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Electrocrystallization studies were conducted in a concentrated acid-copper electrolyte to determine the influence of chloride ions and glue on copper nucleation and on the structure of thin copper layers. Electrochemical experiments allied to SEM and XRD examination were performed to characterize the mechanism of nucleation in the presence of additives at 65°C. Results indicated that most of the copper nucleation from a 83 g dm-3 Cu2+ solution, with 140 g dm-3 of H2SO4 is achieved in a matter of milliseconds, Although the presence of chloride and glue, at the concentration levels tested, does not seem to substantially modify the nucleation mechanism, the morphology, nuclei density and the copper film structure and orientation are changed by the presence of additives and by electrolyte stirring.

Jan 1, 1999

By Takahiko Okura

Sulphur, with its multiple oxidation states, play critical roles in many processes, ranging from regulating enzymes in plants, to acidifying aquatic systems, and to affecting the global climate. Most of non-ferrous smelters have been contributing to reduce atmospheric emissions of sulfur dioxide to acceptable levels, converting it to sulphuric acid and/or gypsum. However, some amount of SO2 gas is still emitted from isolated smelters. Furthermore, sulphuric acid is competing with involuntary elemental sulphur in the market. This situation puts the non-ferrous metallurgical industries to develop a new sulphur fixation process. This paper briefly describes the new technologies for fixation, followed by the novel proposal to convert SO2 gas to elemental sulphur using organic materials. Finally, the feasibility will be presented technologically and economically.

Jan 1, 2006

By San-chuan Tang, Wen Chen, Shun-ming Ning, Kan-ping Yu, Qiang Zhao, Xue-yong Xing

"A new type of desilication agent (PA-2) was selected by experiment based on the analysis of the characters of silica gel, and the influence of desilication type, desilication dosage, pH value, temperature and aging time on the desilicating effect was studied. The test results showed that on the conditions that pH was 2.0, temperature was 20""C, aging time was12 hours and the dosage of desilication agent was 0.23%, the desilication rate was higher than 93% in solution.IntroductionVanadium is an important strategic resources, which applies to steel industry and petrochemical industry. The main materials for vanadium product are steelmaking vanadium slag, stone coal and containing vanadium waste catalyst, etc. And stone coal is a low-grade carbonaceous silicified vanadium resource, which is unique material for vanadium extraction in China. Meanwhile, our stone coal reserves is No.l throughout the world.The silica acid solution containing vanadium is produced by acid leaching of raw stone coal or its roasted ore. The silica content of this solution is mostly high, besides, when pH is higher than 2 , the solution is unstable. Furthermore, it is very easy to generate gel substance with the increasing of pH value and standing time. 'Ibis silica gel is composed of colloidal particles with the size in 0.001 - 0.1 um. As a result, it is very hard even impossible for the following operation of solution."

Jan 1, 2013

By Toshiyuki Hashida, Victor M. Lopez-Hirata

"Small-punch tests and determination of fracture toughness JIC were conducted at 4 and 77 K on new cryogenic JN1, JJ1 and JK2 austenitic stainless steels, after isothermal aging. Equivalent fracture strain ?qf determined by measuring the reduction of thickness in the small-punch test specimen. A linear dependence of JIC on ?qf was found in these new materials. Regression analysis of experimental data produced the following linear relation JIC = 1304.1 ?qf + 8.09 [kJm-2]. An analysis of present work relation was pursued on the basis of material properties and evaluation method of he. Results showed that the slope value has a strong dependence on material yield strength and JIC evaluation method. This linear relation is useful for the evaluation of fracture toughness JIC, measuring the equivalent fracture strain ?qf by means of small-punch test. Thus it can be useful for assessing the degradation of fracture toughness in small areas such as, the heat-affected zone in welded components.IntroductionCryogenic structural materials for superconducting magnets of fusion nuclear reactor are required to possess a good combination of strength and toughness. The mechanical properties are required beyond the capability of conventional austenitic stainless steels [1]. New cryogenic JN1, JJ1 and JK2 austenitic stainless steels were developed by the Japan Atomic Energy Research Institute (JAERI) [1]. The structure of superconducting magnets is constructed by welding of 200 = thick plates of these steels, which are solution treated at high temperatures and then water-quenched to avoid intergranular precipitation. However, the welding process involves heating and cooling [2], which cause microstructural changes in both base metal and weld. In this heterogeneous microstructure, it is important to estimate the fracture toughness of these materials at cryogenic temperatures. Therefore, it is necessary to evaluate the effect of aging process on the fracture toughness behavior of these new steels. To determine the cryogenic fracture toughness, the elastic-plastic JIC value has been co=only used [2]; however, the specimen size is much larger than heat-affected zones in welded components. Small-punch (SP) testing method, employing miniature specimens, has permitted to evaluate the fracture toughness behavior at different temperatures in different nuclear reactor materials [3,4]. Mao et al. [5,6] and Misawa et al. [7] found a linear relation between JIC value and equivalent fracture strain ?qf, determined by SP method in non-ferrous alloys and ferritic steels at room temperature and austenitic stainless steels at 4 and 77 K, respectively. So that, this kind of correlation would be very useful to assess the fracture toughness JICe values by means of SP test in small zones of welded components."

Jan 1, 2012

By Adam Powell, David Dussault

"Electric Field-Enhanced Smelting and Refining is a process for driving the reaction between carbon in hot metal and iron oxide in slag, for example, in a steelmaking reactor. This process involves inserting electrodes into the slag and metal phases, such that the overall reaction FeO + C -> Fe + CO is separated into two half-cell reactions: Fe2+ + 2e· -> Fe at the cathode in the slag, and C + O 2 • -> CO + 2e· at the anodic slag-metal interface. Without the electrodes, the reaction is very slow, but with electrodes, the additional surface area available to the ferrous ions for reduction accelerates the reaction even without any applied bias. When a bias is applied to the electrodes, the electric field across the slag further accelerates the overall reaction.With or without applied bias, the process is first-order in the ferrous ion concentration, and limited by ferrous ion transport to the cathode. To complicate matters, as the liquid iron is reduced at the cathode, the Mullins-Sekerka instability leads to formation of dendrite-like liquid iron fingers which grow into the slag. Because of this, the design of the cathode can have a significant effect on the overall process kinetics, and understanding of the dynamics of these fingers and of their effect on mass transfer is necessary for the intelligent design of the overall process and the cathode in particular.Toward this end, a detailed mesoscopic two-phase slag-metal model is presented here which describes multi component diffusion in the slag and fluid flow in both phases in the vicinity of the cathode. Diffusion in the slag is driven by chemical and electrical potentials. The phase boundary is modeled as a diffuse interface using a phase field approach. Because this electrochemical reaction occurs at high-temperature, the kinetics of charge transfer and adsorption through the double layer are fast relative to transport, permitting the use of simple linear reaction kinetics. This also eliminates the need to discretize the double layer, with the result that charge neutrality may be assumed everywhere in the domain. Introducing electric field dependence of the gradient potential and well height coefficients in the free energy function allows the model to capture electrocapillarity at the interface."

Jan 1, 2001

By Teruhisa HORITA

The durability of SOFCs is one of the critical issues to realize the SOFC systems. In order to improve the durability, a precise degradation mechanism should be clarified at the different functional ceramic interfaces in SOFC cells and stacks. This paper reviews the improvement of SOFC durability by the mass transport analysis especially at cathode/interlayer/electrolyte interfaces. We have made a precise analysis on the reaction of cathode with impurities. Especially at the (La,Sr)(Co,Fe)O3/CeO2/ZrO2 interfaces, a significant amount of SrCrO4 and SrSO4 were observed at the (La,Sr)(Co,Fe)O3 surface as well as inside the (La,Sr)(Co,Fe)O3 cathode, which suggested some process occurred for both poisoning. Possible degradation mechanisms were proposed based on the observation data.

Jan 1, 2016

By Jae-Woo Ahn

Waste acids containing phosphoric, acetic, nitric and hydrofluoric acid were produced during the etching process of liquid crystal display and semiconductor manufacture. In recent years, the attention on the treatment of industrial waste acids has been increased considerably according to the reinforcement of the environmental regulations as well as the implementation of the economic considerations about the waste acids. Fundamental studies on the separation and regeneration of the mixed waste acids were conducted using Cyanex 923, Tri-octyle phosphate and 2-Ethylhexyl alcohol as an extractant by solvent extraction. It is considered that the extraction of liquid crystal display waste acids with Cyanex 923 and Tri-octyle phosphate, semiconductor waste acids with 2-Ethylhexylalcohol is applicable for the separation and recovery of acid. Finally, the acceptable recycling process from the multi-component waste etching acids was proposed.

Jan 1, 2006

By Peng Peng, Ouo Cheng, Guodong Lai, Lijuan Chu, Zebiao Zhang

"The pressure acid leaching residue of zinc concentrate contains a large quantity of sulfur. The present study attempts to leach sulfur using a mixture of ammonium sulfide and water solution at 25°C. Effects of three leaching variables: ammonium sulfide concentration, leaching time, liquid/solid ratio on the sulfur leaching rate were investigated. The process conditions were optimized using response surface methodology based on the central composite design. From the analysis of variance (ANOVA), the significant factors on response were identified. The optimum conditions for leaching elemental sulfur from pressure acid leaching residue of zinc concentrate were obtained using an ammonium sulfide concentration of 2.5 mol/L, leaching liquid-solid ratio of 6.5:1 and leaching time of 7 min. Under the optimum experimental conditions, a maximum of 98.50% of total sulfur was extracted. The experimental results obtained agreed satisfactorily with the model predictions, with a correlation coefficient (R2) of 0.99.IntroductionSulfur is widely used in agriculture, medicine, rubber, building materials, gunpowder, wine and sugar, and other fields [1]. Currently the world sulfur production is 40Mt, out of which more than 90% is recovered from industrial processes, and 10% is natural [2], This highlights the importance of sulfur recovery. As the pressure leaching technologies [3] continue to mature and are increasingly applied to refining, a large quantity of high-sulfur residue is produced [4-5]. It is desirable to recover sulfur from this residue, so that it is economically advantageous, and reduces environmental pollution [6]."

Jan 1, 2012

By T. T. Chen

The manganese oxide scales, consisting mainly of MnO2, characteristically occur in banded colloform structures which adhere to porous layers of PbSO4 and PbO2 that oxidized from the rolled Pb-0.7% Ag anodes. Hydrous Mn oxides, Mn3O4 and amorphous Mn oxides are believed to be also present. Tiny particles of gypsum, PbSO4, SrSO4 and AgCl are entrapped in the colloform masses. The gypsum originated from the Zn electrolyte; strontium carbonate was added to the ZnSO4 solution to control Pb, and silver originated from the anodes. Some of the colloform bands contain minor amounts of Pb, implying a limited degree of dissolution of the Pb during electrolysis. Other colloform bands incorporate trace amounts of Zn. Colloform structures permeated with silica gel are presumably caused by the high silica content of the electrolyte.

Jan 1, 2009

By Wantae Kim

In order to establish the optimized recovery process for heavy minerals from Korean beach sand, we investigated the several physical separation methods such as gravity and magnetic separation followed by mineralogical characterization. There was clear relationship between the particle size and heavy mineral content that heavy minerals were mostly concentrated in the particles below 100mesh. Gravity separation using the spiral and shaking table separators made it possible to concentrate heavy minerals by rejecting the light and coarse particles consist mainly of quartz and other non-valuable minerals. The high-intensity magnetic roll separator and subsequent induced magnetic separator were applied to fractionate magnetic particles according to their magnetic susceptibility. The content of TiO2 of high susceptible ilmenite-rich fraction was 43.98wt.% while those of ZrO2 of non-magnetic and magnetic residue were 6.78wt.% and 3.11wt.%, respectively.

Jan 1, 2006

By Kejun Liu

Platinum and palladium are usually dissolved together and followed by separation. In this study, the selective leaching of platinum and palladium from a secondary resource, such as dental waste, by using chloride solution (hypochlorite and chlorate) has been developed. Results indicate that about 100% of palladium could be initially extracted by the combination of 0.3 mol/L sodium hypochlorite (NaClO) and 0.068 mol/L sodium chloride (NaCl) at pH 1.2 and 298K in 1.5 hours, or the combination of 0.005 mol/L sodium chlorate (NaClO3) and 6 mol/L hydrochloric acid (HCl) at 298K in 0.5 hour. About 100% of platinum could be extracted from the residue by the combination of 0.47 mol/L sodium chlorate (NaClO3) and 12 mol/L hydrochloric acid (HCl) at 298K in 2 hours.

Jan 1, 2003

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

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

Jan 1, 2008

By Gerald K. Vellente

Producers of strip coated products are being approached by users to supply higher quality products and adhere to tighter specifications. Suppliers, in an attempt to assist the producers, must consider new technologies for equipment. In the past several years, the induction melting and heating industry has made great strides in developing new and innovative equipment, while improving existing technology. In the past several years, the induction melting and heating industry has made great strides in developing new and innovative equipment, while improving existing technology. In the past several years, the induction melting and heating industry has made great strides in developing new and innovative equipment, while improving existing technology. This paper will review recent developments to include improved refractory systems for ceramic pots, new channel-type inductors which are more efficient, new power control systems for existing channel-type pots, and innovative use of multi-purpose lines. Additionally, new heating applications such as galvannealing, edge heating, and post heating will be reviewed. Advanced math models for controlling heat will be discussed. Producers can easily meet the demands of their customers because of the flexibility provided by the equipment reviewed.

Jan 1, 1992

By V. A. Luganov

During the treatment of raw materials containing arsenic and antimony, problems in the distribution of these elements in the process products occur. In a number of cases in processing of copper-bearing materials, it is possible (or necessary) to obtain speiss. The purpose of the present research is to study the theoretical aspects and analyze the technological possibilities of producing copper-bearing speiss and the subsequent electrometallurgical processing with copper extraction as well as arsenic and antimony utilization. Copper arsenide (Cu3As) and copper antimonide (Cu3Sb) are the main components of the speiss. A thermodynamic analysis of the electrochemical oxidation of Cu3As and Cu3Sb, carried out using Pourbaix diagrams, showed that in a pH range from 0 to 2, oxidation potential 0.45-0.55V, ions of copper and arsenic and antimony trioxide are in the equilibrium. The kinetic study has shown, that with an increase in the polarization potential, the dissolution process changes from chemical to diffbsion control. An increase in temperature stabilizes the electrolysis process due to dissolution of arsenic trioxide forming on the anode. Electrolysis of speiss using a cathode diaphragm with the solution pH = 1-2, current density 150-200 A/m2 and temperature 60-70°C makes it possible to obtain cathode copper with a current efficiency of 95-96% and to remove the arsenic from the process during the electrolyte cleaning process. The arsenic content in the cathode copper did not surpass 0.002%. As the result of the research, a technological flowsheet for copper-lead speiss processing was developed. At the present time this technology is undergoing pilot testing.

Jan 1, 1999

By Mei Song, Qingyu Deng, Xuewei Lv, Lu Liu, Chenguang Bai, Meilong Hu

"The carbochlorination of several silica materials was carried out in the temperature range from 900 °C to 1200 °C. In this study, silica oxides and gaseous chlorine with carbon as reductant were used. The optimal carbon silica mole ratio in different temperature was calculated by Factsage software and the results showed that the optimal values are 1.2, 1.4, 1.6, 1.8 at 900 °C, 1000 °C, 1100 °C, 1200 °C, respectively. According to the experiments, the chlorination ratios of several silica materials were increased with temperature increasing. In the same temperature, the chlorination ratio of diatomite is the maximum and the chlorination ratio reaches 79%% when C/SiO2 reaches 3 at 1100 °C.1, IntroductionPolycrystalline silicon is the main material to manufacture the silicon polished section, solar battery[1] and high purity silicon wafers[2], also which is the most basic function material of semi-conductor industry, electronic information industry and solar photovoltaic battery industry[3]. The conventional manufacturing process of polycrystalline silicon would be divided into three parts: the improved Siemens method, which was introduced and became the main process to produce the polysilicon products in China. Silane method and fluidized bed method. Silicon tetrachloride and chlorosilans have been employed as by-products in several fields like electronic, telecounications and metallurgy[4-6]• At present, the main applications of silicon tetrachloride include production of trichlorosilane by catalytic hydrogenation, synthesis of fumed silica and ethyl orthosilicate, production of optical fiber grade silicon tetrachloride.The conventional routes for the silicon tetrachloride production have been reported, including the direct chlorination and the chlorination process of ferrosilicon, abandon catalyst and silica[7]."

Jan 1, 2013

By Shan He, Qiang Wang, Xuling Chen, Min Gan, Lishun Yuan, Xiaohui Fan

"The sintering properties of vanadium-titanium magnetite concentrate(VTC) was studied in this paper. Through the optimizing the sintering process of VTC, the suitable granulation moisture and coke proportion were determined. The sintering velocity decreased from 23.05 mm/min to 18.22 mm/min. With the increase of VTC proportion from 0 to 46%, the specific productivity and tumbler index were respectively decreased from 1.55 t/(m2·h) to 1.21 t/(m2·h), and 62.93% to 57.73%. The temperature of liquid phase formations of mixtures increased, the amount of liquid lowered, and the content and sharp of sintering mineral gradually changed with the increase of VTC ,these lead that sinter quality became worse.IntroductionIn recent years, the steel industry of China is developing rapidly. And the steel production was 627 million tons in 2010. At present, the resources of vanadium-titanium magnetite concentrate(VTC) was about 14.4% of the total national iron reserves of China[1]. VTC has been used as sintering material by Magang, Chenggang and Pangang. The amount of VTC in Pangang is maximum. However, there exist many problems in VTC sintering, which involve in high specific productivity, bad sintering tumbler strength and high energy consumption[2~5]. That’s why the proportion of VTC is limited in sintering.The high quality of iron ore resources is worse in China. Therefore, it’s necessary to study the properties of VTC sintering, and to find out the reason how the VTC ratio affect the sinter performance. Purpose and significance of the research is to get high-quality sinter with the proportion of VTC greatly raised."

Jan 1, 2012

By Eiki Ono, Atsushi Yamatodani, Shigeru Sunagawa, Yasushi Takasaki, Atsushi Shibayama, Yasunori Higuchi

"During metallurgical processing of non-ferrous metals, smelting residue (inc. smelter slag, flue gas and so on) is inevitably generated as secondary product.In this research, some experimental feasibilities were investigated to recover/remove Cu and As from the residue. Primarily, the removal of As and volatilized materials from the residue was examined by pyrometallurgical treatment (dry-process). In the second stage after treating the residue with a dry-process, leaching and solvent extraction as hydrometallurgical treatments (wet-process) were also investigated by using H2SO4 solution as a two stage leaching treatment, to dissolve various metals from the leach residue. Then, solvent extraction was examined by using LIX-84I as an extractant to recover and separate Cu from impurities from the final (2nd) leached solution. For the leaching stages, the removal of 90 % As and the leaching rate of 85 % Cu could be achieved by 0.25 mol/l and 1.0 mol/l H2SO4 solution, respectively. On the other hand, the extraction of over 90 % Cu and stripping was carried out by solvent extraction. 1. IntroductionIn metallurgical process for non-ferrous metals, smelting residue (inc. smelter slag, flue gas and so on) is inevitably generated as secondary product, i.e., flue dust, slug and so on. The smelting residue includes some useful metals and undesired toxic materials; Cu, Pb, Ca and As, etc.In Japan there is one undisclosed place stockpiled with 10,000 ton of smelting residue from abandoned smelters about 25 years ago. Therefore it is necessary to reduce the residual amount for space and environmental protection including water treatment by separating and removing toxic materials."

Jan 1, 2008

By A. V. Tarasov

In order to improve technical, economic and environmental performance of hydrometallurgical processing of intermediate products containing copper and nickel, the Gintsvetmet Institute and the IMET Institute of the Russian Academy of Sciences have conducted studies into the efficiency of the use of alternating current of industrial frequency on processes applied for hydrochemical leaching of various copper- and nickel-containing materials. It has been found that: 1.Imposition of alternating current over the process of leaching of softly reduced nickel oxide with recycled copper sulfate solutions resulted in an increase by 20 to 30% of the rate of the copper cementation process and reduced by 20% its activation energy. At the same time, the recoveries of nickel, cobalt and iron to the leach solution increased up to 82.2%, 78.5% and 57.1%, respectively, and that of copper to the cement precipitate up to 74%. Optimal process conditions have been identified with respect to the current density, electrode material, copper concentration in solutions and the process temperature. 2.In the process of hydroelectrochemical sulfuric acid leaching of nickel and copper sulfides, the grain size, the phase form of sulfides, the solution composition (H2SO4, Cl?, Cu2+, Fe3+)and the current amperage had an effect on the nickel recovery to the solution, which reached 90%, while the degree of copper transfer to solution did not exceed 20%. The process of hydroelectrochemical sulfuric acid leaching of nickel and copper sulfides with an addition of Cl? made it possible to selectively recover nickel into the leach solution along with concentrating copper in the leach residue. 3.When subjecting samples of commercial-grade magnetic fractions of converter matte to sulfuric acid leaching, the imposition of electric current, the concentrations of sulfuric acid and chloride ion in the solution and the duration of the reaction process had an effect on the process. The nickel recovery was 85% and that of cobalt and iron was 95% and the recoveries reached 97.5%, 98.3% and 99.8% as a result of repeated treatment of the primary residue under similar process conditions. Up to 75% of copper, 75% of sulfur and 99.0-99.5% of palladium was concentrated in the solid reach residues. The experimental data obtained indicates that the use of AC for hydroelectrochemical sulfuric acid leaching for separation of copper- and nickel-containing intermediate products has favorable prospects.

Jan 1, 2003

By Wang Haibei

China is the important country in terms of Ga, Ge reserves and products. These elements usually associate with lead and zinc ores such as in Fankou, Dachang and Lanping mines. Until now these metals could not be extracted from zinc residues effectively. The main reason is that it is difficult to separate zinc and iron. BGRIMM has carried out considerable research on this subject and some hydrometallurgical processes were developed. Zinc residues were pressure leached with a reducing agent such as zinc concentrates or SO2 at 110~130C. The final concentrate of H2SO4 was 30~50g/L. The metals such as Zn, Fe, Ga and Ge were dissolved into solution. In the leaching residue Pb and Ag could reach 20% and 2000g/t. The feed of solvent extraction was prepared from the leaching solution by pre-neutralization ? precipitation of Ga, Ge and acid dissolving. Then Ga and Ge were extracted by solvent extraction through P204 and G315 produced by BGRIMM. After stripping, metallic Ga was produced by electrowinning. GeO2 was produced by precipitation. The iron in raffinate was removed by the hematite process. The solution after removal of iron came back at the zinc neutral leaching stage. In 2003-2004, pilot tests were finished in BGRIMM in cooperation with Fankou Lead and Zinc Mine Ltd. And the extraction rate of Ga and Ge in the leaching stage was 94% and 83% respectively. The total recovery rate was 90% and 80%. It is estimated that the technology has a wide commercial use in the coming five years.

Jan 1, 2006

By Zheng Wei, Jian Cheni, Zhenliang Weng, Wei Liang, Hongbo Zhu, Jinhui Peng, Linqing Dai, Qianxu Ye

"By testing the dielectric constant and the dielectric loss factor of concentrated Dahongshan, mill scale, anthracite and light-burned dolomite in different frequency and temperature, and by studying the temperature-rising characteristics of the materials in the microwave field of 2.45GHz in frequency, the research in the paper shows that to reach at 1250°C under the same condition -2KW the microwave power and 30g the mass --the time concentrated Dahongshan takes is 330s, whereas the millscale is 855s and the anthracite is 820s. About the last one, the higher the temperature is, the stronger the absorptivity is. After the temperature has rose to 400°C, the anthracite's absorptivity increases dramatically. The result of the research would serve as the foundation of the further study on making direct reduced iron by microwave heating.1. IntroductionUnder the microwave fields, materials' dissipation of dielectric bodies would generate thermal effect. Therefore, the dielectric constant and the dielectric loss factor are closely related to materials' ability of absorbing microwave energy-the larger the dielectric constant and the dielectric loss factor are, the stronger the material's ability of absorbing microwave energy is, and the better the thermal effect would be[1-2]. In order to research how to make reduced iron from iron ore fines by microwave heating deeply and systematically, the test of raw materials' dielectric constants and dielectric loss factors are of the essence. What's more, because a mineral' conductivity is influenced by its components and crystal structure[3], it is necessary to study different materials' different temperature-rising characteristics; hence such studies would provide theoretical foundation of further research."

Jan 1, 2012