Search Documents

By Maria D. Salazar-Villalpando, Anthony Cugini, Bryan Reyes

"The electrochemical reduction of CO2 was performed in a laboratory-made, divided Htype cell. A copper electrode was used as the cathode. An Aldrich Nafion 117-type ion exchange membrane (0.18mm thickness) was used as the diaphragm. NaHCO3 and KHCO3 were studied as the catholytes. Hydrogen evolution from water reduction and products from CO2 electrochemical conversion were recorded. Higher CO2 reduction enhancement was observed by KHCO3 as compared to NaHCO3. The main conclusion of this work is that in fact CO2 can be electrochemically reduced with copper electrodes.1.-INTRODUCTIONThe direct electrochemical reduction of CO2 may allow for a simple process and, by avoiding high temperature reactors, would enable the process production rate to be quickly varied to follow the time of day availability of surplus electricity [1]. Temperature has a major effect on the electrochemical conversion of CO2 since its solubility increases when temperature decreases [2]. The electrical potential applied to the electrochemical reacting system will have an influence on the product distribution, as well. For example, a narrow potential range during cyclo-voltagraphic studies will determine the detection of a lower number of products. A recommended potential range to study the electrochemical reduction of CO2 is -2V to 2V. Moreover, the reaction rate on the electrode is governed by various processes, such as the kinetics of electron transfer, adsorption/desorption at the electrode surface, and diffusion of CO2 to the Cu electrode. The availability of active species, CO2 for electro-reduction, is extremely low at the vicinity of the electrode surface and it seriously interferes with the rate of mass transfer. In batch type electrolytic reactors, depletion of CO2 at the surface takes place first. CO2 from the bulk then has to diffuse to the electrode surface, resulting in mass transfer controlled kinetic phenomena. During the above process, several other competitive side reactions could suppress the primary reaction even though the cathode has good electro catalytic properties for reduction of carbon dioxide. When the dynamic supply of specific active species is ensured to electrode surface, the mass transfer effects are minimized to certain extent. Hence it is envisaged that a continuous flow reactor is more efficient for the electro-reduction of CO2 in CO2 saturated aqueous electrolytes. The primary reactions that occur at the copper electrode during the reduction of CO2 are listed below (with the standard potentials calculated using formation energies [1] :"

Jan 1, 2010

By M. J. Adam

As part of its research programs, the Bureau of Mines is investigating the partitioning of complex sulfide minerals to simpler sulfide phases by sulfidation reactions. Partitioning in this manner can afford opportunity to improve selective extraction of mineral constituents of value. This report describes research involving the sulfidation partitioning of the mineral pentlandite, which is an important source of Ni in primary production. For the laboratory studies, the pentlandite was synthesized in nominally equiatomic proportions of Ni and Fe. Elemental Ni, Fe, and S powders were blended, compacted, and sealed under reduced He pressure in vitreous silica tubes. The tubes were heated under controlled conditions at SOD? C for 24 h. The product was verified by X-ray diffraction and chemical analysis to consist essentially of (Ni,Fe)9S8. Small samples of the (Ni,Fe) S were encapsulated with sulfur in silica tubes at reduced He pressures and heated for 1 to 24 h at specific temperatures between 400? and 600? C, both below and above the boiling point of sulfur (_445° Cl. Reaction rate increased with temperature. Within this temperature range, partitioning to individual Ni and Fe disu1fides proceeded to essential completion according to the reaction

Jan 1, 1988

By Kosei Morita, Osamu Nakano, Katsuhiko Nagai, Kazuhiro Mori

"The Sumitomo Toyo Smelter and Refinery commenced its operation in 1971 with three Peirce- Smith (PS) converters. “2 hot – 1 blowing” operation was practiced, that is one of two available converters was blowing and the other was standby in a hot state while the third converter was under repair. After several improvements, the stack time ratio reached around 90%; and processing 5 batches a day became possible.As a result of the expansion program of the Toyo smelter and refinery that started in 2001, the converter operation pattern was shifted from “2 hot – 1 blowing” to “2 hot – 2 blowing” with the installation of second converter blowers and an additional ladle crane.In 2005 a, the fourth converter was installed and “3 hot – 2 blowing” operation began. Also, with improvements experienced in the anode furnaces and the anode-casting wheel operation, today, the number of cycles has been increased up to more than 8.5 a day.The treatment techniques of fugitive gas containing sulfur dioxide from converter furnaces have been gradually reinforced, and the fixation rate of treated sulfur is currently being maintained at more than 99.9%. This paper introduces the operations described above, and the improvements in environmental management techniques for the Toyo PS converter operation."

Jan 1, 2009

By Kouji Mimura, Tamas Kekesi, Yongfu Zhu, Masahito Uchikoshi, Minoru Isshiki

"The formation and anion exchange sorption of chloro complex ions can offer a great potential to be utilized for the separation and purification of metals in aqueous solutions. Available stability data were primarily used to estimate the predominance of chloro complex species, indicating the feasibility of such separations. Anion-exchange sorption functions, describing the equilibrium distribution of a number of important elements have been determined by the batch equilibrating method in the practical HC1 concentration range. Various oxidation states were stabilized by the addition of appropriate agents. Tendencies in oxidation, complex formation and anion exchange sorption were confirmed by spectrophotometric investigations. Based on the fundamental results, anion exchange processes have been developed for the purification of iron, cobalt, copper and zinc. The efficiency of separation was assessed and the procedure optimized by the analysis of experimental elution curves. Results have demonstrated that by properly controlling the oxidation states and HC1 concentrations, practically all the impurities can be eliminated. Computer programs have been developed to estimate complex formation and redox equilibria, to screen and correct analytical data, to determine distribution coefficients and to evaluate efficiencies of separation.IntroductionBase transition metals have long been used as the staple materials in various fields of industry. In general, there has been an increasing tendency in purity requirements but recent advances have created a rapidly increasing demand for ultra-high purity metals. To give a few examples, ultra high purity copper can be used as bonding wire and interconnection in integrated circuits, or as material for superconductor stabilizing, high-field magnets, beside its use in cryogenics and ultra high vacuum technology [1]. Iron holds promises as a constituent element in the ß-FeSi2 material to be applied in new opto-electronic devices [2] and it is currently used, together with chromium and manganese, in the production of special magneto-optical materials for digital recording. The use of ultra high purity manganese and chromium in semiconductor technology is evolving. Although not considered a transition metal, zinc is also treated here because of the major significance in compound ZnSe semiconductors [3], and the possibility to purify it by the anion exchange method."

Jan 1, 2000

By Daoxin Wu

In this paper, the rutile TiO2 were prepared under air, Ar and H2 calcination atmosphere by low temperature hydrolysis using Tetrabutyl titanate (C16H36O4Ti) as raw material. Powers were characterized by X-ray diffraction, UV-vis diffuse reflectance and X-ray photoelectron spectroscopy. The influence of the calcination atmosphere on the photocatalytic reactivity of rutile TiO2 for oxygen production was investigated. The photocatalytic reactivity of rutile TiO2 prepared under air, Ar and H2 atmosphere was compared under ultraviolet and visible light radiation with Fe3+ (c=8.0mmol.L-1) as electron acceptor. The results showed that rutile TiO2 prepared under Ar and H2 atmosphere had higher photocatalytic activity for oxygen production than that prepared under air atmosphere. The oxygen production rates under ultraviolet irradiation were 427.5, 378.2 and 357.0µmol.l-1h-1 respectively when rutile TiO2 was prepared under Ar, H2 and air atmosphere. The oxygen production rates under visible light irradiation were 78.2, 52.2 and 13.5µmol.l-1h-1 respectively when rutile TiO2 was prepared under Ar, H2 and air atmosphere.

Jan 1, 2008

By S. Aguayo-Salinas, J. L. Valenzuela-García, A. L. Leal-Cruz, M. I. Pech-Canul, M. T. Certucha-Barragán

"The aim of this research was to carry out a comparative and systematic study of the degradation of cyanide by hybrid natural/biodegradation and biodegradation methods using a mixture of Pseudomonas sp and Bacillus megaterium native bacteria. Bioreactors consist of filled columns with contaminated ore containing 100 ppm of total cyanide. In the biodegradation tests a mixture of bacteria was inoculated into the biodegrading solution. Results of cyanide degradation show a similar asymptotic behavior in both the hybrid (opened system) and biodegradation (closed system) methods; however, for the same period of time (72 h) the permissible maximum levels (1-2 ppm of cyanide) are only attained in the closed system. While in the closed system the cyanide levels are reduced from 100 to 1.5 ppm, in the open system, cyanide decreases from 100 to 2.4 ppm.IntroductionOne of the most important tasks of mining industry is the treatment of the wastes generated in mining operations. Accordingly, industrial waste waters and ores represent a complex problem and a great challenge. In addition to ethic and communitarian considerations, there are laws that prohibit or regulate the contamination of water and air. Moreover, they establish that the restoration of wastes must be considered as a necessary operation cost [1]. Currently this important problem is being addressed by the mining and metallurgical industries using different approaches; mainly they are focusing on the treatment of waste waters and ores generated by the leaching process in which cyanide is used as a leaching agent for the recovery of precious metals as gold and silver. Cyanides have toxic characteristics and thus negatively impact the environment when they are discharged to the ground without previous treatment. While there are some processes in current use there are others that have only been proposed and that allow cyanide degradation, transformation to less toxic compounds and/or the complete elimination of cyanide. The second group includes a variety of techniques that use natural, chemical and biological treatments. Natural treatments consist of the passive abandoning of the heap and of its washing with water. Since these processes are slow and generate great volumes of water partially contaminated, then other alternatives should be considered."

Jan 1, 2008

By Maria Margarida Lima, Maria Lucelinda Cunha, Dora Algarvio

"The main goal of the present work is the quality improvement of the recycled aggregates produced by a construction and demolition waste (C&DW) recycling facility located in Montemor-o-Novo, Portugal. The recycling process was developed on a pilot plant scale with 50 t/h of capacity. Process operations are the hammer mill comminution, magnetic separation and screening.In order to improve the knowledge on the C&DW, a characterization procedure was implemented by hand-sorting, magnetic and density separation on representative samples. On the other hand, to improve the quality of the produced aggregates, the bar screen size fractions were analysed, according to the Portuguese Standard (NP EN 933-1 2000).Wood was identified as the critical contaminant, representing 17% by weight of the total contaminants. Sieving results showed that about 97%, 76%, 56%, 98% and 57% were on the correct size range, which lower results are probably due to the type of screens and/or the material characteristics of the recycled aggregates.IntroductionThe construction and demolition waste problemConstruction and demolition waste (C&DW) is generated by the construction activity, resulting from both, buildings or other structures construction and old structures demolition. As a reference, it can be told that C&DW comprises about 40 to 50% of rubbish (concrete, asphalt, bricks, blocks and dirt), 20 to 30% of wood and related products and 20 to 30% of miscellaneous wastes [1]. In Portugal, C&DW is classified in the LER (Portuguese nick name for the European Waste List), Chapter 17, and includes a diversity of wastes, like concrete, bricks, ceramics, bricks, wood, glass, plaster, copper, zinc, lead, iron, steel, as well as insulation and roofing materials. C&DW stream has several characteristics which make it particularly difficult to deal with and are summarized in the following five items.(1) Lack of information on quantities generated: In Portugal, the C&DW sector has been neglected over the past years, which meant that there are not consistent information concerning the quantities and composition of these wastes yet. Several estimates, based in different assumptions, indicate different results, which may vary from 219 Mt to 10 931 Mt [2]."

Jan 1, 2008

By M. Misra

The finely dispersed kerogen particulates present in the dilute suspension can be coagulated with the aid of a hydrophobic organism, Mycobacterium Dhlei. The initial coagulation and aggregation are strongly dependent on pH and organism concentration, the isoelectric points of oil shale kerogen and Mycobacterium phlei are at pH 3 and 1.8 respectively. As a result the aggregation is rapid around pH 3. Preliminary results show that it is quite possible to use microorganisms for enhanced dewatering of kerogen concentrate produced by froth. flotation.

Jan 1, 1991

By Toshiro Kuji, Masakazu Fujita, Tetsuji Saito

"The magnetic properties of the magnetic materials were deeply dependent on the microstructures. In this study, the novel technique to produce the desired microstructures in a controlled manner was proposed. The technique consisted of the production of the amorphous alloys and the control of the crystallization process. The technique was applied to improve the magnetic properties of Nd-Fe-B permanent magnets. The microstructural control of the magnets exhibited the excellently high energy-products of higher than 430 kJm-1. The relationship between the magnetic properties and the microstructures of the Nd-Fe-B permanent magnets was discussed.IntroductionThe intrinsic properties of the materials are basically determined by the properties of the constituent elements or the compounds. However, it is often noticed the difference between the observed properties and the theoretical values expected from the intrinsic properties of the materials. This indicates that the observed properties of the materials are determined not only by the properties of the constituent elements. In other words, the observed properties of the materials are also strongly dependent on the morphology of materials. This means that the microstructural control may creates a great improvement of the properties of materials.In Nd-Fe-B permanent magnets, the superiority arises from the uniaxial intermetallic Nd2Fe14B compound which has a large saturation magnetization and a high anisotropy field [1,2]. The magnetic properties of the Nd-Fe-B permanent magnets are dependent on the microstructure, that is, the size, shape and degree of the crystallographic alignment of the Nd2Fe14B phase. Currently, the Nd-Fe-B permanent magnets have been produced by either sintering or melt-spinning [3,4]. In the sintered magnets, alignment of the Nd2Fe14B phase is achieved by the prior green compaction of the crushed ingot powders in an applied magnetic field [3]. In the melt-spinning approach, alignment of the Nd2Fe14B phase is achieved by hot deformation [5]. Amorphous melt-spun ribbons are comminuted and then are consolidated into bulk form by hot pressing before hot deformation. As-hot-pressed magnets have randomly oriented Nd2Fe1~ grains [6]. Subsequent die upsetting of as-hot-pressed magnets gives rise to the crystallographic alignment of the Nd2Fe14B phase."

Jan 1, 1998

By Hideaki Tokuyama

Recovery of Ni from acidic wastewater of metal surface treatment has been investigated for reuse of the metal and water. Ion exchange equilibria between Ni ion and a strong acid cation resin, DIAION SKIB, and effective diffusivity in resin particle have been studied and they related to the concentration of HCI. The amount of adsorbed Ni for unit quantity of resin decreases with the increase in HCI concentration. This trend is remarkable for acid concentration above 0.1 kmol/m3,. The exchanging ratio of Ni2+ to H+ in resin particle is I/2 and the values of equilibrium coefficient K and maximum exchange capacity Q are I.62 and 3.16 keq/m3 -dry resin, respectively. Effective diffusivity D. determined from the observed breakthrough curve increases with increasing concentration of DC!. A prototype of moving bed has been developed and applied for the recovery of Ni from model solutions of wastewater prepared by mixing HCl and NiCl2. This apparatus allows us to control the resin flow rate by changing the cross sectional area of hole I the Teflon plate installed at the bottom of resin bed. Characteristics of Ni recovery have been clarified under various liquid flow rates. In any case for Q1, Ni ion has been effectively recovered on SKIB resin and the removed fraction was more than 99.5 %. Higher loading ratio of ion is attained at larger liquid flow rate.

Jan 1, 2003

By Tangstadm Merete, Eli Ringdalen

"This paper presents an overview of results from The Norwegian Research Institution SINTEF and the Norwegian University of Science and Technology, NTNU regarding new and ongoing research in silicon production. The main studies are related to condensation of SiO gas and cavity formation. If SiO gas condensation is increased at the top of the furnace resulting in SiO content in the off-gas closer to equilibrium, the Si yield will be increased significantly. Experimental work, simulating a cavity under industrial conditions, has shown that the cavity grows downwards from one layer. Physical appearance of zones in industrial furnaces, and selected reactions in these, are discussed based on results from excavation of industrial furnaces and results from laboratory experiments. Experimental studies of reaction rates for the formation of SiO are presented. Quartz properties are demonstrated to vary between differing quartz types and the effect of this is discussed.Introduction Both the theoretical and industrial issues associated with the production of silicon are described in detail in the textbook written by Schei et al [1]. This book covers the knowledge of silicon production process up to 1998. Together with the work by Myrhaug [1] and by Aasly[2], this is the main basis for this paper. Recent and ongoing research at SINTEF and NTNU focusing on production of Si and SiO in the high temperature zone, dissociation of SiO and condensate and cavity formation will be discussed."

Jan 1, 2012

By A. V. Tarasov, S. D. Klushin

493 The most common method for minimizing the copper content of residual slag in the process of autogenous smelting of sulfide raw materials is treatment of molten slag in an electric furnace, with optional addition of solid reducing agents, such as coke, and/or sulfiding agents such as pyrite. A drawback of this technique is the fact that the final slag produced still contains 0.5% or more Cu. We have tested a method for treating molten slag obtained as a result of autogenous smelting by a gaseous mixture of sulfur dioxide and methane at a ratio of. SC:SO2 = 0.75 :1.0 in the presence of oxygen. Interaction reaction within the SO2-O2-CRi system proceeded at a high rate at 1373 to 1573 K to form reducing and sulfiding agents: H2S, S, COS, CO, CO2, H2, H2O. The gas mixture requirement was about 100 to 150 Nm3 per 1 tonne of slag. A decrease in the ferric iron concentration (Fe3+) from 10-15% down to 2-3% resulted in lower solubility of copper in slag, and agitation of the melt with gas stream accelerated. the separation of the sulfide phase and slag. Removal of copper from slag was performed in a pilot unit within the second V anyukov furnace zone where slag arrived with a copper content of 0.8-1.3%. The temperature of molten slag was maintained within 1523 to 1573 K. The copper content of the final slag was at a level of0.12 to 0.14%. The matte sent to converting was a mixture of bottom matte from the smelting zone and the slag treatment zone. It had a copper content of about 50 to 55%. Process gases from both furnace zones were combined and sent to the acid plant for sulfur recovery. This process was offered for commercial use at two copper smelters in Russia and CIS.

Jan 1, 2000

By Toyohisa Fujita

The effect of variables on the gold extraction with ammonium thiosulfate was investigated on sponge gold and ore samples. The Effects of CUS04, (NH4hS203, NH40H, (N~hS04' pH, stirring speed and retention on gold leaching rate and thiosulfate oxidation (consumption) have been studied. Almost 100% of gold was leached from sponge gold and over 96% from ore sample at optimum conditions. Trioctylmethyl ammonium chloride was used to recover gold from thiosulfate pregnant solution. It was found that more than 99% of gold was recovered by the extractant diluted with n-octane at 01 A ratio of 1: 1 without the re-adjustment of pH or others. Also, the gold cementation was conducted without de-aeration by using zinc, copper and aluminum powders. The result indicated that the gold was effectively recovered from a solution of low ammonia and copper concentrations and higher thiosulfate concentration. The gold recovery process by using ammonium thiosulfate is an environmental friendly method comparing to conventional cyanidation process.

Jan 1, 2003

By Katsunori Yamaguchi

The zinc, lead and alumina contents in copper smelting slag are increasing with the increase in waste recycling. The recovery of base metals such as lead and zinc from copper converter slag is important from both an economical and environmental perspective. As a fundamental study of the metal recovery by reduction process, activity coefficients of ZnO and PbO in the CaO-SiO2-FeOx-5mass%AlO1.5 slag under iron saturation at 1573K are derived from the data of slag-metal equilibrium experiments. On the basis of the obtained data, the activity coefficients of ZnO and PbO in the CaO-SiO2-FeOx-5mass%AlO1.5 slag were compared with those of the CaO-SiO2-FeOx ternary system. Addition of alumina increases activities coefficient of ZnO and PbO in SiO2 rich side of the slag, and decreases them in CaO rich side.

Jan 1, 2006

By Xi Dai

The LiFe1-xNixPO4(x=0, 0.05, 0.10) cathode materials for Li-ion battery were synthesized with Fe1xNixC2O4?2H2O(x=0, 0.05, 0.10) as Fe sources by high temperature solid-state reaction method. The Fe1xNixC2O4?2H2O(x=0, 0.05, 0.10) materials were produced by liquid co-precipitation method and crystal structure and morphology of cathode materials were characterized by X-ray diffraction and scanning electron microscopy. The composition contents and charge-discharge performances were measured by chemistry analysis and charge-discharge apparatus. The XRD patterns showed that LiFe1-xNixPO4(x=0, 0.05, 0.10) cathode material samples were well-crystallized homogeneous olivine-type phase, with only tiny trivalent iron impurities according to chemistry analysis results. Charge-discharge test showed that cathode materials possessed excellent charge/discharge capacities, about 150mAh/g at 0.1C rate and more than 120mAh/g at 0.4C rate. The polarization of cathode in charge-discharge process can be restrained effectively, for the potential offset between oxidative peak and reductive peak of doped LiFePO4 material was only 0.079V, lower than pure LiFePO4 markedly.

Jan 1, 2006

By Hai-Peng Guo, Lu Jiang, Xiao-Man Yan, Bing Xie, Hong-Yi Li

Traditional, calcium compounds cannot be used in vanadium extraction processing due to the limitation of sodium roasting technology, which results in unsatisfied dephosphorization for vanadium-containing hot metal in converter and thus increasing the dephosphorization burden for subsequent steelmaking. The calcium roasting technology is an alternative for vanadium extraction and allows adding lime into vanadium slag in converter. In the present study, vanadium was leached by soda from roasted vanadium slag with high calcium content. Effects of roasting temperature and time, leaching temperature, Na2CO3 concentration andliquid to solid ratio on vanadium leaching rate were studied. The results show that 94% of vanadium was extracted by roasting the vanadium slag at 950℃ for 2.5h and then leaching in 160g/L Na2CO3 liquid at 95℃ for 1h with liquid to solid ratio of 10:1 ml/g. Impurities of Si and P reacted with calcium and formed insoluble Ca2SiO4 and Ca3(PO4)2 respectively.

Jan 1, 2015

By J. Wendt, P. R. Sahm, T. Uloth, M. Weck, F. Foertsch

"The FEM program systems CASTS (Computer Aided Solidification TechnologieS) (1) and FINELF (FINite ELement Frontal Solver) are used to optimize a thin walled die casting. After a short description of the programs it will be worked out how to use them not only for simulating solidification processes but also for optimizing the design of workpieces. The calculations will be done for an automobile's support bracket which is manufactured in a well known car factory in Stuttgart, FRG.IntroductionAt the Aachen Foundry Institute the software package CASTS was developped to simulate solidification of castings. In order to optimize the whole manufacturing process it does not appear sufficient any more to take into account only the specific aspects of casting. For instance one has to consider additionally the stress situation under service load. For this reason the Foundry Institute together with the Aachen WZL-Institute (Machine Tool Laboratory) and the car factory mentioned above started to probe into a first step in that direction. Figure 1 shows the support bracket which shall be optimized."

Jan 1, 1986

By Tae-Hyun Kim, Kang-In Rhee, Jeong-Soo Sohn

The synthesis of Mn-Zn ferrite powder from spent zinc-carbon batteries was investigated using a series of physical treatment, sulfuric acid leaching and coprecipitation. Physical separation methods such as crushing, magnetic separation and sieving were applied to generate a non-magnetic material of 8- mesh undersize for subsequent leaching process. The 8-mesh undersize of the spent zinc-carbon batteries was assayed 23.9% Mn, 14.9% Zn, and 4% Fe. Metal extractions obtained in sulfuric acid leaching at the solid/liquid ratio of 1:10, 2 M H2SO4, and 60? with 6 vol.% H2O2 addition were 97.9% Mn, 98.0% Zn and 55.2% Fe. The leach liquor was finally adjusted to the Mn:Zn:Fe mole ratio of 1:1:4 suitable for producing MnZnFe4O8 ferrite powder by the addition of Mn, Zn and Fe sulfates followed by pH control. A co-precipitation test for Mn-Zn ferrite powder was performed at 80?, O2 gas flowing at 1.3 L/min. As a result of co-precipitation, Mn-Zn ferrite nanoparticles in 20 nm size with spinel structure were successfully synthesized. The saturation magnetizations of Mn-Zn ferrite powder (Mn1-xZnxFe2O4) were determined to be 39-91 emu/g with various zinc contents (X=0.2-0.8).

Jan 1, 2008

By Hua Hou, Xiaofeng Niu, Wei Liang

"The explicit finite difference (EFD) method is used for calculating the casting temperature field during solidification. Because the time step is limited, the computational efficiency of the EFD method is lower. In order to improve the computational efficiency, a fourth-order in space and second-order in time model based on the equivalent specific heat method and the alternating direction implicit (ADI) method is established. The degree of similarity between the simulation results and the experimental results is analyzed. The results show that the simulation results of this high order mathematical model are close to the experimental results.IntroductionThe 3D heat transfer equation of temperature field during solidification process is as the following: [1-3]."

Jan 1, 2013

By Ibrahim Yusufoglu, Ahmet Orkun Kalpakli, Cem Kahruman, Sedat Ilhan

"The effects of oxalic acid concentration, temperature, stirring rate and particle size on the dissolution rate of synthetically prepared calcium molybdate were investigated. Dissolution of calcium molybdate in oxalic acid solutions takes place as a series - parallel type reaction. In the first reaction step, which proceeds according to the ""Langmuir - Hinshelwood Mechanism"", calcium aqua oxalato molybdate is formed as a complex chelate intermediate product. In the second reaction step, molybdic acid is formed during the slow hydrolysis of calcium aqua oxalato molybdate, and it reacts rapidly with oxalic acid to form the polymeric hydrogen oxalate dimolybdate chelate as an end product. Activation energies were calculated as 41.4 and 49.9 kJ mol-1 for the first and zero order reactions. The fractional conversion versus time relationship can be given by the following equation.IntroductionMolybdenum is used widely in electric-electronic, metal working, aerospace and aeronautic, nuclear, glass and petrochemical industries because of its high melting temperature and resistance against chemical effects. However, the largest molybdenum consumers are the iron-steel and super alloy industries where molybdenum is used as an alloying element. Industrially important molybdenum minerals are limited to molybdenite (M0S2), powellite (CaMo04) and wulfenite (PbMo04), which are considered as primary molybdenum resources. Secondary molybdenum resources are spent catalysts and scrap [1-4].Molybdenum has been produced by pyrometallurgical processes in the past. Since it is possible to process low grade molybdenum ores and industrial wastes by hydrometallurgical processes, which are more environmentally friendly than pyrometallurgical processes, the importance of the use of hydrometallurgical processes has increased in the molybdenum production industry."

Jan 1, 2012