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By Karl-Heinz Daum

Outokumpu Lurgi Metallurgie GmbH, Oberursel, Germany ? give saleable by-products, ? not interfere with smelter performance, ? treat all gas streams simultaneously, and ? comply with environmental regulations. The latest developments in sulphuric acid plant design are presented.

Jan 1, 2002

By Shigehito Isobe

The Li-N-H system composed of LiH and LiNH2 catalyzed by titanium compound desorbs ~6 mass% hydrogen and a quite small amount of ammonia in temperature range from 150 to 250 °C under He flow atmosphere. In this work, hydrogen desorption (H-desorption) mechanism in the reaction from LiH+LiNH2 to Li2NH+H2 in a non-equilibrium condition was clarified by TDMS, TG and FT-IR analyses for the products replaced by LiD or LiND2 for LiH or LiNH2,respectively. The results suggested that H-desorption reaction progresses through two-step elementary reactions mediated by ammonia. As a next step, we carefully determined the amount of the ammonia containing in desorbed hydrogen for the Li-N-H system in a closed system from the practical point of view. The results indicated that a quite small of ammonia thermodynamically coexisted in the desorbed hydrogen in closed system, although ammonia could not be almost detected in emitted hydrogen gas by TDMS under some non-equilibrium conditions. Moreover, for understanding the role of titanium, the chemical bonding state of the titanium compounds doped as catalyst in the mixture was examined by XAFS measurement. The results indicate that the Ti atoms, which can induce catalytic effect, are in a particular chemical bonding state.

Jan 1, 2006

By George Owusu

A study has been carried out on the use of solvent extraction, instead of the traditional zinc dust cementation process, to remove copper from concentrated zinc sulphate leach solutions. In a series of experiments using plant solution containing 1.9 g/L Cu, 2 g/L Fe, 173 g/L Zn, 7.9 g/L H,SO,, 0.25 g/L Cd, 15 mg/L Co etc. and LIX 622 in SX-1, up to about 97-98 % of copper present in the zinc sulphate leach solution was extracted with negligible co-extractions of zinc, iron, cadmium, cobalt, etc. pH modification was not required for this reagent. The copper loaded organic was almost completely stripped using 150 g/L sulphuric acid. Investigations into the effect of any possible organiclextractant contamination on zinc electrowinning showed (if any) little effect on current efficiency if the organic contamination is less than 45 ppm; current efficiencies of 95-97 % were obtained. At organic contaminations higher than 45 ppm, the current efficiency dropped to about 92- 94 %. Visually, the organic-contaminated cathode sheets had rough surface morphology, becoming more intense with increasing organic concentration, compared to the non-contaminated cathode sheets.

Jan 1, 1998

By Daojin Cao

The chemical components in the saturated aqueous solution of ammonium dimolybdate (ADM) were investigated at room temperature by comparative Raman spectroscopy. In order to explore the further detailed results, a new method of qualitative and half quantitative analyses, based on the main vibrant frequencies and the intensity ratio of the strongest peak to the second strongest peak recorded in Raman spectrum of saturated aqueous solution of ammonium heptamolybdate tetra hydrate (AHM), was put forward and attempted to analyze the chemical components of saturated aqueous solution of ADM. The results showed that there was obvious difference between Raman spectrum of saturated aqueous solution of ADM and that of ADM, but there were good relationships between Raman spectrum of saturated aqueous solution of ADM and Raman spectra of the three samples including AHM, the saturated aqueous solution of AHM and monomolybdate ion in aqueous solution. It was found that aggregated dimolybdate ion ({Mo2O72-}n)did not exist in the saturated aqueous solution, and was changed into heptamolybdate ion (Mo7O246-) and monomolybdate ion (MoO42-), which were in equilibrium each other, but the distribution ratio of heptamolybdate ion was larger than that of monomolybdate ion. In addition, Raman spectral pattern of saturated aqueous solution of ADM was reported.

Jan 1, 2006

By Malcolm J. Harrison

The problems associated with the flow control of abrasive slurries and solids laden fluids creates reliability problems in many mining operations. Conventional valves such as pinch, knife gate and plug types cannot always function reliably in such harsh operating environments. Due to the technological advances in the hard coating industry, ball valves can now be produced with internal surfaces protected from the erosive effects of these applications. Pressures well in excess of the capability of conventional 1000 kPa working pressure valves can now be handled reliably. The significant advantages of minimizing down-time and lowering maintenance costs can now be realized with metal seated ball valves.

Jan 1, 1999

By Toshiharu Hayashi

We prepared the water dispersed with Au particles ranging from 10 to 20 nm size by a novel wet chemical synthesis; generating seeds of Au cluster by adding a borane dimethylamine complex into chloroaureic acid (gold salt) solution, and then growing simultaneously with aminoalcohol included in the solution. As-prepared Au nano-particles with chemical surface modification were found to have some attractive performances, i.e., showing a high dispersiveness in an aqueous solution in a long time, sintering nano-particles at low temperature, and having low resistivity in the film prepared from nano-particles. In the case that smaller Au nano-particles were removed from as-prepared colloid, especially, Au thin film formed on the surface of Si plate showed the excellent value of 7.0x10-6ohm cm (reference peculiar resistance: 2.35x10-6 ohm cm).The sintering temperature was dependent on the elimination of 2-aminoethanol that modified on the surface of Au nano-particles.

Jan 1, 2006

By R. Upadhyaya

Aluminium alloy matrix cast composites have been synthesised by incorporating fine graphite powders (0.5 - 20 µm size) and chopped carbon fibres (6.5 pm P). 3-6 mm length) by liquid metallurgy technique. Incorporation of these second phase materials exceeding 6-8 wt% invariably resulted in agglomeration of the dispersoids and sometimes leading to even total rejection. It was found that small additions of mischmetal (1-3 wt%) during dispersion resulted in better incorporation without much agglomeration of the dispersoid as evident from the macro and micro structures of the composites. Further, the additions of mischmetal increased the volume of the effective incorporation of the dispersoid even to the extent 50- 60%. The mischmetal addition results in a significant increase in the power factor of the stirrer motor indicating an apparent increase in the viscosity of the system. The higher viscosity of the melt increase the shear transmission conditions within the melt during stirring thereby breaking the agglomerates of the dispersoids. The increased viscosity of the melt seems to be due to the formation rare earth - aluminium inter metallics precipitation, as observed in the metallographic studies, thereby making the process a "pseudorheocasting? technique. A provisional patent has been filed based on this work.

Jan 1, 1989

By P. Regan

Following the introduction of the Contilanod process over 10 years ago at Copper Range and IMI Refiners, significant changes and advances have been made to this pioneering anode production technique. A new radial flow metal feeding concept has been developed that allows a substantial increase in casting rates on the Hazelett® twin-belt caster. To cut the 45 mm thick continuous anode plate into shaped anodes at rates of 100 t/h or more, a filly moving hydraulic shear designed by Mannesmann Demag has replaced the slower speed plasma cutting torch. Details of the.new caster and shear are presented along with operating results from the new lines starting up in 1999 at the Gresik smelter/refinery in Indonesia and the completely revitalized Mansfelder Kupfer und Messing complex in Germany.

Jan 1, 1999

By Qin Li

An highly active absorbent with oxidization based on fly ash, lime and additives was prepared. Experiments of simultaneous desulphurization and denitrification were carried out using fixture bed and duct injection. The influential factors for the absorptive capacity of the absorbent were studied. The absorptive capacities of 120.7mg for SO2 and 43.7 mg for NOx were achieved at a Ca/(S + N) molar ratio 1.2, respectively, corresponding removal efficiencies of 87% and 76%, while spent absorbent appeared in the form of dry powder. The optimal temperature and humidity of flue gas treated with this process were shown to be approximately 50\\176 and 5% respectively. The mechanism of removal for SO2 and NOx was investigated. In comparison with traditional dry FGD, this process appears to have lower cost, less complicated configuration and simpler disposal of used absorbent. The valuable references can be provided for industrial application by this process. The foreground of application will be vast in China and in the world.

Jan 1, 2006

By Metehan Erdogan, Orhan Gökçe Göksu, Ishak Karakaya

"An experiment (mixture) design was created to optimize the process parameters of the electrochemical reduction of CaW04 to W in molten CaCl2-NaCl eutectic mixture. Temperature, applied voltage and the length of Kanthal wire winding of the CaW04 pellets were selected as the process parameters that were allowed to vary between the predetermined minimum and maximum values. The rates of the electrochemical reductions were interpreted from the variations of current and total charge vs. time graphs under different conditions. The analysis pointed out that 640°C and 2.81 V resulted in the fastest reduction. Itwas seen that the effect of Kanthal wire winding on the output current was less pronounced when compared to the other two parameters.IntroductionFFC Cambridge Process [1] has been applied to a number of metal oxides in laboratory experiments to produce metals. In nearly all of these studies, the electrolysis temperature was around 900°C, the electrolyte was pure CaCl2 or CaCl2 containing salt solutions and the anode was graphite. However, it was recently shown that the electrochemical reduction process of metal oxides in CaCl2 containing electrolytes at the mentioned high temperatures was not suitable for tungsten production [2], It was reported that as soon as WO3 contacts CaCl2, the following reaction occurs:"

Jan 1, 2012

By Alan M. Peel

"Over the past years there has been an increasing demand by aluminium cast -house operations to obtain a greater return from their existing installed plant. This has included increasing existing furnace production capacity to match new and higher downstream production requirements, reducing melt losses and more efficient alloying.The paper discusses how Electromagnetic Pumping, which was developed for the combined purpose of;1. Melting light gauge aluminium scrap with a reduced melt loss and; 2. Effective circulation of the aluminium melt,has established its self in recent years, as an effective means of satisfying many of these industry requirements, but how it has also provided many other additional operational benefits to the aluminium cast house.The paper will discuss operational performance of the system with a particular emphasis on its effect on the metal bath quality (alloying, chemical and temperature homogeneity), metal recovery and increased production due to the high circulation.The technology having now been adopted by a variety of industry leaders has a number of prominent references and the paper will discuss the operational benefits and experiences from some of these."

Jan 1, 2000

By M. A. Llavona

The study of the formation and components of copper patina and its conservation has assumed great importance. The changing environment has accelerated the processes of patinas degradation; thus, the exhaustive study of factors capable of affecting the patina formation, growth and durability has assumed great importance for the industrial activity of copper. The main components of the patina, oxides, chlorides, nitrates and sulfates, have been determined; the effect of physical, chemical and microbiological factors on patina formation, particularly the influence of acid rain, natural organic matter, particles and microorganisms have been defined. The effect of different electrolytic solutions that accelerate the formation of copper patinas has been determined, and a review of the state of knowledge of the formation and evolution of metal patinas has been made.

Jan 1, 1999

By Hiroyuki Matsuura

The effects of P20S or Na20 addition on the reaction rate of CO2 dissociation on the surface of FexO-base molten oxides was investigated at 1773K by isotope exchange methodl-6_ The rate constant decreased with increasing P20S content of molten oxides and the residual rate constant was observed at high P20S content On the other hand, the rate constant increased with increasing Na2O content for FexO-SiO2 melts. The rate constant was evaluated by the composition of oxides and the rate controlling step of CO2 dissociation was discussed.

Jan 1, 2003

By Seiji Yokoyama

As a series of fundamental study on the gas evaporation method, a levitation-melted aluminum was evaporated in the gas mixture of argon and ammonia to synthesize ultrafine particles of aluminum nitride. When the ammonia partial pressure were more than 2kPa, the formation ratio of aluminum nitride was about 95%. The particles of aluminum nitride were mainly hexagonal. The mean size of the particles of aluminum nitride was about 57 nm, and it was constant without depending on the temperature of the levitated aluminum and the partial pressure pf ammonia. The aluminum nitride was formed by the reaction between ammonia and condensed liquid aluminum particle whose size was relatively small.

Jan 1, 2006

By Hiroyuki Matsuura

The effects of P2OS or Na2O addition on the reaction rate of CO2 dissociation on the surface of FexO-base molten oxides was investigated at I 773K by isotope exchange method 1-6. The rate constant decreased with increasing P2Os content of molten oxides and the residual rate constant was observed at high P2OS content. On the other hand, the rate constant increased with increasing Na20 content for FexO-SiO2 melts, The rate constant was evaluated by the composition of oxides and the rate controlling step of CO2 dissociation was discussed.

Jan 1, 2003

By Leonard J. Friedman

The recovery of sulfur dioxide from metallurgical gases for the production of sulfuric acid has been an effective means of reducing sulfur dioxide emissions from non-ferrous smelters. Sulfuric acid has been produced from gas originating from fluid bed roasters, electric furnaces, reverberatory furnaces, flash smelting furnaces, Pierce Smith and flash converters, sinter machines, etc. The gas from each of these sources has a unique set of variables that affect the design and operation of the sulfuric acid plant. In addition, the sulfuric acid plant itself has been evolving, with new equipment designs and materials. This paper will review each of the unit operations in the gas cleaning and contact sections of the metallurgical sulfuric acid plant, discussing various equipment designs, materials and the handling of gas stream variables and impurities. The paper updates to 2006 previous works on metallurgical sulfuric acid plants by the authors.

Jan 1, 2006

By R. M. Luna-Sánchez

Electrochemical studies, particularly Evans? diagrams, have been employed in hydrometallurgy to simulate and explain the redox phenomena that take place at mineral and metal surfaces during operations such as leaching and cementation. However, despite their utility, in some cases, the combination of the cathodic and anodic branches, determined separately, does not reproduce the chemical environment present when both processes occur simultaneously on a specific surface. In the present paper, limitations of Evans? diagrams are analyzed through two examples: silver sulfide cyanidation and gold cementation on zinc. In both cases, the surface kinetics are sensitive to the local pH and cyanide levels. When the electrochemical oxidation of silver sulfide or the reduction of gold are performed in the absence of its corresponding redox reaction, the local pH obtained does not simulate the real situation and the combined reaction kinetics may be very different from those determined from the Evans? diagrams.

Jan 1, 2003

By J. Antonio Barrera-Godinez, S. E. James, J. Sun

The solvent extraction separation of iron from a zinc sulfate medium using DEHPA was investigated. After loading, the ferric ions were reduced in the organic phase using metallic zinc. The ferrous ions produced could be easily stripped into a sulfate solution with pH values in the range of 1.4 to 2.0. The small, laboratory scale pilot system used in this study allowed for continuous cycling of the organic and strip aqueous solutions. It was possible to establish and evaluate a series of steady state conditions under selected operating paiameters. The effects of processing parameters such as solution chemistry, flow rates, zinc metal loading and pH on iron recovery and efficiency were also evaluated. Under proper conditions, it was possible to remove about 5 g/L iron from the organic phase in one stage and to produce a concentrated iron sulfate strip solution containing ferrous ion concentrations in the range of 90 to 130 g/L. Preliminary feasibility tests were also made on electrowinning metallic iron from the strip solutions and crystallizing ferrous sulfate as a means of making a marketable iron product.

Jan 1, 2000

By Takashi Araki

In this work, we have elucidated the two-step oxidative reaction mechanism of 2,4,5-trichlorophenol by adsorbing oxygen atom for oxidative decomposition reaction of 2,4,5-trichlorophenol on oxide catalyst surface using ab initio molecular orbital calculation. In the first oxidation, total energies of reaction products have been shown extremely stabilized at all oxidation positions. This reaction occurs due to charge transfer from benzene ring to adsorbing oxygen atom. As a result, 1£ bonding of benzene ring are weakened. However, the benzene ring of 2,4,5-trichlorophenol does not perform cleavage reaction. In the second oxidation, the benzene ring of2,4,5-trichlorophenol can perform cleavage reaction, since the second oxidation obtains larger stabilized energies than the first oxidation.

Jan 1, 2003

By V. A. Bryukvin

It has been found that by superimposing symmetric alternating current over the process, the rate of nickel and cobalt leaching from metallized products with copper sulfate solutions increases by a factor of 1.5 to 2.0 and the apparent activation energy of the process investigated is reduced from 12 down to 6.6 kcal/mole. It appears especially attractive to use alternating current for anodic dissolution (oxidation) of metallic scrap of refractory metals and their alloys in ammonia electrolytes permits production of high-grade commercial products in the form of respective ammonium salts using a short and virtually reagent-free process flowsheet. Similar approaches can be applied also for electrochemical processing of nickel and copper scrap in sulfuric acid media with subsequent recovery of pure sulfate salts or electrolytic processing. Electrochemical technology for recycling of tungsten-cobalt (WC 15) and tungsten-rhenium (WR 20) alloys has been also investigated. In the former case, anodic oxidation of carbide alloy was carried out in nitric acid electrolyte with production of pure tungstic acid. The research conducted has indicated that the physicochemical effect of alternating current results in a lower activation energy of electrode reactions due to changes in the mechanisms of the electrode reactions themselves.

Jan 1, 2006