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By S. -H. Jeon, Y. -S. Choi

"The three dimensional current distribution on the rectangular cathode is predicted using a boundary element method with a linear element of trigonal type. The effect of cell geometry and anode shape on current distribution is simulated. Calculated results compare well with experimental results. The proper combination of anode size and distance between electrodes increase the current uniformity.The importance of electrodeposition as a fabrication technology in the electronics industry is large and growing. The main advantages of this wet processing method, in comparison to other dry processing methods, lie in its high yield, rapid processing and low cost. In nearly every application of electrodeposition the pursuit of deposit uniformity, especially thickness uniformity, has been technically imperative. The thickness uniformity of the deposit depends largely on the current distribution over the cathode. The current distribution is primarily determined by the geometrical characteristics of the electrodes and the cell. Also the polarization at the electrode surface and the mass transfer affect the current distribution.The current distribution is an important consideration for those involved in designing electrochemical systems and electroplating systems in particular. Although it is important, the common practice in industry is to use trial and error method to design the cell that optimize the uniformity of current distributions in electroplating. The purpose of this paper is to illustrate the useof boundary element method to predict three-dimensional current distribution in rectangular cell.The calculation of the current distribution is possible by various numerical techniques, which include the finite difference method (FDM)1, the finite element method (FEM)2, and the boundary element method (BEM)3,4. These methods of the numerical calculation have various problems, respectively, but the BEM is considered to be the most efficient. This is due to the fact that the BEM has the advantage of solving field equations only on the surface of a calculation domain. A good comparison between the BEM and the FEM for the secondary current distribution in a Hull cell was made by Matlosz et al.5The fundamentals on the theory of current distribution in electroplating are well-established in the literature by a number of authors.6, 7, 8 However, a small fraction of these works have been specially addressed to three-dimensional analysis, and, mostly thel·10 have focused on the problem qualitatively rather than quantitatively.Extending the previous work to three-dimension, we developed the program for the quantitative calculation of 3-dimensional current distribution using a boundary element method with a linear element of trigonal type. Integrals with singularity from the fundamental solution have been analytically computed and it is shown in detail in the Iiterature11. This paper deals with the three dimensional current distribution for the electrode position of copper in a cubic type cell and the effect of anode shape, size and the distance between electrodes on current distribution is studied."

Jan 1, 1997

By Ali Unal, Ali I. Kahveci

Alcoa developed a fractional crystallization process some 30 years ago as a method to purify aluminum. Depending on the purity of feed metal, it has been commercially used to make 3N7-6N purity aluminum. As an extension of this technology, Alcoa has experimented with purifying various aluminum alloy scrap for the purpose of recycling. Purified aluminum alloy scrap can be reused for making the same alloy. This presentation will discuss Alcoa fractional crystallization technology and its application to alloy scrap processing. Process capabilities and the partitioning of eutectic and peritectic impurities during fractional crystallization will be discussed for the alloy systems investigated.

Jan 1, 2000

By Lauri Pajunen

DSA-anodes are widely used in metal electrowinning. In zinc electrowinning the electrolyte solution contains manganese ions, and the deposition of manganese dioxide happens on the anode. This manganese dioxide layer cannot be removed without losing the active coating of the DSA-anode. The same problem can be found with hybrid anodes. In hybrid anodes mixed metal oxide coated titanium mesh is attached to a lead base material. In this study, the effect of dissolved manganese on anode behaviour is studied with three different anodes. These anodes are lead anode with 0.6% silver, hybrid anode and DSA-mesh. Methods of study include polarization, galvanostatic and potential mapping experiments.

Jan 1, 2003

By Min Chen, Zhen Tian, Hongxu Cui

"The effects of adjusting technology on the phosphorous enrichment in converter slag were investigated. The results showed that the grain size of 2CaO·SiO2 with high phosphorus containing content increased slightly with the decreasing of cooling rate, and the proper cooling rate was confirmed to be about l.0°C.min-1. Moreover, the morphology of the phosphorus-rich phase of 2CaO·SiO2-3CaO·P2O 5 was changed from granular for the higher basicity of converter slag to the coexistence of granular shape and rod-like for the lower basicity of adjusted slag. With the addition of adjusting agent such as SiO2 to lower the basicity of converter slag, the phosphorus in converter slag could be transferred into 2CaO·Si02 phase effectively, and P2O 5 content in high phosphorus containing phase reached to above 30%.IntroductionThe yield of converter slag is very large in China, but most of the slag is stacked usually after the separation of iron, which not only takes up a lot of land, but also affects the ecological environment seriously. Therefore, improving the comprehensive utilization and value-added products of converter slag is of great significance to recycle the steelmaking slag[l-3]. On the other hand, the refining of hot metal with high phosphorous content is an unavoidable problem with the decreasing of high grade iron ore, and as a result, more amounts of high phosphorus containing steelmaking slag are produced. However, the current recycle of converter slag is more focused on the emission reduction and reuse of steelmaking slag inside the iron and steelmaking process without considering the recycle of phosphorous resources[4-6]. At the same time, the development and utilization of phosphate ore as a strategic resource is drawing more and more attention, but the phosphate ore in China is mostly low grade and significant amounts of tailings are produced which is harmful to the environment. Therefore, it is important to separate phosphorous resources in steelmaking slag which can be used as phosphate ore for fertilizer material[7-9].Literature studies showed that most of the phosphorus in steelmaking slag existing as 2CaO·SiO2-3CaO·P2O 5 solid solution phase in 2CaO·SiO2 particle. The P2O 5 content in the phosphorus containing phase is very low due to the fact that the basicity of converter slag is usually high and the precipitated amounts of 2CaO·SiO2 particles during cooling are very large, resulting in the fact that the P2O 5 contents in 2CaO·SiO2-3CaO·P2O 5 solid solution phase are much lower which is impossible to be used as phosphorous resources instead of phosphate ore. Thus, the enrichment of phosphorus in steelmaking slag is need[ 10-14]."

Jan 1, 2011

By Goren Lindkvist

Elkem has a small industrial scale. Muti-Purpose furnace at the MEFOS Metallurgical Research Facility in Lulea, Sweden. The furnace is 2 meters in diameter with installed power of 4.8 MVA, equipped with oil coiled freeze lining, gas tight electrode seals and feed chutes and a slag flow control for continuous tapping. During tests in June, 1991, the furnace was continuously operated on a high silica slag at loads from 1.5 to 4,0 MW. The slag was then charges to a low silica, high iron and lime composition. Steel plant dust was added, smelted and reduced. The slag was made more ceramic by adding alumobrick and alumina. Data from the start-up and initial operating phase of the, Elkem EAF dust plant at Laclede Steel will also reviewed.

Jan 1, 1992

By V. B. Telles, D. C. R. Espinosa, J. A. S. Tenório

"The purpose of this work was to study the reutilization of the steelmaking dust, derived from steel production in the electric arc furnace (EAF), in iron ore sintering process aiming zinc elimination. In each sintering process were collected sintered samples, these materials were analyzed by chemical analysis using atomic absorption spectrophotometry in order to determine the zinc content. Samples of not sintered mixtures were also characterized by chemical analysis aiming to determine the initial amounts of zinc, i.e. in order to check the zinc amounts present in the mixture before the sintering process. The comparation among the zinc contents of samples sintered and not sintered allowed to determine the elimination of zinc during the experiments. Results showed that the zinc elimination in the process is proportional to the ratio reducer/waste. The zinc removal was lower when the reducer/waste ratio was decreased.IntroductionThe electric arc furnace dust (EAFD) is a residue generated in the steelmaking process using electric arc furnace. Aproximately 30% of all steel produced (in the year 2009) was obtained through electric arc furance (EAF). In the United States of America the percentage of this process in the total crude steel production was about 62% in 2009, while in 2000 this percentage was only 47% [1].The iron ore sintering is a process that reuses wastes generated in metallurgical industries. However, the materials used must be physical and chemical characteristics compatible with the blast furnaces.The quantity of zinc, cadmium, chrome and other metals present in the EAFD depends on the quality of the scrap used to feed the EAF and the type of steel that it is been made [2,3]. The reuse of EAFD waste is interesting to steelmaking processes because of its iron content. However the presence of zinc inside a blast furnace is undesirable since the zinc oxide can be deposited on the blast furnace walls and in the drivers of gas output, interrupting the flow. Another part of the zinc oxide can form deposits on the refractory lining of the blast furnace [4,5]."

Jan 1, 2012

By David G. Dixon, Ahmad Ghahremaninezhad, Edouard Asselin

"In this study pertaining to the electrochemistry of chalcopyrite, the active/passive behavior of a chalcopyrite electrode in 0.5M sulfuric acid solution was investigated. Potentiostatic and potentiodynamic polarization and multi-cyclic voltanunetry were conducted to analyze the electrodissolution parameters of the electrode.The potentiodynamic and potentiostatic polarizations of chalcopyrite revealed the formation of a passive film on the surface of chalcopyrite. From the potentiostatic study in the passive potential region, a decrease in the dissolution current density by increasing the potential was observed. From this, it was concluded that the passive film is an n-type semiconductor and cation interstitial defects or anion vacancies are the charge carriers. From multi-cyclic voltammetry studies, four cathodic peaks at - 0.37, 0.30, -0.10 and-0.20 YsHE were detected on the surface of a passivated chalcopyrite electrode. The cathodic peaks at 0.37 and 0.30 V were connected to ferric to ferrous reduction and copper sulfide formation, respectively. The peaks at -0.10 and - 0.20 were related to chalcopyrite reduction. The products of the chalcopyrite reduction reactions were suggested to be Cu2S, Cu9fesS16 and Cu5feS4 and evolution of hydrogen sulfide gas (H2S).IntroductionChalcopyrite is the most abundant copper bearing mineral in the world and its dissolution behavior represents the most important technological consideration in the hydrometallurgical extraction of copper [I]. Since the current pyrometallurgical methods for copper extraction from chalcopyrite have environmental issues, many studies have considered the leaching and dissolution of CuFeS2 in different aqueous media [2-5]. The main problem associated with leaching processes is the slow dissolution rate of the mineral [6]. During the dissolution process, increasing the potential of the chalcopyrite in the anodic direction will cause the formation of surface layers which hinder the dissolution rate of the mineral [7]. The precise composition of the layers is in dispute. Previous studies have concluded that these layers could be sulfur [8-9], precipitated iron compounds [8], a solid electrolyte interphase (SEI) - which slows the rate of electron transfer- [10], a metal deficient sulfide [ll], or polysulfidic in nature [12-13]. In order to increase the leaching kinetics of chalcopyrite, the characterization of the layers formed during dissolution is essential and electrochemical methods are important to this end. Studies by Biegler [14] show nucleation and growth of a thin two-dimensional sulfide phase on the surface of chalcopyrite during the exposure of a polished sample in HzS04 solution or air. More studies by Biegler and Swift [15] have shown evidence for nucleation and growth of a 3-dimensional phase at low anodic potentials (around 200 mV vs. OCP). The current-time behavior of the dissolution process in this potential area has the characteristics of expansion and overlap of localized dissolution centers."

Jan 1, 2012

By Sung Jin Han

Magnesia-based refractory is generally used in an electric arc furnace (EAF) due to its relatively high corrosion resistance and strength at high temperatures. However, the magnesia refractory is attacked by EAF slag and thus the lining life continuously decreases. Thus, it is significant to identify the interfacial reaction between magnesia refractory and FeO-rich EAF slags. In the present study, the influence of FeO-rich slag on the corrosion behavior of MgO refractory was evaluated. The (Fe,Mg)Oss layer was observed at the slag-refractory interface and its thickness increased with increasing content of FeO in the slag. The specific reaction phenomena and formation behavior of (Fe,Mg)Oss layer were evaluated by thermochemical computing program, FactsageTM7.0.

By Alessandra Bonoli, Garfìm Marianna

"Construction and demolition waste (CDW) is no dangerous material resulting from construction, and demolition of houses, large building structures, roads, bridges, piers, and dams. It is possible to recycle these materials, to reduce environmental impacts, and to reuse them in construction sector. To evaluate in a correct way the possibility to reuse this material it is important to lead laboratory tests to assess the proprieties and quality characteristics. European, Italian and British ad hoc Committees had elaborated specific Standards, to evaluate Geometrical, Physical, and Chemical requirements of recycled materials. A research was carried on to define the guidelines for laboratory tests, their suggested values and quality standards. The Construction and Demolition Waste Construction and demolition waste (CDW) is no dangerous, uncontaminated material resulting from construction, renovation, repair, and demolition of houses, large building structures, roads, bridges, piers, and dams. CDW waste is made up of wood, steel, concrete, gypsum, masonry, railway ties, roofing materials, carpeting, insulation, plaster, metal, and asphalt, and all waste included in CER Code 17. In particular Demolition wastes are defined as materials resulting from the demolition, instead Construction wastes are defined as waste materials resulting during construction process or in pre-manufacturing construction industry. Environmental problems In a lot of cases Construction and Demolition Waste materials were discharged in landfills, these are filling up with CDW and others, and some of them will close in the near future. In addition, illegal dumping of CDW debris can result in future health risks, decreased property values, cleanup costs and enviromental problems. The typical environmental impacts generated by CDW dumps are: 1- Dust problem, which causes air pollution, as will as forming dirty areas. 2- Uncontrolled locations, that will encourage the disposal of other waste types with the usual construction wastes leading to an environmental disaster. 3- The degradation and deterioration of the coastal lands and the natural protectorates. 4- The loss of aesthetic features. 5- Occupation of large areas, causing extra hauling costs. Therefore, it is wise to find other alternatives, like reuse or recycling, other than landfilling CDW debris or illegal dumps, because a proper management and the reduction of CDW amount can save money, conserve resources, and preserve the environment."

Jan 1, 2008

By Munetaka Iwasaki

Nitrogen strongly affects mechanical properties of steel and therefore we may sometimes modify the various processes for its content. Numerous studies based on the results of chemical analysis of quenched samples were reported with a few exceptions of Hot Sievert method. The technique always poses a risk of uncertainty whether the true content of nitrogen in liquid metal is measured or not. In this study vacuum remelting under relatively low pressure was done to enhance gas phase mass transfer. Total pressure of the melt chamber was about 10-3 pa and electron beam heating was used. Mass spectroscopy was used for the direct observation of the rate of denitrization. Nitrogen molecules or atoms were detected by a mass spectrometer set above the melt. Continuous monitoring of the intensity of the fixed mass number may reflect the transfer of nitrogen from the melt to the vacuum. The results of the new and conventional techniques agree, both technique can be verified.

Jan 1, 1999

By G Hope, C Young, R. N. Gow

"The presence of enargite (Cu3AsS4) is problematic in gold processing as it is refractory, increasing cyanide and oxygen consumption, and enviromnentally hazardous. Selective leaching and treatment of the arsenic would prove advantageous to conventional gold leaching methods. The reactivity of enargite samples from Montana, US and Quiruvilca, Peru were studied under alkaline conditions, pH range of 8-13, using a cyclic voltammetry corrosion cell setup. Raman spectra of the surface were taken during and after cycling to compare surface species against theoretical predominance diagrams. Under slightly oxidizing conditions, covellite (CuS) peaks were found on the surface in a short matter of time, above - 200m V vs SHE for pH 9-13, suggesting arsenic leaching, but for longer conditioning times, elemental sulfur peaks were also found, which created a passivating surface layer. By operating above pH 12, under reducing conditions, ~-500mV vs SHE, arsenic can be leached as a thioarsenate (AsS4-xOx3-), without sulfur formation.IntroductionEnviromnental limitations on pyrometallurgical processing of arsenic has pushed the desire to process enargite-, Cu3AsS4, bearing concentrates towards a hydrometallurgical solution. Attempts to process can be broken down into two categories - the co-dissolution of arsenic and copper under acidic conditions or the selective leaching of arsenic under basic conditions. The selective leaching of arsenic would preferably leave behind a chalcocite, Cu2S, or covellite, CuS, phase that would be more amenable to conventional processing methods of the copper and gold industries. These methods employ bi- or poly-sulfides to leach arsenic as Assl· [1-4], hypochlorite leaching [5-7], ammoniacal leaching [8] or fine grinding to mechanically activate the enargite surface and increase normally slow reaction kinetics[9]. This study looked into the surface formations of an enargite electrode under alkaline conditions, in a pH range from 8-13, as it cycled from -1000 mV to 1000 mV vs SHE. The understanding of the formations and under what conditions they form will be helpful in further development of any of the aforementioned processes."

Jan 1, 2012

By Zhanjun Wang, Yongqi Sun, Mei Zhang, Zuotai Zhang, Min Guo

The role of fluorine on the viscous and crystallization behavior of CaO-SiO2-MgO-Al2O3-FetO-P2O5-(CaF2) slags were explored using the rotating cylinder method, non-isothermal differential scanning calorimeter (DSC), X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. It was found that the viscosity slightly decreased with increasing CaF2 content. It was also found that CaF2 addition can promote the primary phase transformed from MgFe2O4 spinel to Ca3(PO4)F, which was beneficial to the enrichment of phosphorus. Additionally, the structure of the slags explained by X-ray photoelectron spectroscopy (XPS) and magic angular spinning nuclear magnetic resonance (MAS-NMR) were further analyzed, which was well in accordance with the above analysis.

Jan 1, 2016

By S. Suda

Hydrogen storage materials have been investigated for more than 30 years, particularly on metal hydrides. These materials are, however, considered today impractical because of their poor hydrogen capacity measured by mass density and their poor surface properties and characteristics against impurities. Recent R&D activities have been located in new categories of materials such as complex hydrides and chemical hydrides. Among these materials, NaAlH4 (one of alanates), Li-based complex hydride, and NaBH4 (SBH: sodium borohydride) are 3 major candidates as hydrogen storage materials. In the presentation, SBH as a non-reversible on-site but recyclable off-site is described in view of its practical availability as the source of H- (protide) applied for a new type of fuel cell named Direct Borohydride Fuel Cell (DBFC) and H2 (hydrogen) for Proton Exchange Membrane Fuel Cell (PEMFC).

Jan 1, 2006

By Hal dun Kurama

In thus-study, Bigadic upper zone zeolitic tuff, which contains about 87% clinoptilolite was used as an ion exchanger for removal of Pb++, Cu++, Cd++ and Hg++ ions from wastewater. Bench scale experiments with two different glass columns, were carried out continuously under the closed/ open circuit conditions. Before ion exchange tests, zeolite samples were treated with NaCI (6ml/ min. and 42BV). The effects of particle size, bed volume, pH and flow rate on the ion exchange capacity were determined. Under the best operation conditions, the effect of initial influent solution concentration on ion exchange selectivity was tested. As a-result, it was found that the Bigadiç clinoptilolite had the following ion exchange capacities;

Jan 1, 1995

By J. N. Hryn

This paper describes some of the work done in Phase 1 of a multi-year, five-phase program aimed at demonstrating the economic feasibility of producing commercial-scale quantities of commodity materials derived from salt cake residue-oxide. The amount of salt cake generated annually in the U. S. is estimated to be 510,000 tons, including 340,000 tons of residue-oxide. Used beverage can (UBC) processing accounts for the majority of residue-oxiae that could be made available for further processing into commercial products. To characterize the composition of residue-oxide. eight residue-oxide samples from various secondary processors were obtained and analyzed. Surprisingly, the composition of residue-oxide was found to be independent of source or alloy family being processed, with? the exception of slightly elevated silicon levels in 3XXand UBC residue-oxide samples. Major phases detected in the residue- oxide were? alumina, spinel, and aluminum hydroxides. Preliminary economic analyses indicated that the refractory market appears to be the best choice for high value-added products produced from residue-oxide with minimum processing. Bench-scale tests indicated that low silicon containing residue-oxide is ready to enter this market, but the elevated silicon content of UBC and 3XX residue-oxide preclude this possibility. A separation technology should 'be developed to remove silicon-containing . species from the alumina and spinel values Present in residue-oxide. This technology would then allow UBC and 3XX residue-oxides to be converted to significantly higher value-added products.

Jan 1, 1995

By Adam Gesing, Paul Marchwica, Jerry Sokolowski, Sharon Lackie

"Often referred to as SEM-EDX, energy-dispersive spectroscopic analysis of characteristic fluorescence x-ray is a standard technique for semi-quantitative elemental composition analysis in scanning electron microscopy. It is quick and extremely useful for identification of phases in the sample microstructure, as long as the constituents are significantly larger than the probe volume from which the fluorescence x-rays originate. The probe volume ranges from a few to several microns, depending on the electron beam spot size and the acceleration voltage. We report on a new variant of an EDX technique developed to overcome this limitation and allow quantitative elemental analysis of smaller phase constituents, down to a size of several nanometers. This variant involves the calculation of compositions of individual phases from multiple analyses of areas containing phases of interest. This significantly increases the usefulness of EDX for quantitative analysis of new nano-structured materials.IntroductionIn any elemental micro-analytical method, the sample material is illuminated by a probe beam that excites an interaction volume of a sample to emit a characteristic signal. This signal in turn interacts with the sample material through absorption and fluorescence mechanisms before a portion of it is collected by a suitable detector and analyzed for elemental composition. The spatial resolution of the method depends on the minimum interaction volume between the probe beam and the sample material.Laser light beams can be tightly focused to a spot size limited by the photon wavelength and can be used to sample the surface of any material. In micro-LIBS (laser-induced plasma spectroscopy) a focused laser beam ablates and vaporizes a small volume of material from the sample surface, creating a plasma spark. Spectral analysis of the light emission from the plasma spark allows the semi-quantitative determination of the elemental composition of the material removed from the sample surface. The smallest reproducible craters achieved are ~ 3mm in diameter and a few nanometers in depth. [l]Particle probe beams of ions or electrons can be focused to a diameter of a few nanometers at the point of impact on the sample. Ions sputter the sample atoms from the point of impact, and the sputtered ionized material is analyzed by mass spectroscopy in a secondary ion mass spectrometer (SIMS). [2] This gives SIMS resolution in a nanometer range. SIMS equipment, however, is expensive and not readily available."

Jan 1, 2013

By A. V. Tarasov

In order to improve the efficiency of hydrometallurgical processing of pyrrhotite concentrates, an integrated set of research has been carried out to investigate the use of sulfur dioxide in individual unit operations and as a leaching agent in the autoclave process as a substitute for oxygen. Treating iron-containing raw materials for production of nonferrous metals are based on the selective reaction of SO2 with iron sulfides and oxides. Iron is dissolved as sulfate, which can be treated in a separate circuit to produce iron-containing pigments or it can be disposed of after neutralization. Nonferrous and precious metals contained in pyrrhotite concentrate do not react with sulfur dioxide and remain virtually completely in the solid phase, i.e. high-grade sulfide concentrate to be treated by hydro- or pyrometallurgical methods. Elemental sulfur formed in the process of leaching is separated from the pulp in granulated form as a result of the use of special surfactants. The process of sulfide concentrate leaching with the use of sulfur dioxide is conducted at temperatures above the sulfur melting point (119°C) with distributed feeding of surfactant and under a partial pressure of sulfur dioxide of up to 0.3 to 0.5 MPa.

Jan 1, 2006

By Q. Chen

The magnetic properties and phase evolution of Nd-lean and/or boron-rich melt- extracted ribbons of Nd98Fe90.2xBx, where x = 6 through 11, have been studied using XRD, DTA, TMA, and VSM. The off-stoichiometric Nd2Fe14B compositions cause additional phases to be present after crystallization and affect the magnetic properties obtained. The crystallization temperature of this alloy series rises with the increasing) boron content. In addition to Nd2Fe14B and a-Fe, Fe3B is detected. It is found that increasing the boron content reduces B, within this composition range. The magnetic properties are directly associated with the relative magnetic phase content in the samples.

Jan 1, 1997

By Daojin Cao

Aiming at many controversial reports on Raman spectral pattern of heptamolybdate ion in aqueous solution appearing in the literature and the absence of its standard pattern, the comparative investigations on Raman spectral pattern of saturated solution of ammonium heptamolybdate tetra hydrate were done. The results showed that the main vibrant frequencies of Raman spectral pattern of the saturated solution were in good agreement with those introduced in the literature, and that the intensity ratio (4.4) of the strongest peak to the second strongest peak recorded in Raman spectrum of the saturated solution had three obvious characteristics: it was greater than each of the results (ranging from 3.7 to 1.3) reported in the literature, much closer to that (4.7) of crystal and well conformed to the change rule of Raman spectra occurring in the process of the first-step polymerization of acidified molybdate solution. It was found that Raman spectrum of heptamolybdate ion in aqueous solution was determined by not only the main vibrant frequencies but also the intensity ratio, which is also the crucial result in this study. The comparative investigations indicate that the pattern of Raman spectrum of the saturated solution is the standard pattern of Raman spectrum of heptamolybdate ion in aqueous solution essentially. The affirmed standard pattern is reliable and can be used to the identification of heptamolybdate ion in aqueous solution, applied in the research of the equilibrium of acidified molybdate solution and the exploration of the best technologic condition for the production of high quality heptamolybdates.

Jan 1, 2006

By Osamu Takeda

A decomposition process for PCBs by using basic molten salts as a reaction field was investigated in order to establish a safe, simple and highly efficient decomposition process for polychlorobiphenyls (PCBs). PCB containing chlorine (e.g. 2, 2?, 4, 4?-tetrachlorobiphenyl) dissolved in n-nonane solution was supplied into basic molten salts (NaOH-Na2CO3 or KOH-K2CO3) maintained at 500-700 ?C together with the carrier gas (N2-21% O2) through an injection tube. The injected PCBs in a bubble are decomposed by the reaction with the molten salts and oxygen during rise in the molten salts. The decomposition efficiency of PCBs increased with increasing temperature and was achieved to be higher than 99.995% in a certain condition. From a series of systematic study, the effectiveness of the decomposition process for PCBs by using molten salts was demonstrated.

Jan 1, 2008