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By XING Xiangdong, Zhang Jianliang, MA Jinfang, WANG Zhenyang

The non-equilibrium reflux reaction behavior of phosphorus was studied with synthetic slags formed by using the AR chemical reagents and changing the initial condition of basicity, FeO, MgO and Al2O3. Due to increase of viscosity, the dephosphorization slag with high basicity inhibits the full contact of slag with iron, which leads to the low reaction rate in the early stage. However, since the high basicity improves the activity coefficient of CaO, the dephosphorization rate and phosphorus capacity goes up in late reaction stage. FeO promotes the increase of reaction rate in early dephosphorization stage. But the polarization force of Fe2+ is stronger than Ca2+, which hinders the reaction between phosphate ion and CaO and reduces the stability of PO4 3-. Thus, high content of FeO will adversely impact on dephosphorization reaction. In addition, MgO has a promoting effect to the dephosphorization, whereas Al2O3 has a negative influence.

Jan 1, 2016

By T. Malvik

Norway is a big producer of ferrosilicon and silicon metal. The raw material is quartz and quartzite and large quantities from both Norwegian and foreign sources are used. The demands maade on both the chemical purity and the thermomechanical qualities of the quartz/quartzite have increased in recent years in an attempt to reduce energy consumption and to improve utilization. Control of the chemical quality of the raw material is relatively easy by means of routine analysis, but it is more difficult to find a suitable method for testing the thermomechanical properties. A rapid test method to define high quality quartzite deposits for use in the metallurgical industry has been developed. The method is based on a combination of chemical analysis, dilatometry, thermosonimetry and cathodoluminiscence.

Jan 1, 1989

By Jingwei Lou, Bing Li, Suzhen Li, Miao Shen, Jianguo Yu

"As a main impurity in primary lithium metal, magnesium is difficult to remove because of the very close relative volatility of the two metals. Electrochemical refining provides a possibility to completely remove Mg in the LiCl-KCl melt prior to Li reduction. MgCl2 reduction processes in LiCl-KCl- MgCl2 melt were investigated by cyclic voltammetry (CV), square wave voltammetry (SWV), chronoamperometry and chronopotentiometry. Then potentiostatic electrolysis was carried out and Mg (II) ion was reduced onto a liquid lead cathode from the LiCl-KCl-MgCl2 melt at the Mg deposition potential. The results show that Mg ( II ) is reduced in one step with two-electron transfer. The reduction potential of Mg ( II ) was well defined. The reduction of Mg( II) results in Li ( I ) underpotential deposition at 0.2V more negative potential than that of Mg( II) reduction. Therefore, in order to prevent Li ( I ) from codeposition with Mg, accurately controlling Mg ( II) reduction potential during the potentiostatic electrolysis was necessary. Ninety three to 99 % removal rate of MgCl2 was achieved after 8-12 h electrolysis when liquid lead was used as cathode.IntroductionMetallic Li has been widely used in batteries, light weight alloys and in fusion reactors because of its excellent properties. Currently, the only way in industry to produce metallic Li is by electrowinning from molten LiCl-KCl at about 450 °C [l-5]. LiCl-KCl is the only electrolyte used, because they presents a lower eutectic temperature and KCl shows a slightly higher theoretical decomposition voltage than LiCl, as shown in Table l .The produced metallic Li generally contains 1-2 wt% impurities including Na, K, Al, Ca, Mg, Si, etc. [6l, which are derived from the corresponding metal chloride compounds or metal oxide compounds existing in the LiCl and/or KCl raw materials. These impurities have to be removed by subsequent vacuum distillation at high temperatures to meet the requirements for metal Li purity in the final products. Separation of Mg from Li by vacuum distillation is difficult because their relative volatilities are very close, as shown in Table 2."

Jan 1, 2011

By Hongmin Zhu, Guihua Wang, Xiangsheng Wang

"The anode process of carbon electrode in fluoride melt was studied by voltammetry and chronoamperometry. Anode gases were analyzed by gas chromatography on-line during controlled-potential electrolysis. Two peaks were observed on the cyclic voltammograms. According to the results of gas chromatography, the first peak was corresponded to the discharge of residual oxide ions, with the formation of CO and CO2. Discharge of fluoride ions occurred at 4.1 V vs. Li+/Li, and leading to the anode effect. With the occurrence of anode effect, small amount of CF4 was detected. As the potential reached 4.5 V, CF4 and C2F6 gas evolution occurred, and the current increased to form the second peak.1.IntroductionIn the primary production of Aluminum and some rare earth metals like neodymium, a departure from normal cell operation known as anode effect results in the generation of perfluorocarbons (PFCs), which have high global warming potentials [1]. Owing to the pressure of environmental protection, considerable research has been carried out to clarify the mechanism of anode effect and PFC generation of industry and laboratory cells in the aluminum electrolysis system [2-9]. The common result on PFC generation is that the PFCs are emitted from Hall-Heroult cells only when they are on anode effect. In this article, we selected LiF, the main electrolyte for the neodymium electrolysis [10-11], to perform further investigation on the underlying kinetics of PFC generation and the nature of the reactions at the electrode.2. ExperimentalAll experiments were carried out in an alumina tube reactor, which was filled with high purity helium atmosphere. Spectrographic graphite crucibles were used, which played the dual role of molten fluoride container and the counter electrode. Lithium fluoride was analytical grade. The experiments were carried out at 900 °C."

Jan 1, 2011

By Tian Tang, Sergio D. Felicelli

"The laser cladding is an important surface treatment for enhancing resistance against corrosion, abrasion, and wear. The focus of the present study is to develop a three dimensional finite element model to analyze the temperature history and thermal stress evolution during multi-pass laser cladding process on H13-H13 tool steel sample. A sequentially coupled thermal-stress analysis methodology was adopted in this study. The thermal model was firstly established to investigate the temperature history of the laser cladding process. Then the temperature history was used as input to mechanical model to calculate the thermal stress evolution during the process and the residual stress after the sample completely cooled down to room temperature. The influences of process parameters including the scanning speed and scanning strategies on temperature history, thermal stress evolution, and residual stress were investigated in details.IntroductionLaser cladding is an advanced material process technique, which is often used to improve mechanical properties or increase corrosion resistance, repair worn out parts, and fabricate metal matrix composites. In this process, the injected powder or wire feedstock material and a thin layer of substrate are melted and consolidated by use of a laser in order to coat part of a substrate or fabricate a near-net shape part.Numerous mathematical models have been established for analyzing the effects of process parameters, microstructure evolution, and thermo-mechanical behavior of laser cladding. Zhou et al. [1] established an analytical model to investigate the laser induction hybrid rapid cladding for Ni-based WC composite coatings. Huang et al. [2] also developed an analytical model to theoretically investigate the interaction between the laser beam and the powder stream of laser cladding process. A simple and realistic model of laser cladding was proposed by Picasso et al. [3]. The cladding layer is very sensitive to cracks due to the accumulation of residual stress, caused by non-uniform temperature changes, which have limited the wide application of laser cladding technique in industry. Recently, fmite element method has been increasingly used to simulate the laser cladding process [ 4-6]."

Jan 1, 2014

By Dachun Liu, Baoqiang Xu, Bin Yang, Yong Deng, Heng Xiong, Xiumin Chen

"In this paper, vacuum distillation technology has been employed to study the possibility and regularity of separating copper and enriching lead, silver and other valuable metals from copper- based multi component alloys. The result of experiment indicated the practicability of vacuum distillation dealing with copper base complex multi-component alloy to separating lead and silver, when the vacuum distillation temperature was 1637K, distillation time was 60min; residual gas pressure was 20-30Pa, the removal rate of silver was 95.86%, of lead was 99.63%; the evaporation rate of copper was 0.745%. The removal rate of arsenic, antimony and tin respectively were 83.09%, 48.12% and 24.54%. Vacuum distillation method is applicable for dealing with the copper-based multi component alloys, silver and lead can realize effective recovery.IntroductionCopper generally go with lead mineral, therefore, to remove copper from lead becomes an inevitable link in lead smelting. Dross from removed copper usually contains lead, arsenic, antimony, tin and noble metal silver. In abroad, soda ash-iron dust is adopted to process copper dross of this kind. The outcomes of this process are lead matte, wet lead, scoria smoke dust etc[1~5] The dominant components of all the outcomes are copper and lead. Moreover, in the process of tin smelting, copper contained by-products are produced, such as, crude tin alloy, tin lead electrolytic anode slime and so on. Copper content of all the products are ranging from few percentages to several tens percentage. Those products, no matter merge into main producing process, or separate treatment cost losses of valuable metal. For one hand, the containing of copper of outcomes from pyrogenic attack is less than 50%, for the other hand, a lot of valuable metal need to be processed, which increase the cost of retrieve."

Jan 1, 2013

By M. J. Bagshaw, J. D. Hunt, R. M. Jordan

"Continuous casting processes, and the roll casting process in particular, offer considerable potential to the Aluminium industry, both meatallurgically and economically.The three major limiting process problems that occur during roll casting are Centre Line Segregation', 'Sticking' where metal adheres to the rolls during casting, and 'Heat Line' formation. 'Heat Lines' are localised semi-continuous longitudinal defects, usually a few cms in width, where the cast metal leaves the roll bite partially molten. These defects occur at relatively low casting speeds when the mean slab exit temperature remains several hundred degrees below the solidus temperature. The objective of the work described here is to develop a better understanding of the roll casting process in general, and in particular, to understand the phenomenon of 'Heat Line' formation.A steady state two dimensional finite difference model has been developed to describe the roll casting process, incorporating a variable heat transfer coefficient through the roll bite. In the model the difference equations are formulated using a control volume method and latent heat is incorporated according to the Scheil equation. A Gauss-Seidel type technique is used to obtain the solution. Because the rate of heat evolution is non-linear the temperature in each box is determined by using a Newton-Raphson method. The solution for a box can be multi valued and therefore lead to instability particularly near the vicinity of the front. A stability 'criterion is presented which shows that to obtain a stable solution it is better to have long narrow boxes rather than boxes with small dimensions in both directions.The model explains why heat lines form in terms of the variable slab/roll heat transfer coefficient.Experimental measurements of slab exit temperatures are also presented. These were obtained on a Hunter twin roll caster for the binary AI-Cu system, at two compositions over as wide a range· of casting speeds as possible. The experimental results are compared with the predicted ones."

Jan 1, 1986

By Upali Siriwardane, Tushar V. Kudale, Naidu V. Seetala

"Cellulose acetate (CA) membranes with 25% triethyl citrate (TEC) as plasticizer were prepared with varying thickness for CO2 gas separation from water-gas-shift (WGS) reaction products. The AFM analysis of the CA membrane showed that the uniform coating had fewer and smaller pores as the film thickness increased, and corroborated by gas permeability studies. The CO2 permeability has decreased faster than CO permeability with the CA/TEC membrane thickness, and findings support that the CA membrane could be used to entrap CO2. Several CA/TEC membranes were also staked to increase the separation efficiency. Positron Annihilation Lifetime Spectroscopy (PALS) was used to estimate the nano-porosity (pore size and concentration) changes of CA/TEC films. PALS results show a decrease in pore size with increasing CA-TEC concentration in acetone, while the pore concentration increases. The PALS results are correlated with the CO2/CO permeability variations as the CA-TEC concentration change.IntroductionHydrogen is one of the main energy sources available for the future advancement of clean fuel technologies especially for fuel cells. Generation of hydrogen and CO2 from Water Gas Shift (WGS) reaction mixtures of CO and H2O is of interest to many researchers since it allows a large scale production of hydrogen [1, 2]. Once hydrogen is produced using the WGS reaction, the output products contain mixture of CO, CO2, H2, and water vapor. Metallic membranes have been used as hydrogen separation membranes [3-6]. As H2 is separated from the mixture using the metal membranes, we need to separate CO2, and find ways of sequestration of CO2 to avoid environmental problems by greenhouse gasses. Polymeric Membranes have been used for CO2 separation [7]. Plasticizer can control the micro-structural properties such as pore size and concentration of polymer membranes [8], which influence the size/molecular weight dependent diffusion rates of the gas molecules. We have used cellulose acetate with triethyl citrate as plasticizer to separate CO2 from the WGS reaction products. Positron annihilation lifetime spectroscopy (PALS) is very sensitive and able to identify different kinds of defects and their agglomerates such as vacancies, vacancy loops, and voids [9, 10]. PALS has been successful in determining the free volume in polymers that influence the properties of the polymers [11, 12]. Microscopic properties of the free volume obtained from PALS have been correlated to macroscopic properties [13, 14]. We used PALS to study the nanoporosity (pore size and concentration) and fractional free volume changes of CA/TEC films, and used to understand the variations observed in the CO2/CO permeability as the CA-TEC concentration in the membranes change."

Jan 1, 2014

By Miguel Barron

Recently, a new lance design for BOF steelmaking has been proposed in the literature. This lance, in addition to six peripheral inclined supersonic nozzles, contains a vertical centered nozzle whose oxygen flow is independent from the main oxygen supply. The above authors affirm that their lance maximizes the droplet generation without causing spitting. In this work, the performance of a lance with four peripheral nozzles and one vertical centered nozzle is numerically modeled by means of Computational Fluid Dynamics software. Transient two dimensional computer simulations were carried out considering two phases, namely molten steel and gaseous oxygen. Numerical results confirm that bath agitation and droplet generation are enhanced as a result of the vertical centered nozzle, however a proper performance of this lance, related to a conventional one, strongly depends on the Mach number of the oxygen jets and the lance height.

Jan 1, 2008

By Marcelo B. Mourão

The reduction of iron ores by solid carbon, when both are agglomerated together in the form of pellets, has important kinetic advantages. Although several studies have been performed on the subject, some points on the controlling mechanisms need clarification. There is a big scatter in the values of the apparent activation energy reported in the literature, and this may be due to factors like heat transfer, flow of gases in the reduction system, pellet size and composition. This work is concerned with the effect of several parameters on the reaction rate. The parameters studied were temperature (in the range 1173 K to 1423 K), carbon type (coke or charcoal), pellet size, gas flow rate, catalyst action of the produced metallic iron and added sodium carbonate. It has been shown that the values of the apparent activation energy can change according to the reduction conditions employed, and hence any modeling effort will have to take account of these parameters. EPD Congress 1994

Jan 1, 1994

By N. B. Gray, I. F. Taylor

"Gas injection to promote chemical reactions or mixing is a feature of many metallurgical processes. Often the aim of gas injection is to bring about a chemical reaction between the gas and liquid but most of the past physical and mathematical modelling work has ignored the influence of such reactions. In the work reported here, cold model studies have been conducted in which gas reacts with the liquid into which it was injected. The rate of liquid mixing has been measured as an indication of the mechanical energy transfer. It has been found that gas generated chemically within the liquid is significantly less effective at promoting mixing than the equivalent volume of inert gas. The relative ineffectiveness of chemically produced gas is thought to be due to smaller bubble sizes in comparison to the inert gas case. Small bubbles characteristic of chemically generated gas move with low slip velocities relative to the liquid and lead to different turbulence generation mechanisms.IntroductionIn processes such as steelmaking, copper conversion, bath smelting and ladle steel finishing gas is injected into liquid metal where it reacts chemically or simply serves as a source of agitation. An understanding of fluid flow phenomena in such situations is an essential pre-requisite to the calculation of process intensity and the optimisation of vessel productivity. Traditional physical cold modelling approaches to prediction of liquid flow in such situations are now often augmented by the techniques of computational fluid dynamics. Even with the availability of numerical modelling techniques cold physical models continue to have an important role for validation because it is generally difficult to obtain quantitative data from high temperature processes.Almost all previous cold modelling work has been based on the injection of an inert gas into water or some other non-reactive liquid. Such models do not include the significant increase in gas volume inherent in some processes. For example the oxidation of carbon in steelmaking leads to a twofold increase in molar gas flux through the reaction:"

Jan 1, 1996

By Masami Taguchi

"It is found that lead monoxide, PbO, has an ionic conductivity, and the all solid-state electrochemical cell using this oxide as an electrolyte has attracted the attention of battery researchers. In this study, thin film PbO2/PbO/Pb solid cells were produced on glass substrates and their discharge properties were investigated. The acti.ve material for the positive electrode, PbO2, was obtained by reactive sputtering of a Pb target in oxygen plasma. The PbO electrolyte and the active material for the negative electrode, Pb, were vacuum evaporated from /3 -PbO powder and a Pb block, respectively. The open-circuit voltage of the cell agreed with the theoretical value based on the thermodynamic data, and the close-circuit voltage was improved by the addition of a univalent impurity such as sodium or potassium to the PbO electrolyte. The connection of the cells in series and in parallel produced a higher electromotive force and a larger capacity. Also, the charge-discharge cycling test revealed that the cell could be charged and function as a storage battery.IntroductionGenerally, the ionic conductivity of a solid-state electrolyte is lower than that of a liquid electrolyte near room temperature. This has been a serious obstacle to using such electrolytes in an electrochemical cell. However, some solid-state electrolytes, which can preferentially pass a specified ion and have high ionic conductivity, have been found. Lead monoxide, PbO, which is an oxygen ion conductor, is such an example (1)(2). If a solid-state electrolyte is adopted for use in an electrochemical cell the problem associated with a liquid electrolyte such as leakage can be alleviated. The cell structure also can be simplified, because the electrolyte plays the role of separator to prevent the active materials from mixing. Thus, physical vapor deposition technology may make it possible to develop a very thin film cell, which consists of only solid phases (3)(4). In this study, the thin film PbO2/PbO/Pb solid cell with a thickness· of only a few micrometers, in which all the constituents were systematically deposited on a glass substrate by reactive sputtering and vacuum evaporation, has been produced and the charge-discharge properties were investigated. An attempt was made to improve the discharge properties by doping impurities such as Na2CO3 and Sb2O3 into the PbO electrolyte. Moreover, the connection of the cells in series and in parallel to get a higher electromotive force and a larger capacity, and the charge-discharge cycling test to determine its use as a storage battery were carried out."

Jan 1, 2000

By John E. Litz

Metal-bearing flue dusts are produced by some ferrous and non-ferrous industries. Many dusts are being or can be treated for recovery of metal values. Operating and proposed flowsheets for the most common dusts are reviewed. Advantages, disadvantages, product marketability, and cost implications are discussed for each flowsheet.

Jan 1, 1992

By Huang Kai

Uniform needle-like and spherical nickel oxalate particles were prepared by the chelating precipitation process, which was based on the reaction of oxalate acid and the solution of ammonia nickel chloride. The molar ratio of ammonia to nickel ion in the mixed solution is essential to determine whether the spherical or needle-like particles are formed, which means actually the concentration of ammonia is the key to determine the growth mechanism. When oxalate acid is added in the form of solid, it may act as the nucleation interface for the eariy-precipitated substance and so induce the formation of spherical particles. The PVP agent can improve the dispersing degree of the needle-like particles and higher reacting temperature leads to larger particles. The composition of the needle-like particle consists of ammonium and nickel oxalate instead of the pure nickel oxalate.

Jan 1, 2003

By R. Leiby

Prior to March 1992, the only component of the lead acid battery that was not recycled by East Penn Manufacturing Company was the sulfuric acid electrolyte. This acid was unusable in new batteries because the iron level was found to exceed new product specifications. The development of a liquid ion exchange process to remove the iron from the acid allows East Penn to currently recover over three million gallons of sulfuric acid annually. The process is based upon the use of an iron selective liquid ion exchange material or solvent to extract iron from the sulfuric acid electrolyte followed by regeneration of the solvent. Equilibrium and kinetic data for the extraction and regeneration steps were collected in order to scale up the process to commercial scale. An electrochemical process for the treatment of the acid used in the regeneration step was, also developed which significantly reduces the volume of strip acid required in the process.

Jan 1, 1995

By Derek J. Fray

The need for on-line sensors is outlined and it is demonstrated that the control of many processes is prevented by the availability of these devices. The use of solid electrolytes is described for the sensing of elements in molten pyrometallurgical phases. In the cases where there is no suitable electrolyte, the addition of a second phase of a compound containing both the element to be measured and the element whose ion is mobile in the electrolyte can be used. For the measurement of high concentrations of an element a method based on current measurement is proposed.

Jan 1, 1994

By Nico Steenekamp

At Lonrho Platinum in South Africa, ores from both the Merensky and UG2 reefs of the Bushveld Igneous complex are treated by flotation and smelting to produce a nickel-copper matte which serves as a collector for the platinum group metals (PGM' s). The nickel-copper matte was originally shipped to Norway for treatment and recovery of the contained base metals, with the return of the PGM rich concentrate to South Africa. The Lonrho Platinum Base Metal Refinery was commissioned in 1985. The original process employed a Shenitt Gordon design. The converter matte is treated in a refinery which utilises both atmospheric and pressure leaches for the dissolution of base metals to produce nickel sulphate crystals, copper cathode and a PGM concentrate. This paper refers to flowsheet and operating changes as well as improvements within the Base Metal Refinery.

Jan 1, 1999

By Dai Xi

In the present work, the viscosities of molten FenO-MgO-Si02 and FenO-MgO-CaO-Si02 semi-synthetic slags for nickel flash smelting were measured in the temperature range from 1473 to 1723K by a rotational viscometer. The ratio of Fe to Si02 was fixed at 1.2, calcium and magnesium oxide contents varied in the range from 2 to 8 mass% and 9 to 12 mass%, respectively. The results showed that silicate anions became smaller by increasing CaO content, which results in a decrease of the viscosity of the slag. In the case of MgO addition the viscosity behavior was complicated. At MgO content below 11 mass%, the viscosity increased with the increase of MgO at all temperatures tested. However, when the MgO content was above II mass%, the viscosity decreased slightly for FenO-MgO-CaO-Si02 system. At higher MgO contents, low-viscosity slags can be obtained by adding CaO. At a given composition, the viscosity decreased with increasing temperature. The higher the temperature, the more MgO can be added before saturation. The effect of Fe304 on the viscosity was quite significant. The viscosity of slag increased by 300mPa's at l573K when Fe304 content varied from 3 to 9 mass%. The viscosity values are presented as the functions of temperature and composition. A comparison between FenO-MgO-Si02 and FenO-MgO-CaO-Si02 systems is given in this study.

Jan 1, 2003

By H. Palkowski

Recent trends in the automotive industry lead to increasing interest in advanced high strength steels (AHSS). Those steels often have a high bake hardening potential (BH), giving additional contribution to the strength of structural parts, subjected to the paint baking process. For hot rolled AHSS, namely dual phase and martensitic steels, the effect of process conditions on mechanical properties had been investigated. However, the influence of chemical composition within the range in industrial production has not been investigated sufficiently yet. In the current research, samples with different chemical compositions within the characteristic interval for industrial production are under investigation under different preload conditions and simulating the thermo-mechanical production process. The samples were then subjected to BH process. Tensile tests were performed to study the influence of varying chemical composition on the BH effect. The results of investigations on dual phase steels will be presented in this paper.

Jan 1, 2008

By Dai Xi

In the present work, the viscosities of molten FenO-MgO-SiO2 and FenO-MgO-CaO-SiO2 semi-synthetic slags for nickel flash smelting were measured in the temperature range from 1473 to 1723K by a rotational viscometer. The ratio of Fe to Si02 was fixed at 1.2, calcium and magnesium oxide contents varied in the range from 2 to 8 mass% and 9 to 12 mass%, respectively. The results showed that silicate anions became smaller by increasing CaO content, which results in a decrease of the viscosity of the slag. In the case of MgO addition the viscosity behavior was complicated. At MgO content below II mass%, the viscosity increased with the increase of MgO at all temperatures tested. However, when the MgO content was above II mass%, the viscosity decreased slightly for FenO-MgO-CaO-SiO2 system. At higher MgO contents, low-viscosity slags can be obtained by adding CaO. At a given composition, .the viscosity decreased with increasing temperature. The higher the temperature, the more MgO can be added before saturation. The effect of Fe3O4 on the viscosity was quite significant. The viscosity of slag increased by 300mPa-s at 1573K when Fe3O4 content varied from 3 to 9 mass%. The viscosity values are presented as the functions of temperature and composition. A comparison between FenO-MgO-SiO2 and FenO-MgO-CaO-SiO2 systems is given in this study.

Jan 1, 2003