides (Dutrizac and Kaiman) [1]. The great interest in jarosites is due to its ability to eliminate or diminish the iron concentration of the acid leach solutions produced in the hydrometallurgical zinc process, with relatively low losses of divalent metals such as Zn2+, Cd2+, Cu2+ or Co . However, the losses of the metal values demand a careful study of the conditions under which the jarosite compounds are formed together with their chemical properties."

Jan 1, 2012

By Mokka N. Rao

In this experimental investigation, the principal operating parameters of the spirals HC 1870 and HG 8/7 are determined for the hydrogravimetric separation of the friable siliceous iron minerals of the Piar Distric, Venezuela. Mineralogical characterization including optical microscopy of feeding materials and the products after separation are presented. Comparative analysis is made of effectiveness of productivity between the two spirals.

Jan 1, 1999

By Jie Li, Thomas A. Rawdanowicz, W. J. Collis, S. Venkatraman, S. Iyer

"InSb being the lowest band gap. material amongst the 111-V semiconductors with low effective mass has long attracted research interest, due to its potential application in far infrared devices and for high speed circuit elements. In this paper, we report, for the first time, Te-doping of InSb on GaAs substrate using SnTe doping source with molecular beam epitaxy (MBE) technique and its electrical characterization. The undoped epilayers are n-type in the temperature range of 10 K to 300 K investigated. The room temperature (RT) mobility as high as 64,810 cm2/V·s (1.9x1016 cm-3) have been measured on a 4.8 µm thick epilayer. Sn Te doping at different doping levels were investigated. 5. 7 µm thick doped layers with RT carrier concentrations ranging from 2x1016 cm-3 to 3.2x1018 cm-3 with corresponding full width at half maximum (FWHM) of x-ray (400) rocking curve varying from 170-200 arc-seconds have been achieved. The Hall mobility of 20,000 cm2/V·s at 1.3xl018 cm-3 carrier concentration was obtained indicating that SnTe is a good candidate as source material for n-type doping of InSb.IntroductionThe thin films of InSb and InSb-based alloys have found considerable interest because of potential applications in III-V semiconductor-based infrared optoelectronic devices1• In addition, the advantage of the small effective mass and the consequent high mobility can be utilized in high frequency and high-speed circuit devices2 InSb can also be used in magnetoresistive sensors for position sensing3. Epitaxial InSb films grown by MBE may be doped n-type with Si or Sn, or with the group VI elements, namely, S, Se, or Te. Of the group VI elements, Te may be advantageous because of its relatively low vapor pressure. However, the vapor pressure is high enough to have sufficient memory effect during MBE growth. Hence different telluride compounds such as GaTe45, PbTe6 and Sb2Te37 have been used as the dopant source for Sb-based compounds. SnTe has also been used as a successful n-type dopant in the MBE growth ofGaSb8 But, to our knowledge, there is no report on the investigation of SnTe doping of InSb. In this paper, we report the first doping characteristics of SnTe in InSb layers grown on GaAs substrate."

Jan 1, 1998

By V. Ramachandran

Under the Resource Conservation and Recovery ACT (RCRA), generators of listed or characteristic hazardous wastes must find satisfactory means for disposal. of wastes. Initially, for many this meant landfills and deep-well injection. Until recently, mining and metallurgical by-products have largely been exempt from RCRA, but now are coming under its jurisdiction. With the increasing closures of landfills, companies in the U.S. such as electroplaters, miners, metallurgical plants and others are turning to recycling as an alternative to treat their wastes. While the cost of recycling has been challenging, the long-term economics prove attractive because recycling interrupts the cradle- to-grave responsibility for the waste generator. The present paper describes the recycling of hazardous wastes at ENCYCLE/TEXAS. Encycle extracts marketable metals from metal-bearing sludges and wastewater using hydrometallurgical processes borrowed from the mining and metallurgical industry.

Jan 1, 1994

By Truan-Sheng Lui, Li-Hui Chen, Hao-Wen Hsueh, Fei-Yi Hung

"Since Ag wires have similar hardness and bonding properties to Au wires, they can be applied in some pads. In the present study, the annealing effect (at 225°C~275°C for 30min) on the tensile mechanical properties of silver wires with f=23µm was investigated. In addition, the micro-structural characteristics and the mechanical properties before and after an electric flame-off (EFO) process were also studied. Experimental results indicate that with annealing temperatures of more than 250°C, the silver wires possessed a fully annealed structure, the tensile strength and the hardness decreased, and the elongation was raised significantly. Under the thermal effect of EFO, the necks of the Ag balls underwent recrystallization and grain growth was induced, and the annealed Ag wires had a shorter zone of HAZ (220µm). The bonding strength and the neck-strength of the Ag wires were more than 7gf and possessed excellent bonding properties.IntroductionThermosonic ball bonding is one of the preferred processes for electronic packaging to connect a semiconductor chip and a lead frame by a thin metal wire. At present, gold wire and copper wire are the preferred interconnect materials to bond with the aluminum metallized wafer pads [1, 2]. Since gold is expensive and the reliability of copper is poorer [3], the study of silver wire has attracted a lot of attention already. In addition, the inherent properties of high ductility and low hardness of silver as well as its workability effectiveness compared to gold, have made it a preferred alternative .[4, 5]"

Jan 1, 2012

By José Sancho, Julia Ayala, Purificación García, Begoña Fernández

"Electrofilter dust, a residue generated in the last stage of the Bayer process in the hydroxide aluminum calcination, was characterized to evaluate the alumina that was potentially extractable with sulfuric acid. The process studied aims to produce aluminum sulfate for water coagulant uses, taking advantage of the residues that accumulate in large quantities in the proximity of plants with difficult recycling for storage. Acid leaching is carried out at different concentrations of sulfuric acid, at different temperatures, pulp densities, and times, to dissolve gibbsite and transition aluminas. The result is an aluminum sulfate solution without iron and with commercial specifications.IntroductionElectrofilter dust is a residue generated in the last stage of the Bayer Process [1] in the hydroxide aluminium calcination. The residue is a mixture of alumina and hydrates which have not completed their calcination process.Electrofilter dust, composed by alpha alumina, gibbsite and transition aluminas [2] can be leached in an acid medium by putting most of the aluminium in solution; the remaining residue should be mainly andisolved alpha alumina. In many hydrometallurgical processes, sulphuric acid has been selected as the cheapest and the most effective leachant [3,4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15]The aim of this study is to determine the effect of temperature, acid concentration and pulp density on the sulphuric acid leaching of electrofilter fines for aluminium dissolution, in order to produce aluminium sulphate for water coagulant uses. This will provide a commercial product and at the same time eliminate the environmental problem created as a result of the storage of large quantities of electrofilter fines in the vicinity of the Bayer plant."

Jan 1, 2008

By R. Cameron

The growing use and acceptance of electric vehicles (EV), as evidenced by the record sales of over 750 thousand vehicles in 2016 and a current global EV stock of 2 million vehicles, is putting pressure on sourcing raw materials such as cobalt, and to a lesser extent, nickel. Global supply is poorly diversified, with 50– 60% of global cobalt production sourced solely from the Democratic Republic of Congo (DRC). One potential source for cobalt and nickel are low-grade nickeliferous pyrrhotite tailings, of which 50–100 million tonnes are present in the Sudbury area alone. This paper presents the extraction of cobalt and nickel from this material using a combination of flotation and bioleaching technologies. The findings of a high-level techno-economic analysis of the proposed processing flowsheet are presented.

By O. Nakai

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

Jan 1, 1999

By M. M. Sadawy

"The increased rate of exploitation of iron ores has resulted in a rapid depletion of high-grade iron ore deposits in Egypt. New iron reserves have to be discovered to secure the iron ore for steel production. This paper aims to study the characterization and magnetic separation of low grade Aswan iron ore. The results showed that Aswan iron ore is composed of oolitic hematite, goethite, quartz and kaolinite. The screen analysis indicated that Aswan iron ore had a uniform distribution of iron and silica in the different particle size fractions and there is no any particle size has high amount of iron or low content of silica. On the other hand the results of dry high intensity magnetic separation illustrated that this technique is not suitable for upgrading this ore.IntroductionIron is one of the common metals used in industry, as well as being the fundamental raw material used in iron-steel industry; products are wide spread even in daily uses. The total iron ore reserves of the world have been estimated as 3 70 billion tones; 160 billion tones is classified as economical, while 210 billion tones as potentially economical [1]. An estimated 98% of the iron ore exploited in the world is used in the manufacture of pig iron and steel, which are non-substitutable backbones of modem society. The rapid increase of world steel production over the last few years have required an equal increase in iron ore production, from 876.8 Mt in 2006 to 948.1 Mt in 2007 [2]. The increased rate of exploitation of iron ores has resulted in a rapid depletion of known high-grade iron ore deposits. This, in turn, has led to a dramatic increase of prices. In the absence of any major new discoveries of high-grade iron ore deposits, mining companies have turned to lower-grade materials to assess their beneficiation potential to expand their production base and beneficiation capacity, in order to satisfy future demand. Egypt is going to face shortage in iron production, consequently new iron reserves have to be discovered to secure the iron needed for the country [3]. Exploitation of low grade ores requires special equipments and techniques for recovery of minerals values. High gradient magnetic separators offer promise and great potential of application both technologically and economically in the processing of fine particles containing weakly or feebly paramagnetic components [4-6]. Within this existing framework, this research was initiated to assess the beneficiation potential of low-grade Aswan iron ore by high intensity magnetic separation."

Jan 1, 2013

By E. García-Ramos, P. Flores-Sánchez, E. G. Palacios, B. Zeifert, A. Romero-Serrano, M. Hallen-López

Chromium containing slags from stainless steelmaking may eventually be leached by acidic environments, therefore they should be treated before being stockpiled or land filled. In this work, synthetic slags were prepared and the effect of CaO/SiO2, Cr2O3, MgO and Al2O3 contents on the stability of the mineralogical species formed was analyzed. The morphology and composition of the slags were analyzed by XRD and SEM-EDS, whilst their chemical stability was evaluated by leaching with an aqueous acetic acid solution. It was found that CaCr2O4 and CaCrO4 are present in slags prepared with neither MgO nor Al2O3. The Al2O3-based slags mainly produced Ca2Al2SiO7 and the Cr(VI)-containing oxide complex Ca4Al6CrO16, whilst MgO-based slags produced MgCr2O4 as main mineralogical species. Additionally, Eh-pH diagrams for the Ca-Cr-H2O and Mg-Cr-H2O systems at 25 °C were constructed. The lowest Cr concentration levels in the leaching liquors corresponded to MgO-based slags owing to the stable binding of Cr in spinel with MgO. It was also observed in the Al2O3-based slags that increasing the slag basicity from 1 to 2 the leachability of the slags are notably increased.

Jan 1, 2008

By D. M. Fermino, C. G. Bastos Andrade, V. F. Justo, F. R. Valenzuela-Diaz, M. G. S. Valenzuela, C. Volzone

The present paper presents the study of light green smectite clay, from Paraiba, Brazil, submitted to mild acid attack under moderated conditions. Usually, clays are subjected to treatment with strong inorganic acids at temperatures near the boiling point and at high acid concentrations and then, widely used as bleaching agents. The treatment occurred under bellow boiling temperature and at short times of reaction (90°C, reaction times of 1, 6, 12, 18 and 24 hours in close reactor, concentration of the aqueous solution of hydrochloric acid 1.5 M, clay/acid solution ratio of 1g/10mL). The purpose of these attacks is to reduce the concentration of impurities providing color, with minimal change in the clay minerals structure, aiming at use in products of high value such as cosmetics and polymer/clay nanocomposites. The raw clay and the attacked samples were characterized by X-ray diffraction (XRD), cation exchange capacity (CEC), stereomicroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray detector (EDS).

Jan 1, 2015

By Wen-Ming Chien, Vamsi Krishna Kamisetty, Amrita Mishra, Ivan Gantan, Prathyusha Mekala, Dhanesh Chandra

"The phase equilibrium and characterization studies by using high temperature X-ray diffraction (XRD) and differential scanning calorimetric (DSC) methods have been performed for binary organic thermal energy storage materials. The organic thermal energy storage materials undergo a solid-solid state phase transition before melting which stores large amounts of thermal energy. Two materials [tris(hydroxymethyl)aminomethane(TRIS) and 2-Amino-2-methyl-l, 3- propanediol(AMPL)] were used for this study. Binary samples of AMPL-TRIS were prepared to perform high temperature XRD characterization and DSC studies and the binary AMPL-TRIS phase diagram was developed. The high temperature solid-state phases of AMPL and TRIS were characterized as a disordered BCC structure. It was found there is virtually no solubility of TRIS in AMPL or vice versa below -75 °C. The maximum solubility of TRIS in AMPL is 11% TRIS at 75 °C. The eutectoid transformation was shown at 19%TRIS-81%AMPL composition and at a temperature of 75°C. Lattice expansion calculations on single phase of TRIS and AMPL have been performed.IntroductionThermal energy storage materials can store a large amount of heat due to the presence of thermal transitions from the orientationally ordered to disordered phases occurring before melting. These molecules (such as amine and alcohol derivatives of neopentane) can reorient as a whole about the central carbon atom to form orientationally disordered crystals (ODIC) and their spherical shape makes them reorient relatively easier. Thermal energy storage materials are becoming increasingly important as a renewable energy resource. These molecules undergo large changes in enthalpies at solid-solid transitions. The presence of these compounds with large enthalpy changes are identified as potential thermal energy materials and some of die applications are solar cell systems [1-3]. Binary mixtures have been found as a way to adjust the transition properties in addition to pure compounds [4]. Tris(hydroxyrnethyl)aminomethane (TRIS, C(CH2OH)3NH2) and AMPL, CH3C(CH2OH)2NH2) are two important thermal energy storage materials."

Jan 1, 2012

By Eduard Ouerra, Nuo Jin

"The use of polytetrafluoroethylene, PTFE, as a solid sorbent for elemental sulfur during pressure oxidation of chalcopyrite was investigated. The effects of agitation, PTFE particle size and lingin sulfonate addition were evaluated using leaching conditions that were otherwise similar to those employed in the CESL process. The effects of these factors and their interactions on chalcopyrite oxidation are explained in terms of interfacial forces and solid-solid interactions. Using relatively fine PTFE powder with vigorous agitation resulted in about 100% copper extraction in less than 90 minutes without the need for grinding of the flotation concentrate.IntroductionThe extraction of copper from sulfide ores has always been dominated by the conventional pyrometallurgical smelting process. Though much effort has been made to develop various hydrometallurgical processing routes, smelting remains as the dominant process, treating approximately 80% of the chalcopyrite concentrates worldwide [1]. However, some of recently emerged techniques for treating chalcopyrite through hydrometallurgical routes are showing results that are competitive with smelting in terms of economical feasibility. Representative methods include: Activox Process, CESL Process, Anglo/UBC Process, High Temperature Pressure Oxidation, and Bio-Oxidation. Among these, the CESL processes operate at a medium temperature range (typically 140-150GC) and oxygen pressure of 100 psi, with chloride as a catalyst, and reportedly achieve copper extractions of about 95% with a light regrinding of flotation concentrate to a p95 of 45 ìðé [2]. In spite of this satisfactory extraction result, the leach residues contain significant amounts of conglomerates which contain a small amount of unreacted concentrate [2], The conglomerations are formed because the elemental sulfur generated is liquid and sticky (melting point of sulfur being 119°C), and has a tendency to wet the sulfide mineral surface, a fact which inhibits the oxidation of the minerals. The overall process chemistry of the CESL process may be summarized as follows [3]:"

Jan 1, 2012

By Henry Hu, Alfred Yu

"A numerical model has been developed to simulate heat and mass transfer phenomena occurring during a novel magnesium reduction process-the vertical retort technology. The model was based on the control - volume finite difference approach. Simulations were run to determine the effect of various processing parameters on magnesium reduction cycle time. The model predicted temperature distributions, heating curves, recovery ratio of magnesium, and total process times. The predictions were used to optimize the magnesium reduction process including dimensions of the retort, geometries of the reactant compounds, and productivities. The results indicate that the implementation of the optimized processing parameters significantly decreases the reduction time, and consequently increases the production rate as well as lowers the energy consumption.IntroductionMagnesium consumption has been growing considerably in the past decade [1]. Of the total magnesium production, 30% is produced by the thermal reduction (Pidgeon) process, and it is anticipated to be still the main technology for producing magnesium in future [2]. One of the advantages of the Pidgeon process is that it is capable of producing high purity magnesium demanded by both the automotive and aerospace industries. However, the inefficiency of heat and mass transfer taking place in the horizontal Pidgeon reduction process results in low productivity, high energy consumption, labor-intensive operation, large floor space and high capital investment. This limits the production scale of a horizontal Pidgeon reduction process [3].Vertical reduction processTo overcome the shortcomings of the horizontal magnesium reduction process, a novel vertical magnesium reduction process [3] for large-scale production has been developed, in which heat and mass transfer in the retort is enhanced. The new process shortens reduction time, reduces energy consumption and increases productivity. The vertical reduction system is comprised of a vertically-placed retort, a heating furnace and a vacuum system. A section of the vertical retort is illustrated in Figure 1. Since the retort is set vertically, instead of horizontally, the entire procedure of loading the reactants material in the new process is different from the one for the horizontal reduction process."

Jan 1, 2001

By M. A. Barron, D. Y. Medina, R. T. Hernandez, I. Hilerio

"Chromium Nitride (CrN) thin fihns were deposited on steel AISI 316 substrates with reactive magnetron sputtering method. CrN films were produced under two different conditions. In the first one, the substrate was heated by a d.c. source. At the second coating was applied a negative substrate bias voltage. X ray diffraction, quantitative energy dispersive and scanning electron microscope, were employed to characterize their phases, chemical composition and microstructure. Additionally microhardness was evaluated using a microhardness tester. The results show that the phase formation of CrN thin films in the first case (with temperature) is better. Both coatings presented homogeneous surface. Their compositions shows differences though that gases flow are same. In attention to their hardness, presents an increment if it's compared with hardness substrate.Nomenclature.P Ar =Argon gas pressure during coating.PN2 = Nitrogen gas pressure during coating.Ts = Substrate temperature during coating.T f = Coating melting temperature. (CrN = 1050°C).E=Potential difference.t =Coating time.P=Target power (Cr) in magnetron sputtering de.HV = Vickers hardness.F = Applied charge.d= Average length of longitude of the two diagonals (mm)Introduction.Wear causes losses in materials surface, generating that components of mechanical systems suffer irreversible changes in their properties, causing a faulty operation of the system. It is important to control their effects, measuring and interpreting their causes clearly."

Jan 1, 2013

By Bora Derin, Sertac Yazici, M. Seref Sonmez

"In this study, the recycling conditions of waste liquor obtained after the production of tungsten boride powder from calcium tungstate by self-propagating high temperature synthesis (SHS) and the following hydrochloric acid leaching were investigated in detail. Environmentally unfriendly and extremely acidic (pH~ -0.3) liquor consisting of calcium, magnesium, and boron ions was treated with 1 M sodium carbonate solution to precipitate magnesium carbonate and calcium carbonate phases. The obtained amorphous precipitates were heated up to the temperature of 400°C for re-crystallization. As a result, MgO, CaC03 and CaMg(C03)z phases were obtained, while sodium, boron, chlorine ions were remain in the solution. The present study is still in progress.IntroductionSelf-propagating high temperature synthesis (SHS) is one of the techniques used in the production of a variety of advanced ceramics, inter-metallic, organic and inorganic compounds, oxygen free single crystals, and polymers [ 1, 2]. The reaction becomes selfsustaining and propagates in the reactant mixture, after initiation in SHS process. SHS products may contain the mixture of several unwanted compounds and elements. Therefore following acidic leaching process may be needed to purify the target product. In the previous study, calcium tungstate (Ca W04), magnesium (Mg) and boric acid (B20 3) mixture were reacted to produce tungsten boride powder by SHS process according to the Reaction 1. Then, magnesium and calcium containing byproducts (i.e. MgO, Mg3B206 and Ca3B206) found in the SHS product were leached out by using concentrated hydrochloric acid (HCl) solution to obtain pure tungsten boride powder [3].Ca W04 + 0.5B203 + 4.5Mg = WB + 4.5Mg0 + Cao (1)After the leaching, filtrate solution consisting of different amounts of magnesium, calcium, and boron requires additional treatment for the environmentally acceptable disposal.Several works were carried out about magnesium precipitation conditions and kinetics from brines. Rabadzhieva et al. investigated the precipitation of Mg(OH)z from brines by using NaOH as well as caustic soda [ 4]. Turek ve Gnot investigated the precipitation efficiency of Mg(OH)z for the temperature range between 10-40°C, while the reaction was kinetically experimented by Alamdiri et al [5, 6]. Homogeneous precipitation of nesquehonite (MgC03.3H20) by the reaction of MgCli with (NH4)2C03 in supersaturated solutions and factors that influence the precipitation of MgC03.3H20, such as reaction temperature, initial concentration, stirring speed, titration speed, equilibration time, have been studied by Wang et al [7]. The precipitation of Mg(OH)z by calcium hydroxide from aqueous solutions was studied by Baird et al. [8]. Stratful et al. focused on conditions influencing the precipitation of magnesium ammonium phosphate from wastewaters [9]. 1031"

Jan 1, 2011

By C. B. Piazzarollo

Red Ceramic materials are widely used in Civil Construction in Tropical Countries. However, these materials have high porosity and low mechanical strength. Thus, in order to improve these properties, recycle mineral wastes was incorporated into clay from Campos - RJ, ornamental rock waste, from the gneisses cutting of Cachoeiro - ES, 150 km from Campos. After the addition of up 10% of waste in clay mass, ceramic pieces were produced and subjected to the tests of porosity (P) and flexural strength (FS). The test material contains 53.3% clay and 67% waste slit. The X-ray diffraction identified the presence of kaolinite, quartz and feldspar for the clay and, for the waste, quartz and orthoclase. The results of FS and P showed that the residue influenced, positively, the ceramic piece, with strength gains especially from 920º up to 960°C.

Jan 1, 2015

By Chengyi Ding, Xuewei Lv, Changyang Ji, Rende Zhang, Xiangwei Zheng

The fraction of liquid phase in sintered ore can be the most important factor to determine the sinter quality and yield in sintering process. The generation ability of liquid phase for mixture of iron ore powders is determined by basicity, roasting time, roasting temperature and chemical composition of iron ores. Five different iron ores were selected in this study and the dried powders of iron ore and CaO reagent (<200 mesh) were homogeneously mixed together at their required proportions, then 15g of the mixture was pressed under a pressure of 20MPa to make a cylindrical sample with a diameter of 20mm. The sintering temperature in this study was kept at 1280℃, the gas phase is air, the holding time was varied with its three levels of 5min,10min and 15min. After that, the sample was cooled under room temperature in the air, and the cooled sample was analyzed by using zeiss optical microscope. The mineral phase compositions were quantitatively determined with an open source image processing software, Image J whicn can calculate the fraction of liquid phase. Besides, the study on how to estimate the sintering behavior of the raw materials in different conditions by the theoretical calculation is of vital importance, and the development of this will greatly improve the sintering production. Factsage will be used to calculate the liquid phases formulation during the sintering. Comparing the experimental results and the theoretical calculation shows that the mass of liquid phase increases with increasing basicity during the sintering, besides, the mass of calcium ferrite increases with increasing basicity. The generation ability of liquid phase of iron ores can be predicted through the experiment verification.

Jan 1, 2015

By Wenbin Liu

A novel route for rapid synthesis of ultrafine WC-Co cemented carbides with homogeneous binder phase distribution is reported. The composite powder is produced by in situ reduction-carbonization reactions by using WO2.9, Co3O4 and carbon black as raw powders. The reaction equilibrium and phase stability are studied by thermodynamic calculations. The WC-Co composite powder is condensed by spark plasma sintering (SPS) to obtain the cemented carbides bulk. The sintering temperature is lower than that in the conventional sintering methods by 1500C, while the sintering time is remarkably reduced by 3-5 times. The high performances of the hardness and the fracture toughness are obtained. The experimental results confirm that the present processing scheme of in situ reduction-carbonization reactions and subsequent SPS sintering is an efficient way to prepare WC-Co cemented carbides, and is apparently superior to the conventional long-period techniques of preparing composite powder and cemented carbides bulk.

Jan 1, 2008