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By J. N. Kondo, M. Hara, T. Smida, N. Ooto, K. Domen

"A porous material composed of two-dimensional anionic sheets of a layered perovskite, KSrNb30 10, was studied as photocatalyst for the production of Hz in the presence of alcohol sacrificial donors. Colloidal single and multi-layered HSr2Nb30 10 sheets were formed by intercalating ietra(n-buthylammonium) cations into the interlayeres of H+-exchanged KSr2Nb30 10 (HSr2Nb30 10), and addition of HN03 solution to the colloidal suspension precipitated the porous materials in which HSrNb30 10 sh~ets rand~mly stuck together. Original HSr2Nb30 10 before exfoliation had a BET surface area of 1 m2 g-1, whereas the surface area of a porous material prepared under optimal conditions exceeded 100 m2 g-1. The porous HSr2Nb30 10 had considerably higher photocatalytic'activitie8 for oxidation of 1-propanol and 1-buthanol than HSr2Nb39io, indicating that in the porous materials many niobate sheets are available for decomposition of these large alcohols.IntroductionQuite a research effort has gone into the design and study of porous materials. Such materials with large surface areas would have applications in highly efficient adsorbents or catalytic reactions.We have been studying photocatalytic reaction by cation-exchangeable layered metal oxides, where alkali metal cations are intercalated into the interlayers of inorganic sheets.[1,2] There are several advantages to using layered compounds rather than bulk powders for photocatalysis. Layered compound is rich in variety, in addition, modifications of them are easily performed by exchanging alkali metal cations in the inter layers for H + or other metal cations. The most important advantage is that some layered compounds have considerably high photocatalytic activities than bulk catalysts because the electrons and holes generated in each thin inorganic sheet readily reach interlayer spaces as reaction sites at the illterlayer spaces. It should be very important for further improvements· of layered photocatalysts to utilize two-dimensional inorganic sheets effectively."

Jan 1, 2000

By P. Chris Pistorius

Calcium treatment of alumina inclusions, to convert the alumina to molten or partially molten calcium aluminates, is a well-established treatment for steel, to improve the castability of aluminium-killed steel. However, the role of magnesium in calcium-treated steel is not fully clear, nor is the origin of the several percent of magnesium oxide that is often present in calcium-treated inclusions. To study this, steel was sampled after calcium treatment at an industrial steel plant, and the inclusions identified by energy-dispersive X-ray microanalysis (EDX) on polished sections of the samples (analysing the samples in a scanning electron microscope). The predicted fraction liquid in the inclusion was estimated from the ternary alumina-magnesia-lime phase diagram. Inclusions with higher CaO contents generally had lower MgO contents, indicating that the calcium wire is not the origin of the magnesium in the inclusions; this was also confirmed by wet chemical analysis of the calcium wire. Instead, it appears that magnesium-alumina spinel inclusions form during extended ladle contact after aluminium killing and before calcium treatment. While such spinels have been stated to cause poor castability (clogging the submerged-entry nozzle), it is clear that calcium treatment successfully modifies the spinel inclusions to mixed alumina-lime-magnesia inclusions, where the magnesia content contributes substantially to liquefaction of the inclusions: for typical MgO contents of around 10%, the range of Ca:O ratios which yield liquid (or partially liquid) inclusions is extended substantially to lower Ca:O ratios.

Jan 1, 2006

By Gordon Holcomb, George R. St. Pierre, Robert A. Rapp

Carbon/Carbon composites offer promise as high-temperature structural materials. A primary limitation on their application is the need to provide protection against oxidation in hot oxidizing environments. Silicon carbide conversion coatings have been shown to provide extended protection at temperatures of 1600°C. SiC coated C/C components have been used in several aerospace applications. In the present paper, the preparation of carbon fibers and their treatment during subsequent processing into coated components are discussed with particular emphasis on the processing variables that can result in improved oxidation resistance. In particular, the influence of substrate inhibitors and selective sealants for cracks in coated C/C components are analysed.

Jan 1, 1988

By Shaolong Chen

Feeding dry sulfide concentrate into smelting furnaces enhances process performance and reduces the energy consumption and exhaust gas flow. Direct heated rotary dryers and flash dryers have being replaced by rotary steam dryers featured by very low wear rate of the pipe heating elements and long maintenance interval. Impact of the drying processes on the environment receives more and more attention as the emission legislation tightens. In this regard, environmental factors such as SO2, CO2, dust and gas flow among rotary dryers, flash dryers and steam dryers were compared. Selection of a rotary steam dryer for copper and nickel concentrate drying would be an ideal solution to reduce the pollution of exhaust gas, as drying is achieved by indirect contact to the steam at relatively low drying temperature and as the off-gas contains almost only water vapor and air. The emissions can be significantly reduced and only small and simple off-gas handling units are needed.

Jan 1, 2006

By Yang Tian-zu

Sodium pyroantimonate which is widely used as the clarifier in the glass industry and as the synergist in anti-flaming industry respectively has a production history of about 30 years in China. At present there is the production capacity of about 20,000 tons per year in China and China is chief producer of sodium pyroantimonate. In this work the production processes adopted by the producers of China, the operation conditions and the product qualities of sodium pyroantimonate prepared by different preparation methods have been summarized, and on the basis of comparing the advantages and disadvantages for each process the most advanced method - the air-oxidation method was introduced in detail. The production processes of sodium pyroantimonate mainly include the method of oxidation by sodium nitrate, the oxidation method of hydrogen peroxide, the potash salt method, the chlorination method and the air-oxidation method etc. The method of oxidation by sodium nitrate in which the crude antimony oxide, sodium carbonate and sodium nitrate are separately used as the raw material, the flux agent and the oxidant, has the advantage of short and simple technological process, but low grade quality of sodium pyroantimonate and bringing about serious environmental pollution are the disadvantages and this method has been substituted by other methods. Sodium pyroantimonate can be directly prepared by the hydrogen peroxide oxidation method with the advantages of simple technological process, high grade quality of the product and little environmental pollution. High grade quality of sodium pyroantimonate can be also synthesized by the potash salt method, in which industrial antimony white, the hydrogen peroxide, potassium hydroxide and sodium hydroxide are applied as the starting material. The disadvantages of these two preparation methods are high production cost and high requirements on the raw materials. The chlorination method with the crude antimony oxide, hydrochloric acid and chlorine as the raw material has the advantages of low production cost and high grade quality of the product. However complex process, high requirement of anti-corrosion for the equipments and producing plenty of waste water limit its application. The air-oxidation method with stibnite/jamesonite concentrate, sodium sulfide, and sodium hydroxide as the raw material and atmosphere as the oxidant is a newly developed method and its advantages are low production cost and the complex raw material can be treated by this method and its disadvantage is that the quality of sodium pyroantimonate is lower than that prepared by the oxidation method of hydrogen peroxide and the potash salt method.

Jan 1, 2006

By Thomas Brynjulfsen, Merete Tangstad

"Manganese ore fines, generated during mining and transportation, can not be added to the submerged arc furnace directly as they will prevent even gas flow through the burden. Low gas permeability in the burden will lower the degree of pre-reduction of ore and subsequently increase the carbon and energy consumption of the process. In order to utilize manganese ore fines in the furnace they are agglomerated into sinter, pellet or briquettes. The agglomeration process will however change the reduction properties of the ore. In this work the melting and reduction properties of sinter has been investigated.The melting temperature and melting mechanisms has been studied. The mineralogy of the raw ores and agglomerated has been found using XRD, and the composition established using EPMA(WDS). The effect of adding fluxes such as dolomite and quartz has also been investigated.IntroductionManganese metal is produced in a submerged electric arc furnace or in blast furnaces. The reduction of manganese oxide in blast furnace has in the recent years become more unusual due to the high consumption of reducing carbon material[5]. Manganese metal for alloying in steel usually contains silicon and iron, and are therefore called ferro manganese and silicomanganese.During mining, transportation and handling the manganese ore is broken up into different size fractions. The larger lump are used directly in the electric arc furnace, but the finer materials can not be added without treatment. The fine ore can disrupt the flow of CO and CO2 gas through the burden, subsequently reducing the degree of pre-reduction. The fine fractions must therefore be agglomerated into larger lumps, in order to promote gas flow. This can be achieved through a number of different processes. The agglomerate used in this work has been sintered, which means that is has been partly molten and reduced, in order to create bigger lumps."

Jan 1, 2012

By W. John Rankin

Professionals, technical and non-technical, working in the mineral and metal commodity industries need to understand the concept of sustainability and its implications for the industry. Undergraduate courses have not done this well in the past. Much has been written in this field, and there have been great advances in understanding. However, much of what has been published is superficial and sometimes misleading, and there is as yet no coherent, single account that can serve as an introduction or overview for mineral industry graduates. This paper presents an outline which can guide readers in developing an understanding of the topic and its relevance to their work. Key references are provided, particularly those accessible on the internet, which will serve to introduce the reader to the important principles and understandings. The guide should also be useful to academics preparing students to work in the minerals and metal production sectors.

Jan 1, 2010

By Ki Bui Ma

Momentum wheels with superconducting bearings can integrate both attitude control and energy storage functions, with attendant savings in the total volume and weight of hardware, and power consumption, all of which are in short supply on mini-satellites. We have built and tested a prototype with a wheel of mass 1.9 kg, diameter 3.25 in, and height 3 in, which can store 3.5 J-sec of angular momentum and 5 kJ of energy when it rotates at an angular speed of 15000 RPM. The energy density of 2.5 kJ/kg achieved is comparable with the lower range for lead-acid batteries. To show that the wheel is energy efficient, we have performed spin down tests and measured the input power required to sustain rotational speed. Results indicate that power consumption, even accounting for the needs of cooling system, is significantly smaller than that for state of the art commercial reaction wheels.

Jan 1, 2002

By V. A. Bryukvin

A hydroelectrochemical technology has been proposed and experimentally proven for processing metallic gold- and silver-containing concentrates on the basis of copper and copper alloys obtained as a result of preliminary physico-mechanical upgrading of electronic scrap. The proposed technology is based on hydroelectrochemical leaching of scrap using reversible electric current and diluted nitric acid solutions, containing complexing agents, permitting complete separation of gold from the nonferrous matrix without involving gold in the process, and dissolving copper, zinc, lead and tin virtually without any emission of nitrose gases.

Jan 1, 2006

By Jinqian Zhao, Jiarong Li, Shizhong Liu

"Creep cavitation of in single crystal (SX) superalloy was investigated. The constant load creep tests, in single crystal superalloys DD6, were conducted at the conditions of 800°C/700MPa, 850°C/550MPa and 900°C/450MPa, respectively. It was found that there were square facets on the stress fracture surface, and microscopic cavities in the ruptured specimens in the vicinity of the fracture surface. Both the square facets on the fracture surface and microscopic cavities in the section of the ruptured specimens show the morphology of the same thing at the different views, namely creep cavities, which are take the form of flatten cuboid. In fact, creep cavities are the longitudinally tensiled creep cracks slowly growing during the stress tensiling. The factors of creep cracks nucleation and growth conditions include: (a) enough high temperature to activate diffusion (b) casting pores as nucleation origination (c) high strains and strain rates. Eventually, the instantaneous fracture mechanism of creep specimen is cleavage fracture.IntroductionFor the materials used in elevated temperature service, creep behavior has to be accounted for. It is well recognized that creep rupture in polycrystalline materials at high temperature occurs principally by the nucleation and growth of microscopic cavities at grain boundaries, followed by microscopic cavities linkage to form micro- and eventually macro-intergranular cracks[l,2]. Without the usual grain boundaries, SX superalloys have superior capabilities at high temperatures to polycrystalline superalloys, and have become an established feature of gas turbine technology where they are commonly employed in the manufacture of high performance blades[3]. A considerable amount of work has been done over the past tens of years, and many models for nucleation and growth of creep cavities have been proposed, however, those are mainly for polycrystalline materials.In order to improve creep resistance that single crystal superalloys, in which grain boundaries are removed, have been developed. Because there don't exist grain boundaries in SX superalloy, the mechanism of nucleation and growth of creep cavities must be different from that in polycrystalline materials.Understanding the formation and characteristics of creep cavitation is crucial to model the lives of single crystal superalloys.M. Marchionni and L.G. Zhao et al. found that there were square facets on the stress fracture surface [4,5]. Roger C. Reed pointed out creep cavities lie in the necked region[6]. In this paper, the effects on the formation of creep cavities are discussed, as well as the morphology of creep cavities and fracture mechanism of SX superalloys."

Jan 1, 2013

By Bernd Kopacek

"Nowadays more and more consumers substitute their conventional TV-sets and computer monitors by LCD panels. In the near future huge amounts of LCDs will start coming back to recycling. As LCDs with hazardous mercury backlight lamps are used an appropriate recycling technology has to be implemented.IntroductionLiquid Crystal Displays (LCDs) are widely used in notebooks, organizers, mobile phones, pocket calculators, measuring and control instruments, electronic games, hand-held miniature TVs, audio-video equipment, large signboards, automotive displays and more and more also for PC monitors and TVs.According to a study from Stanford Resources (San Jose, California) the annual value of LCDproducts reached 35 billion EUR in 2002, about 30% of this within the European Union, representing a total area of 2,1 million m2 Liquid Crystal Displays. An annual increase rate of about 15% is estimated for the next years (up to 4,1 million m2 in 2005).As LCDs are already on the market for several years, larger quantities of the more than 2,5 billion LCDs are coming into their End-of-Life stage for treatment. In 2005 this figure will become even more dramatic - 40.000 tons of LCD-modules contained in 2 million tons of waste electrical and electronic equipment (WEEE) or about 30% of total WEEE within EU. An amount which is representing 400 million EUR costs for incineration.Currently the only method used to deal with redundant LCD units is incineration or landfill. Both are expensive and causes emissions into the atmosphere (global warming) respectively water contamination (Class II) and difficulties in biodegradation. Up to now there is no recycling solution for LC-Displays available.As a consequence European Commission requests the disassembly of LCDs with an area bigger than 100 cm2 in the Directive 2002/96/EC of the European Parliament and of the Council on Waste Electrical and Electronic Equipment (WEEE Directive) of February 13, 2003."

Jan 1, 2008

By G. Cifuentes

It is known that the cathode purity and the electrolyte treatment are affected by the solids present in the electrolyte. Anodic slimes properties (e.g., chemical composition, crystalline composition, sedimentation) were studied in copper electrorefining. These properties were modified through anodic composition and current density. In this investigation, we have worked with anode material from the Ventana Smelting, Hernan Videla Lira Smelting (ex - Paipote) of ENAMI (National Mining Company) and El Teniente Smelting of CODELCO-Chile (National Corporation of Copper of Chile). The characterization of the anodic slimes was done as a function of current density and anodic composition.

Jan 1, 1999

By P. G. Schirk, D. J. Roth

ALTEK has developed a processing system that can receive large pieces of dross & bath, of various metal contents, and reduce and separate these highly metallic concentrates into oxides and non-metallics. This system achieves these results without grinding the metallics into fines. Its unique feature results in the preservation of metallic unit in its largest possible size, which allows for maximum .metal recoveries. The Tumbler, an ALTEK-Didion International joint development, and the ALTEK High Velocity Impacting System (HVIS) are the key elements to this process. This paper will explore the advantage of this cold cleaning system over the direct melting of the raw dross in the reduction of landfill waste. The system also works well for removal of the aluminum from bath from primary smelters.

Jan 1, 2000

By David A. Army

Many times, the maintenance professionals have been involved in changes to processes or systems. Often they rely on seat of the pants knowledge to determine whether or not they were successful. More often than not, once our attention has been turned to other endeavors, the initiative has floundered. This paper will describe those measures that can be most effectively used to track and manage the success of implementing an improved Work Management System. However, not only will the paper discuss traditional work indicators, it will also explain how to establish the behaviors in the work place that will ultimately ensure successful implementation. Combined with the discussion on indicators will be a discussion on how to tie them to bottom line results and display them in the form of a scorecard. Actual results will be discussed.

Jan 1, 2006

By Pekka Parvinen, Saija Luukkanen, Pentti Pirkonen, Väinö Hintikka, Hannu Sekki

In the study was developed a new method for the treatment soils contaminated by polychlorinated dibenzodioxin and dibenzofuran. The method is based on attrition of soil so that the contaminants absorbed on the particle surfaces are liberated with the fine fraction formed in the attrition process. Same the attrition process produces active surface which can absorb the free contaminants. Before starting the remediation process must be decided the limit value under which the residual concentration must lie. Then in the laboratory is performed an experiment in the base of which is determined the grain size level; material under which much be removed together with the contaminant. In the real sample has been found that after the attrition the limit value 0.5 ng/g (I-TEQ) is obtained when the fine under 0.1mm fraction (20% of the original soils amount) is removed together with the contaminants 96% (original level 10 ng/g; 100%).

Jan 1, 2008

By Hector M. Henao

There is an increasing trend in the copper smelters to recycle electronic materials, which contain relatively high concentration of precious metals. As a consequence, the amount of precious metals lost in the slag phase is increasing. To determine the portion of the precious metals chemically dissolved and that associated with the mechanically trapped matte in the slag will be a key factor to improve the recovery of those metals. Thus, an experimental study was carried out to determine the distribution of precious metals (Au, Pt, Pd, Rh, Ru) between the equilibrated copper matte and iron-silicate slag phases. The experiments were made in a magnesia crucible at 1573 K and a fixed partial pressure of SO2 of 0.1 atm for the matte grades between 40 and 70 mass% of copper. It was found that the distribution ratios (defined as mass% X in slag/mass% X in matte, where X represents the precious metal) are around 10-2 for Ru, 10-3 for Au, Pt and Pd and 10-4 for Rh. The distribution ratios show a tendency to increase when the grade of matte is increased.

Jan 1, 2006

By Yang Cui

The partition ratios of lead and antimony between liquid copper and MgO saturated Cu2O-CaO-SiO2 flux and their removal rate by using CuCl-based flux were measured between 1423 K and 1573 K. For Cu2O-CaO-MgOsatd. system, the partition ratio of Pb was not affected by the CaO content at 1573 K, while that of Sb increased with increasing CaO content. The maximum value was 160 at the CaO content of 15.4 mass%. For Cu2O-CaO-SiO2-MgOsatd. system, two liquid phases of calcium silicate rich phase and Cu2O rich phase were observed at 1573 K. The partition ratios of Pb and Sb between calcium silicate phase and liquid copper depended on the (mass%CaO)/(mass%SiO2) ratio. When the (mass%CaO)/(mass%SiO2) ratio increased, the partition ratio of Pb decreased and that of Sb increased. For CuCl flux, the removal of Pb from liquid copper at 1473 K was possible, and a relatively low concentration could be reached. Moreover, most of lead as metal chloride vaporized from flux. For the removal of antimony from liquid copper at 1423 K, it was difficult by CuCl flux, and the removal ratio was approximately 20% for 75 minutes. However, the addition of CaO or Na2CO3 to CuCl flux was relatively effective to remove antimony, and the concentration of antimony reached a relatively low value after 15 minutes by using CuCl-CaO or CuCl-Na2CO3fluxes. Moreover, a small part of antimony as chloride vaporized from flux.

Jan 1, 2006

By Cameron Hams

Noranda's Process Reactor and Codelco's Teniente Converter are physically similar vessels, which leads to the commonly held misconception that the two processes are the .same. However, notable differences in chemistry, operating philosophy, and construction make them quite dissimilar. This paper compares and contrasts the Noranda Reactor and the Teniente Converter, and attempts to explain some of the apparent differences in behaviour and performance. The results of a worldwide survey of most operating Noranda Reactors and Teniente Converters, along with those processes that have ceased operation or are planning to be started-up in the future, are presented.

Jan 1, 1999

By T. T. Chen, J. E. Dutrizac

Noranda Inc., CEZinc presently employs a cement-stabilization (jarofix) process to stabilize its jarosite residues for direct disposal. In this process, Portland cement partly decomposes Na-jarosite to form Ca6Fe2(SC>4)3(OH)i2.nH20, ferric hydroxide and sodium sulphate which further reacts to form gypsum; approximately one-third of the Na-jarosite reacts in the current commercial product. The cured jarofix products also contain minor amounts of various Ca-Al-Fe silicate-sulphate-hydrate phases and traces of calcite. Together with gypsum and a Ca-Fe sulphate phase, these species bond the various particles together, imparting mechanical strength and reducing the permeability. Water-soluble Zn and Mg are stabilized in the Ca-Al-Fe silicate-sulphate-hydrate phases. The freshly cured products usually contain small amounts of moisture and traces of residual Portland cement, which provides additional alkalinity for the neutralization of any residual acid species. Jarofix products stored for more than six years in the laboratory, after curing, are usually dry and exhibit the same micro-textures as those of the freshly cured products. However, the stored products are depleted in the Ca6Fe2(S04)3(OH)i2.nH20 and Portland cement phases, and are enriched in gypsum and calcite which reflects the highly alkaline environment of the jarofix products. The aged products also have increased amounts of the Ca-Al-Fe silicate-sulphate-hydrate phases which have elevated Zn and Mg contents. This implies a further immobilization of residual water-soluble Zn and Mg during stora

Jan 1, 2000

By Christine Wenzl, Andreas Filzwieser, Stefan Konetschnik

"The METTOP-BRX-Technology is a novel manifold electrolyte inlet, which allows improved productivity and production in new and existing tankhouses by achieving higher current efficiency and cathode quality, as well as using current densities higher than 400 A/m2. Two installation examples are shown: Montanwerke Brixlegg AG, Brixlegg, Austria (upgrade of existing tankhouse) and Xiangguang Copper, Yanggu, China (new tank house). Montanwerke Brixlegg AG has been using the METTOP-BRX-Technology since 2005, and converted half of the whole tankhouse to METTOP-BRX in 2011 in order to use a current density of more than 400 A/m2. Xiangguang Copper started up their second tankhouse in May 2011. This tankhouse was constructed in the same way as the existing tankhouse, but was designed for 292,000 t/a cathode copper (existing tankhouse: 200,000 t/a) by using the METTOP-BRX-Technology. This production increase is a consequence of a much higher current density, namely 410 A/m2, compared to 280 A/m2 in the old tankhouse.IntroductionCopper electrorefining has been practised for more than hundred years, the last big change being the implementation of stainless steel cathodes in the 1980s [1], In 2005, the METTOP-BRXTechnology was first introduced. This technology was developed jointly by METTOP and Montanwerke Brixlegg, Austria, and allows improvements in productivity and production in new and existing tankhouses in an economic way. The METTOP-BRX-Technology is a novel manifold inlet that allows improved tankhouse productivity by increasing current density and/or current efficiency while maintaining or improving cathode quality [2]."

Jan 1, 2012