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By Hongbo Zhu, Kun Yang, Jingyan Jia, Jinhui Peng, Libo Zhang, Yi Xia

"Titanium dioxide is broadly considered as the most potential useful photocatalytic material. In this work, titanium dioxide was synthetized by microwave solid-state method and characterized by thermogravimetry-differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The result demonstrates that through microwave solid-state synthesis, we can obtain uniform size and anatase TiO2 photocatalyst, with the precursor being Ti(C2O4)2·2H2O. And its degradation kinetic parameter of MO can reach to 0.21232.IntroductionSince Fujishima and Honda found the photovoltaic property of titanium dioxide TiO2 [l], it has been widely used in the field of pollutant degradation, virus killer and environment protection [2-5]. Compared to other semiconductors, TiO2 has the advantage of low toxicity/cost, chemical stability, excellent photocatalytic activity, and long lifetime of electron/hole pairs, thus it is considered to be a most potential useful photocatalyst material [ 6]. Solid-state synthesis of oxide nanoparticle is a new method developed in recent years, which not only overcomes the shortcomings of easily aggregation existing in traditional hydrometallurgical process, but also fully demonstrates the unique technologic advantages of without solvents, high yield, easy control, less environmental pollution in solid-state reaction [7-11]. Researches show that the new method of microwave synthesis shows a lot of advantages such as fast reaction rate, efficient, high purity of product, uniform morphology, energy-efficient, and nonpolluting [12-15].In this work, we associated microwave heating and solid-state synthesis to prepare TiO2 photocatalyst material. Its photocatalytic activity was studied in the degradation of MO queous solution. Meanwhile, the formation process as well as the crystal structure and morphology of the synthesized powders were characterized by means of chermogravimetrydifferential scanning calorimetry (TG-DSC), X-ray diffractometry (XRD) and scanning electron microscopy (SEM) techniques."

Jan 1, 2014

By Sergey Komarov, Manuela Diaz, Sano. Masamichi

"Mixing time, bubble behavior and absorption rate of gas injected into a liquid bath through rotary L-shaped lances have been studied by cold models with an effort to improve refining characteristics of metallurgical processes. Two kinds of the rotary lances were tested, namely the single-hole lance and the multi-hole lance. The effects of gas flow rate, bath depth and rotation speed were examined.It is found that when gas is injected through the rotary lances, the mixing intensity and the gas absorption rate are larger than that for the gas injection through stationary lances. The effect of rotation speed decreases as the bath depth and the gas flow rate increase.The multi-hole lance produces much smaller bubbles, which lead to an increase in the volumetric mass transfer coefficient by 3-4 times as compared with the single-hole lance. However, the effect of rotation speed is smaller for the multi-hole lance. The obtained results are explained in terms of the bubble coalescence and fragmentation, the rate of which depends on the departure bubble size and the power supplied to the liquid bath.IntroductionIn recent years, there has been a growing interest in the development of gas injector for metallurgical processes. The majority of the previous work was focused on modification to the injector design to improve mixing and to increase the of chemical reaction rate. These two goals can not be necessarily achieved by the same way. Bottom nozzles and stationary immersed top lances, which have been widely applied to steelmaking processes, are effective for the bath mixing, but have a limit to decrease in the bubble size. This results from a vigorous coalescence occurring between the bubbles when they rise in the molten bath as a bubble swarm.One of the ways to ensure the small bubble size and the effective bath stirring is the gas purging through rotary injectors. A number of studies have been undertaken to improve the refining characteristics by using rotary injectors. All of them are related to aluminum refining. The SNIF equipment (The Spinning Nozzle Inert Flotation) has significantly improved the quality of aluminum products at National Luxemburg Aluminum [1]. Rotary injectors made in the form of a disc have been applied to the Alcoa 622 [2] and the GBF processes [3]. A study of the gas injection by a rotary impeller has been carried out by C. Leroy and G. Pignacelt [4]. All researchers note the significant improvement in removal of sodium, calcium, hydrogen and non-metallic inclusion."

Jan 1, 1996

By Dilek Kirgöz, Onuralp Yücel, Murat Alkan

"In this study, Mo containing Fe-based alloys, such as Fe-Ni-Cr-Mo, were synthesized using a mixture of Fe203-NiO-Cr203-Mo03 powders reducing with Al powders by metallothermic process which is a high energy efficient, fast and low-cost production technique for synthesis of cast alloys and advanced ceramics. Detailed thermochemical studies were simulated by using FactSage 6.2 Thermochemical software in order to calculate adiabatic temperature of the reactions and effects of initial molar composition on the final products. In the metallothermic processes, effects of stoichiometric Al addition and addition of the oxide powders (Alz03, Si02, CaO, MgO) on the metal recovery and compositions of final alloys were carried out. Final products were characterized by using chemical analysis (AAS), 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 Fe based alloys (Fe-Ni-Cr-Mo) which are used as surface coatings, wear-corrosion-oxidation resistive applications 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 Fu-Shen Zhang, Mengjun Chen, Jianxin Zhu

"In the present study, different types of cathode ray tube (CRT) glasses were examined by sequential extraction combined with TCLP to provide possible explanations for how Pb and Ba leach out from the waste CRT glasses and to give possible reasons for why they leach out. Sequential extraction results showed that Pb and Ba in the CRT glasses dominanfly presented as the residual fraction. The exchangeable fractions of Pb and Ba were extremely low, less than 0.01 % of the total content, but they were higher than those required by the regulation limits, 5 and 100 mg/L for Pb and Ba, respectively. TCLP tests of the original CRT glasses and CRT glasses residues after each step of sequential extraction demonstrated that the extremely high leaching toxicity of CRT glasses mainly caused by its exchangeable and carbonate fractions of Pb and Ba.IntroductionIn recent years, the amount of cathode ray tube (CRT) contained monitors or TV sets in the market were sharply reduced, since they were substituted by novel and better electronic and electric equipments such as LCD and PDP, leaving huge amount of end-of-life CRTs. 50-85% of the total weight of this kind of computer monitor or a TV set is glass[1,2], which was classified to three categories according to their chemical compositions: black & white glass (BW), color panel glass (CP) and color funnel glass (CF)[3]. In order to provide shielding from X-rays generated during the picture projection process, lead, barium and strontium oxides were used in the glass. In general, a color CRT contains 1.6-3.2 kg of lead . Therefore, these glasses have attracted wide and tense attention due to the potential risk to the environment and human health."

Jan 1, 2011

By Dae Jin Ha

Sticking phenomenon occurring during hot rolling of two STS 430JlL ferritic stainless steels was analyzed by hot-rolling simulation tests. The sticking started from the initial nucleation stage in which the rolled materials were stuck onto the roll specimen surface, proceeded to the growth stage in which stuck fragments grew further, and reached the saturation stage. The modified 430JlL steel had a smaller number of sticking nucleation sites and slower growth rate than the conventional 430JlL steel because of higher high temperature hardness, thereby leading to less serious sticking. When the simulation test was conducted at 1070 °c, Cr oxides were formed on the surface of the rolled materials, and thus the sticking was drastically reduced because of the increased surface hardness of the rolled materials. In order to prevent the sticking, high-temperature properties of the rolled materials should be enhanced when rolled at 900°C or 1000 °C, and rolling conditions and alloying compositions, under which the oxide formation was promoted, were more important than high-temperature properties when rolled at higher temperatures than 1000 oC.

Jan 1, 2008

By Dinabandhu Ghosh

The stability diagram of the ternary system Ti-C-O is drawn in the present work for four temperatures, 1473 K, 1573 K, 1673 K and 1873 K, showing the stability fields of TiC, Ti, TiO, Ti2O3 and TiO2. An analysis of the system reveals that it is not possible to produce Ti in a carbon-saturated system; instead, the stable product is TiC. However, Ti can be an equilibrium product in a carbon-unsaturated system at prohibitively low values of pCO and pCO2; for example, at 1873 K, these limiting values are: pCO = 10-6.76 atm and pCO2 = 10-13.36 atm, which, when exceeded, produce TiC and TiO respectively. The magnesiothermic reduction is examined through the stability diagram (log pO2 vs. 1/T) of the system Ti-Mg-O, drawn for a number of pMg values, presenting the pairwise stability fields such as Mg(l) + Ti(s), Mg(v) + Ti(s), MgO(s) + Ti(s), etc. The diagram shows that magnesium reduction of TiO to Ti is possible only at T < 1641 K with pMg = 1 atm and only at T < 1569 K with pMg = 0.5 atm. An experimental scheme for Mg vapor reduction of TiO2 is proposed in which an argon stream is passed over a Mg(liquid) evaporator at temperature T1 (say, 1234 K); the resulting Ar-Mg mixture at 1 atm is subsequently flown over a bed of TiO2 at temperature T2. A thermodynamic analysis establishes that complete reduction to Ti is possible and that the best results are obtained when T1 = T2.

Jan 1, 2006

By A. Pagliero

The coulombimetric reduction method has been used as an evaluation technique for Pb-Ca-Sn anode corrosion in the LIX-SX-EW process. The proposed methodology involves three consecutive steps, i.e., cleaning, oxidation and reduction. They are carried out in the same experimental unit, in solutions containing 180 g/L H2S04 with and without the addition of cobalt. The authors have worked in a wide range of oxidation current densities, from 150 to 500 A/m2 for in a period from 0.5 to 120 hours. It can be concluded from the results that there would be a linear relationship between the applied electrical charge I*T (Coulomb) and the anode corrosion expressed as transformed Pb mass (mg), for solutions with or without the addition of cobalt. The exception is that for the last one the corrosion rate is 5 times faster, which was observed for every layer. From the evaluation of different corrosion layers, one can point out that its composition is mainly in the form of sulphate. In the presence of cobalt, about 67% of Pb would be as sulphate (PbSO4), about 27% as a basic oxide (PbO) and only 6% as oxide PbO2 on the surface. From this result, it appears that great transformations occurred in the metal/sulphate interface. Without the addition of cobalt, the proportion of oxide Pb02 on the surface increased up to 11.5%. According to the previous statement and considering that Pb was found mainly as sulphate, the authors recommend its determination be used as quality selection criterion. Its evaluation should be performed in the acid solutions with 200 ppm cobalt addition at an oxidation current density of 300 A/m2 for a period of 24 hours.

Jan 1, 1999

By Kimio Itagaki

The distribution behaviours of the VA elements between the gas, slag and matte phases in copper smelting were evaluated on the basis of the thermodynamic data, most of which were determined by the authors. The distribution is basically dependent on the process factors such as temperature, the content of the element in charge, the amount of the waste gas and degree of vapour saturation with the elements. The thermodynamic quantities such as the activity coefficients of the VA elements in matte, the activities of iron and copper, SO2 or 02 potential and the distribution ratio of the elements between the slag and matte phases seriously affect the distribution, and the behaviours in various smelters could be explained systematically and reasonably by considering the changes in these quantities, In oxidation smelting at PSO2= 0.1 to 1 atm, the proportion of arsenic and bismuth in gas is predomi22t for the arsenic and bismuth distributions in both smelting and converting stages. The degree of vapour saturation has serious effect on the distribution, and sufficient contact between gas and matte phases is desirable for transferring arsenic and bismuth into gas phase.The elimination of antimony by means of vaporization is not significant. In reduction smelting at po2 = 10-11 atm, the proportions of arsenic and antimony in the gas phase are quite small, but the proportion of bismuth does not change significantly.

Jan 1, 1983

By Jian Li, S. Penttila, W. Zheng

"Materials selection for Gen IV supercritical water reactor in-core components faces major challenges due to severe operating condition. Beside high-temperature mechanical properties, SCC and general corrosion resistance of commercially available materials are also major focuses in recent research. Recent reports suggest that certain types of surface modifications are beneficial to SCW corrosion resistance. In this study, the effects of surface modifications are investigated, and possible mechanisms for improved corrosion performance are discussed.IntroductionThe current Canadian pressure-tube supercritical water reactor (SCW) design specifies a core outlet temperature of 625°C under 25 MPa of pressure, with peak cladding temperature as high as 850°C. Challenges in materials selection include high-temperature mechanical properties, corrosion resistance, SCC resistance and radiation damage. Most of the SCW corrosion test results available are below 730°C. Early work by Allen [1] summarized the corrosion resistance of alloy groups including Ni-based super alloys, stainless and ferritic/matensitic (F/M) steels that can potentially be used for SCW reactors. F/M steels can only be used at low temperature sites (e.g. down stream piping). At 500°C and 25 MPa, F/M steels develop a thick but mechanically stable oxide layer. However, the long term stability of the surface oxide layer is largely unknown. Ni-based alloys appear to form very thin surface oxide, however pitting was observed in the vicinity of some intermetallic precipitates [2-5], and dissolution of major alloying components could pose significant problems for down stream piping [6]. In addition, concerns of Helium formation due to Ni transmutation prevented this alloy group to be used as fuel cladding. The corrosion resistant austenitic stainless steels (e.g. 316L) are found to be susceptible to localized corrosion such as pitting, intergranular attack and stress corrosion cracking (SCC) [7]."

Jan 1, 2012

By Chenhui Liu, Ka-ma Huang, Hong-ying Xia, Bingguo Liu, Hua Chen, Jinhui Peng, Libo Zhang

"The rising popularity of microwave heating in mineral processing has fuelled the need for knowledge concerning dielectric properties of minerals. Dielectric property and microwave absorption property of anthracite were measured over a temperature range of 20-100°C at 2.45GHz by using an open-ended coaxial sensor measurement system. The results show that the dielectric constant, loss factor and loss tangent increase with temperature rising at 2.45GHz. Microwave absorption properties of anthracite are highly dependent on temperature and frequency. At frequency of 2.45GHz frequency used in microwave metallurgy, anthracite is suitable for reducing agent to achieve fast elevation of temperature then returning to original state. The research will be helpful in explaining the thermal running of microwave dielectric heating the anthracite.IntroductionThe application of microwave heating in minerals processing and treatment has recently attracted great interest from the metallurgical industry. Compared with conventional heating methods, the advantages of microwave heating include rapid and selective heating, uniform distribution, high efficiency, fast on and off switching as well as flexible and modular design[l-3]. As a result of these advantages, microwave heating has been applied in a variety of mineral processing and extractive metallurgy, such as microwave-assisted ore grinding, microwave heating for carbothermic reduction and acid leaching of ilmenite ore, microwave drying, microwave-assisted roasting and smelting of sulfide concentrate, microwave-assisted spent carbon regeneration and microwave-assisted waste management [ 4-6]. Though the application of microwave heating in the metallurgical industry is promising, further studies on the interaction between microwave radiation and minerals and its effects are highly desired to develop innovative techniques for minerals processing and ore treatment using microwave heating [7]."

Jan 1, 2013

By Jing Zhan, Chuanfu Zhang, Yonglin Yao

"The Ni/Co arbitrary ratios of fibrous precursor were investigated during coordinated coprecipitation by changing the precipitating medium. The results show that the original molar ratio ofNi2+ to Co2+ in reaction solution can be maintained in the coprecipitate at pH'.'05.0 and the coprecipitate is single phase solid solution using water and water-X precipitating medium. But the original Ni/Co ratios are no longer kept and composition of the coprecipitate is not uniform at pH>5.0 in water precipitation medium. In order to obtain the precursors with the required morphology and accuracy Ni/Co ratios, the optimum conditions of fibrous precursors were chosen as follows: ammonia used as complex agent and pH adjustor, water-X solvent as precipiting medium, oxalate as coprecipitated agent, 8.0-8.4 for pH value, 50-70°C of reaction temperature, 0.5-0.8 mol/L of initial nickel and cobalt salt concentrations and excesses of oxalic acid of 10% - 20%.IntroductionNi-Co alloy as an important transition metal alloy with high mechanical strength, good anti-deformation, corrosion resistance, thermal conductivity, thermal stability, electrical conductivity, electrical contact, and special magnetic properties indicates that it can be used as high-temperature catalyst, special magnetic material, high-temperature electrochemical devices, and so on [1-6]. An ideal composite powder should have an appropriate stoichiometric ratio, good uniformity of chemical composition, appropriate phase, low impurity content and small particle size [7]. Similarly, the composition of nickel-cobalt alloy powder has an important impact on its crystal structure, properties and applications. Guo[8] found that magnetisms of CoxNi1-x such as magnetic anisotropy, curie temperature, and the shifts of the spin steering are very sensitive to the composition of alloy powder."

Jan 1, 2013

By Guiming Yang, Xiaoxian Huang, Zhiyun Ji, Min Gan, Lishun Yuan, Xiaohui Fan, Zhiyuan Yu

"The roasting characteristics of hematite pellets containing MgO were studied where magnesia powder, serpentine and magnesite were used as magnesium-additives respectively. The mechanical strength of both preheated and roasted pellets decreased when MgO content increased, which implied the addition of MgO had an adverse effect on pellet consolidation. By adding flux containing CaO, the mechanical strength of both preheated and roasted pellets were improved. The addition of calcium flux facilitated the formation of calcium ferrite and provided a certain amount of liquid phase, resulting in faster diffusion ofMg2+ and Fe3+. The result showed that diffusing speed of Mg2+ was enhanced by 1.48 times, and rate constant of Fe203 crystalline growth was enhanced by 62% when basicity was around 0.4. Improvement of mineralization degree and recrystallization of Fe203 assisted in consolidation of hematite pellets containing MgO.IntroductionOxidized pellets are ideal iron-bearing burdens in blast furnace. At present, magnetite is the main raw material for oxidized pellet production in China. However, as the rapid development of iron and steel industry, resources of magnetite have been depleted and cannot satisfy the requirement of pellet production. Using hematite concentrates to produce oxidized pellets has become a trend [1, 2]. Many pellet enterprises abroad nowadays have adopted high proportions of hematite concentrates when producing oxidized pellets, e.g. the percentage is 100% in a lot of Brazilian factories [3, 4]. But high proportion of hematite concentrates will lead to low mechanical strength and high reduction swelling index of pellets. Some studies show that Mg-bearing pellets have excellent metallurgical properties, and the reduction swelling phenomenon can be solved by adding fluxes containing MgO [5, 7]. However, there are problems such as low pellet strength and bad roasting characteristics for MgO-bearing pellets, which remains an obstacle in pellet industry. Hence, it's vital to undertake the study on strengthening measures for indurations of Mg-bearing hematite pellets."

Jan 1, 2013

By M. Vijayalakshmi, S. Saroja, C. Sudha, T. N. Prasanthi

"Ti-5Ta-2Nb alloy and 304L austenitic stainless steel were joined by explosive cladding process. Investigations on 'as received' explosive clad revealed high hardness very near the interface due to martensitic transformation of 304L steel base plate. To improve ductility, explosive clads were heat treated in the temperature range of 823 to 1073 K for 1 to 20 h. Consequent change in the microstructure and microchemistry of the clad interface was studied. No change in the interface microstructure was observed for heat treatment at 823 K. Increase in temperature lead to the formation of various reaction zones at the interface, their number and width increase with temperature and time of thermal exposure. Growth kinetics of the reaction zones was monitored and activation energy required for formation was calculated. From elemental redistribution profiles, effective inter-diffusivities of alloying elements were calculated as a function of concentration and activation energy required for inter-diffusion was evaluated.IntroductionFor engineering components exposed to highly oxidizing and corrosive environments, a titanium based alloy i.e Ti-5Ta-2Nb (Ti-Ta-Nb) is often chosen as a structural material [1,2]. For economic consideration, vessels and piping exposed to non-oxidizing conditions are fabricated from 304L austenitic stainless steel (304L SS). Hence, dissimilar joint of Ti-5Ta-2Nb alloy and austenitic stainless steel becomes unavoidable. Fusion welding processes are not suitable for joining Ti and Fe based alloys due to the propensity for the formation of intermetallic phases and subsequent reduction in the bond strength [3,4]. Hence, explosive cladding, a solid state welding technique, was used to achieve high integrity, corrosion resistant joints between the two alloys."

Jan 1, 2012

By D. J. Adams

Cyanide heap leaching is the predominant technology used in processing low-grade gold ores. During closure ora heap leach operation, residual cyanide must be removed from the process and waste solutions, as well as the heap. Biological cyanide oxidation is a proven, economical technology for destroying cyanide in process and waste waters and spent heaps; The use of biological cyanide degradation eliminates the need for toxic or corrosive chemical oxidizers and has- been implemented at full scale at treatment costs usually <$0.50/1,000 gal. The Applied Biosciences biological cyanide destruction (BCND?) process has been demonstrated to effectively treat cyanide, concentrations up to 350 mg/L. Treated process solutions and wastewaters also contained other contaminants such as arsenic, copper, iron, silver. selenium, mercury, nitrate and zinc, much of which was removed in the cyanide degradation process. Under optimal conditions, microorganisms can rapidly oxidize free cyanide in some process solutions from over 250 mg/L down to 0.1 mg/L in 4 to 5 hr. Cyanide is degraded to ammonia and carbon dioxide, with 50%ofthe cyanide carbon liberated as C02. In general, carbon tank based bioreactors degrade cyanide at significantly higher rates than process or wastewater pond configured treatments, which usually degrade cyanide-more rapidly than in heap treatments. Investigation of cell-free enzyme preparations as an alternative to live microbial cyanide degradation shows promise. Advantages of enzymes over live microbes for cyanide degradation include: (I) the ability to tolerate and degrade higher cyanide concentrations (> I ;000 mg/L), (2) nutrients to support live microbial cells are not required, (3) the effects of other toxic contaminants, such as metals, found in mining waters-are eliminated and (4) the potential for greatly increased kinetics.

Jan 1, 1998

By Wei Gao, Qing-cai Liu, Cun-fang Lu, Huimin Zheng, Jian Yang, Chun-ling Yao

"Mercury in flue gas of coal-fired plants was concerned as another serious pollution when sulfur dioxide pollution was controlled now. The adsorbent made from fly ash by thermal precipitation sulfur to remove mercury in fuel gas from coal combustion plant, SEM, BET, TGA and other measurement methods were used to characterize the effect on surface morphology, sulfur distribution and specific surface. High temperature deposition furnace was applied to increase sulfur content in fly ash based adsorbents produced in lab. The study found that sulfur attached to the adsorbent surface, mesopore and microporous structure, increasing its sulfur content of adsorbent. Sulfur was filled in interspace as small molecule S2, S5, increased their surface area and enhanced their adsorption capacity. The specific surface area increased by thermal precipitation sulfur, and specific surface area which increased with increasing temperature.1. IntroductionThe mercury emission caused by human activity has accounted for 10%-30% of total mercury emission all over the world[11, and the emission from coal-fired power plant have a huge proportion of these emission caused by human activity. Active carbon microstructure and surface morphology play an important role in its adsorption capability, which offers the potential for controlling environmental pollutant, such as sewage, fuel gas, atmosphere and et al [2,31, because it is a material with high specific surface area that long been considered as an excellent adsorbent. At present, include activated carbon, fly ash, calcium-based sorbents and other novel adsorbents. The adsorption capacity and production cost were very important in the process of mercury removal by adsorbents, so the mercury removal has focus on developing adsorbents of highly-efficient. In particular, the waste of metallurgical from coal combustion and the others have a significant advantage about the cost, and they have the highly-efficient in mercury removal after modified to enhance their adsorption capacity, such as fly ash of coal-fired. Apart from specific surface area, element content, pore structure, and surface morphology of activated carbon have great effect on its adsorption ability. Compared to adsorbents without modification, active carbon impregnated with other elements, such as chlorine, sulfur, bromine and et al. had more excellent characteristics to remove specific pollutants."

Jan 1, 2011

By Jin Yu, Fang-Qiu Zu, Yun Xi, Li-Na Mao

"According to the behaviors of resistivity-temperature of Cu-Sb70 melt, which suggests a partly reversible temperature-induced liquid structure transitions (LST) could occur in this alloy, in this paper, we investigated the dependence of solidification on the liquid state. Both resistivity and temperature were measured to track solidification process. The results show that the nucleating undercooling of the melt which experienced the LST increased and the solidified time decreased. Meanwhile, the solidified microstructures refined evidently, with the microscopic pattern of primary phase changes from disordered pillarlike dendrites into homotaxic ones. Moreover, it is verified that the microstructures would be different if the reversible part of the LST was restrained. The new phenomena and results reflected in this paper suggest that grasping the rules of melt structure change with temperature before material processing will give help for controlling the solidification more effectively and finally resulting in more ideal microstructures.IntroductionThe structure and quality of liquid alloys have a direct and important influence on the structure, performance and quality of the solidified ones. In recent years with in-depth study of liquid structure, researchers have found that some liquid structure transitions (LST) could occur on dependence of the temperature or pressure [1-5]. And the article [6] reported that a pressure-induced reversible LST was found in liquid triphenyl phosphite, which further confirmed the authenticity of the existence of the LST. Furthermore, in our earlier studies of Sn-based melts using resistivity method, some abnormal structure changes induced by temperature have been found at hundreds of degrees above liqiudus, and these LSTs are partly reversible[7]. This phenomenon has been discussed and it is suggested that the reversible LST in Sn-based melts are related to the short-range ordering (SRO) structures of Sn, which are tetrahedron structure with covalent bonding. However, does this reversible LST exist in other melts too?"

Jan 1, 2012

By Ji-He Wei

The ESR of Cu-Cr-Zr alloy has been experimentally investigated. The remelting experiments have been carried out with different slag fluxes in the Cal, + Nal, CaF2 + ZrO2 and CaF2 + NaF + ZrO2 systems on an ESR furnace of 25kg capacity; using a water-cooled copper mould of 96.5 mm diameter, with the forged square bar electrodes of 50x50 mm2. The slag amount was taken to be 1.5 kg. The remelting current and voltage used were 1600-1800A and !5-25K, respectively. The influence of the slag composition on the stability of the remelting process and the losses of alloying elements (2r and Cr) has been considered and examined. The technologies of hot working and heat treatment of the ES ingot have been described and discussed. Some physical properties of the slag in a CuF2 + NaF + ZrO2 system and the remelted Cu-Cr-Zr alloy have been determined. The results indicated that with the slag flux of CaF2 + NaF + l0 mass % ZrO2 and the other operation parameters employed, a high quality ingot of Cu-Cr-Zr alloy may be obtained at the considerably high yields of Zr and Cr by means of ESR. For the remelted Cu-Cr-Zr alloy with a specified composition of 0.5 mass % Cr and 0.1 mass % Zr, the appropriate electrical conductivity, hardness and softening temperature are as high as 45-46S/m, HRB 82-84 and 550°C. respectively. The properties of the Cu-Cr-Zr alloy products are in accordance with and superior to the requirements and specifications of ISO5l82-l99l(E).

Jan 1, 2000

By Singareddy R. Reddy, Ramana G. Reddy

"The Margules equation is used for interpreting excess Gibbs energy of several ternary systems. An expression for the activity coefficient of a dilute solute, 2(oxygen), in a binary solvent 1-3 is derived. It is used to calculate the logarithmic activity coefficient of oxygen in Pb-O-Gu, Pb-O-Bi, AgO- Sn, Pb-O-Sn and Ag-O-Pb metallic systems. Self interaction parameter of the solute is derived from the partial Gibbs energy of solute using constant compositional path. The derived equation is used successfully to deduce the self interaction parameter of oxygen in Pb-O-Gu and Pb-O-Bi metallic systems. The predicted thermodynamic parameter data i.e activity coefficient and self-interaction parameters are in an excellent agreement with the experimental data and also our predictions are far more accurate than the predictions made by other models.1 IntroductionThe nature of solute interactions such as oxygen, nitrogen and sulfur with the metallic solutions are important for a number of chemical and metallurgical processes. Several theories [1-23] have been developed to evaluate fundamental thermodynamic properties of solutes constituting two elements. The activity of solutes has been calculated using statisticalor quasi- chemical approach.Wagner's [4] Ideal Solvent Model is based on one energy parameter to describe the compositional dependencies of the activity coefficient of nonmetallic solutes such as oxygen in binary metallic solutions. This model depends on a constant energy of interaction for the exchange of atoms from the coordination shell of an oxygen atom to the shell of an interstitial site and cannot account for properties of strongly interacting systems [4]. Therefore, several attempts have been made to improve the Wagner's model for the strongly interacting systems. [10-16]."

Jan 1, 1996

By E. Bélisle, Christopher W. Bale, S. Petersen, C. Robelin, K. Hack, J. Melançon, G. Eriksson, A. D. Pelton, P. Chartrand, S. A. Decterov, I. H. Jung, A. Gheribi

The FactSage® package consists of a series of information, database and calculation modules that enable one to access pure substances and solution databases and perform thermochemical equilibrium calculations. FactSage was originally founded by process pyrometallurgists and has since expanded its applications to include hydrometallurgy, electrometallurgy, corrosion, glass technology, combustion, ceramics, geology, environmental studies, etc. With the various modules one can perform a wide variety of thermochemical calculations and generate tables and graphs of complex chemical equilibria and phase diagrams for multicomponent systems. This paper presents examples of recent and current developments in FactSage in areas of particular interest to Dr. David Robertson. These include both ferrous and non-ferrous processing, as well as solidification and refining simulation. The paper also includes reference to the Internet Fact-Web education package.

Jan 1, 2014

By G. Kyle Green

Zirconium chlorinator residues contain an array of rare earths, scandium, unreacted coke, and radioactive thorium and radium. Because of the radioactivity, the residues must be disposed in special waste containment facilities. As these sites become more congested, and with stricter environmental regulations, disposal of large volumes of wastes may become more difficult. To reduce the mass of disposed material, the U.S. Bureau of Mines (USBM) developed technology to recover rare earths, thorium and radium, and unreacted coke from these residues. This technology employs an HCl leach to solubilize over 99% of the scandium and thorium, and over 90% of the rare earths. The leach liquor is processed through several solvent extraction stages to selectively recover scandium, thorium, and rare earths. The leach residue is further leached with an organic acid to solubilize radium, thus allowing unreacted coke to be recycled to the chlorinator. The thorium and radium waste products, which comprise only 2.1% of the original residue mass, can then be sent to the radioactive waste facility.

Jan 1, 1995