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By Roberto Giovanardi, Isabella Lancellotti, Luisa Barbieri, Ercole Soragni, Fernanda Andreola

"Recovery of precious metals (PMs) is a present topic, as they are used almost in every electronicelectric device. Gold is the second PM in order of consumption (following silver) and it is almost ubiquitary in electronics where it mainly finds application to produce bonding wires in integrated circuits and as a coating for contacts and connectors. Given this, discontinued electronic and, with a minor role, electric devices may represent a primary source of PMs as gold mines or jewelery wastes.At present the recovery of gold from such waste is generally accomplished by two strategies: by oxidative thermal treatment followed by metallurgical or chemical processes or by cyanide chemical etching; both techniques do not represent the optimum as the first one deserves a great amount of energy and non-combustible pollutant slag and fumes are produced, while the second procedure comports the use of a highly pollutant agent as cyanide.The aim of this work is the characterization of different electronics scraps to evaluate the gold concentration, and the selective recovery of this metal using enviromentally-friendly techniques. In particular, a new process was developed in order to overcome such environmental and efficiency issues. The process reaches the goal of detach the gold film from the substrate by selective leaching of the supporting metal.IntroductionThe treatment of waste from electrical and electronic equipments is a current topic as their role in modern life is increasing. The disposal of such waste represents both an environmental and an economical concern due to the vast amount of both precious and non precious metals.The use of precious metals (PM) in this field is of primary importance given PM’s unique properties, which give to each of them a specific and irreplaceable role. Silver is the most used, with a demand of over 5000 tonnes per year, mainly for switches and contacts in electric appliances. Gold is the second PM in order of consumption (over 250 tonnes per year and 8% of the total demand) and it is almost ubiquitous in electronics where it finds application to produce bonding wires in integrated circuits and as a coating for contacts and connectors. It is also used as solder in integrated circuits (in alloy with tin) or for wide coatings where it ensures protection against corrosion. Palladium, platinum, rhodium and iridium follow in order of consumption [1- 3]."

Jan 1, 2008

By Chris T. Vild

"ABSTRACT NOT AVAILABLEPRESENTATION SUMMARYIntroductionToday, light gauge aluminum scrap is melted in sidewell furnaces using natural gas reverberatory burners. The scrap is introduced into the sidewell adjacent to the combustion chamber through a submerged archway. Super-heated metal is then pumped into the sidewell where it aids in melting the scrap. From the sidewell, the flow is returned to the combustion chamber through a second submerged archway at some lower temperature. Normally, the burners are set at a designed high fire level and the scrap is introduced at a rate to attempt to mat.ch the burner input. A thermocouple in the bath is programmed to throttle back the burners to low fire if a high temperature limit is exceeded.Jn many cases the thermal efficiencies of these furnaces can be very low. With inadequate circulation, air and natural gas furnaces run at a dismal 18% thermal efficiency. If a circulation system· is added, the efficiency can jump to 28%. For a $100 million lb/yr recycling facility, and natural gas prices reaching $4.50 per million Btu, fuel cost at 18% efficiency can reach $1 million per year. A 10% increase in thermal efficiency saves $350,000 a year in fuel costs.With an increase in thermal efficiency, furnace utilization also increases. A 10% increase in thermal efficiency would result in a 20 million Btu furnace producing 12,000 lb/hr up from 8,000 lb/hr or 35 million lb more produced per year. This is a 33% increase in output.Most current furnace development has focused on burner technology using oxy-fuel, regenerative burners, etc. However, thermal efficiency is also largely effected by the molten metal circulation rate and how well the scrap is mixed into the superheated metal. Therefore, the flow dynamics should be optimized first, before installing of more thermal power.Jn an effort to understand the effect of these variables, a series of computer models were made and the critical factors studied with the goal of demonstrating an increase in thermal efficiency and production. Large-scale graphical representations of these models will be presented."

Jan 1, 2000

By S. Goto, S. Yamashita, K. Hata

"The average consumption of zinc dust for purification of zinc leaching solution is more than 25 kg per tonne of electrolytic zinc. Authors proposed to remove impurities in zinc leaching solution by electrolysis instead of cementation by zinc dust. The effects of copper and arsenic on electrodeposition of cobalt in zinc sulfate solution were examined fundamentally using a potentiostat. It is observed that cobalt is easily deposited on a cathode at potentials under -480mV with arsenic. Mesh cathodes of stainless steel and lead anodes were used in a small electrolytic cell and the electrolyte was circulated through 'the electrodes during the electrolysis. The effect of electrolyte circulating rate , pH, cell temperature, current density, and concentration of copper and arsenious ions on removal of cobalt were studied. Removal of Cd and Ni are also examined.IntroductionCobalt is difficult to remove from a zinc leaching solution by a simple cementation reaction using zinc dust. However, it is easily precipitated by zinc dust with co-addition of arsenious or stibinous oxide and copper ion in practical operations(I), (2), (3). The consumption of zinc dust for purification is 16-152 kg per tonne of electrolytic zinc and 65% of this zinc dust consumption is used for cobalt purification. The average retention time for purification of cobalt is 4.5 hours (1). A more economical process for purification is desired instead of zinc dust. The mechanism of this acceleration effect of copper and arsenious oxide on removal of cobalt are explained by the authorsas follows; a galvanic cell is formed between zinc dust and copper which is precipitated firstly, and cobalt is reduced on copper as Co-As alloy by this galvanic current(2). This assumption was confirmed in experiments using a galvanic cell with a membrane( 4). The following galvanic reactions occur between zinc dust and copper precipitate; on copper cathode,2H+ + 2e -= Hz(g)2Coz+ + 2HAs02 + 6H ++ 10e -= 2CoAs + 4HzOand on zinc anode,Zn = Zn = 2+ 2e –This galvanic current becomes almost zero in a zinc sulfate solution which includes only cobalt and no arsenious oxide, and cobalt is weakly deposited on a copper cathode. Cobalt deposition requiers a high degree of cathodic polarization. However, the galvanic current flows almost constantly in an electrolyte, which includes arsenious oxide, and the cathode potential is kept at about -500mV. Cobalt is precipitated as Co-As on the cathode.The authors assumed that cobalt may be removed by electrolysis at a very low current density instead of zinc dust and the following experiments were carried out. In the first part of this paper, the fundamental experiments using a potentiostat on the behaviour of cobalt in zinc sulfate solution are described. In the second part, the results of the electrolysis are reported. Cobalt is removed by a new type of an electrolytic cell, which was desigoed to <Iccelerate the rate of deposition of cobalt. The removal of cadmium and nickel in a solution which includes cobalt and arsenic are also examined."

Jan 1, 1997

By K. Prashant Sarswat

Isotopes are critical to a variety of applications including physical science analyses, biology, medicine, pharmaceuticals, and national security. In most cases isotopes must be relatively pure or highly enriched before they become useful. Current isotope separation technologies are relatively inefficient, capital and labor intensive, and often produced by a limited number of suppliers. In the category of isotopes, lithium is among other important candidates. Lithium is found naturally in two isotopes, 6Li which accounts for 7.5% of all lithium, and 7Li which makes up the balance of 92.5%. Each of these isotopes is important to the nuclear industry. 7Li is often used in the form of lithium hydroxide which is used to control pH in pressurized water reactors. The current supply of 7Li is based mostly outside of the United States, and its long-term supply is uncertain. Apart from supply issues, the use of mercury for 7Li separation is also a concern in commercial processing using the most common and efficient approach [1–3]. Hence, a reliable, environmentally friendly, and efficient technique is needed to produce 7Li. In this line of investigations, the authors used a two-compartment system and significant separation was achieved. In this piece of research, some preliminary results are presented including cell design and actual isotope ratio after enrichment. Applying an electro-potential across two electrodes can be used to drive electromigration of Li isotopes. The electromigration is in addition to normal diffusion. Note that 6Li diffuses faster and hence there will be a lowering of the 6Li concentration near the positively charged electrode and an enhancement in 6Li near the negative electrode during the separation process. Similarly, 7Li will be more prevalent near the positive electrode and less prevalent near the negative electrode during the initial separation stage [1].

By S. P. Mathew

The ISASMELT Lead Process is a continuous two stage process for the production of crude lead from concentrate. It is based on the use of a top entry submerged Sirosmelt lance to produce turbulent baths in which high intensity smelting or reduction reactions can occur. The process involves oxidizing the concentrates in the first stage to produce a high lead slag. This slag is tapped continuously and transferred down a launder to a second furnace where it is reduced with coal. Crude lead and discard slag are tapped continuously from this furnace through a single taphole and separated in a conventional forehearth. Process and engineering design work for a commercial scale Lead ISASKELT plant designed to produce 60000 tpa crude lead has been completed. This plant is planned to be operational in 1991.

Jan 1, 1990

By Jafar Safarian

Bauxite is the main raw material used for the production of alumina (Al2O3) through the well-known commercial Bayer process. This process has significant challenges such as limitation in using low-grade bauxites as they contain significant amounts of impurities such as Fe, Si, Ti. The Bayer process residue, which is known as red mud, is also a global environmental challenge due to huge amount of this low value residue production. An alternative sustainable process with high potential to solve these problems and produce valuable and consumable by-products is a pyrometallurgical-hydrometallurgical process in which the low-grade bauxite ore is treated through a smelting-reduction process, yielding iron alloys and a calcium-aluminate slag. Alumina is then produced from the slag by hydrometallurgical treatment. In the present work, the reduction of pellets produced from different bauxite ores by hydrogen is studied and it is shown that complete iron oxides reduction is possible. Further smelting and smelting-aluminothermic reduction of the reduced pellets show that iron and silicon ferroalloys can be produced, in addition to a proper slag for alumina extraction.

By Jean-Christophe Gebelin, Mark Jolly, Samantha Jones

"The de-waxing process in investment casting is truly a black art which is carried out in a black hole - the autoclave. The process involves exposing wax, coated by a porous ceramic shell, to steam at a pressure of 10 bar and a temperature of about 180°C. The processes which then occur are truly multi-media and multi-physics. Steam condenses in the porous ceramic, wax melts and flows, the shells expand and sometimes crack. Why the shells crack is one of the most difficult questions asked in the industry.Modelling and validating the de-waxing process is not simple. The IRC at the University of Birmingham is attempting to model this process using Physica+ a code developed in the UK. This paper will present the latest results in this attempt to model one of the casting industries most intractable problems.IntroductionThe de-waxing process using an autoclave involves the following physical phenomena:· Flow of the steam in the autoclave;· Heat transfer from the steam to the wax, possibly through the shell;· Melting and flow of the wax.At the same time, other phenomena may occur, such as the flow of the steam through the shell, the condensation of the steam on the shell surface and on the wax pattern surface, the flow of wax the through the shell, etc ...This shows how complex the de-waxing process is from a physical point of view. The main defect that appears during this process is the cracking of the shell. Previous modelling work carried out by Snow [1] has shown that it is possible to predict the stress in the shell, making numerous assumptions. In this paper, the modelling to predict the state of stress in the shell that is currently in development at the University of Birmingham is presented together with the presentation ofthe physical phenomena to model and the assumptions used. The parameters that are needed in such models will also be discussed, and some experimental work undertaken at the moment presented."

Jan 1, 2001

By Sepideh Abolghasem, Juan Pablo Casas Rodriguez, Juan Camilo Osorio

Predicting flow stress at high strain-rates is a desirable practice for material behavior characterization. Sub-grain size has shown a huge influence in cutting forces and the workpiece surface finish determination during orthogonal cutting process. Hence, a prediction of flow stress as a function of thermomechanical conditions and sub-grain size is of great important which is studied in this work for OFHC copper. The principal thermomechanical conditions being strain, strain-rate and the accompanying temperature rise are characterized in Plane Strain Machining (PSM) and the resulting microstructure, sub-grain size, is quantified. Material maximum flow stress (a constitutive model) as a function of thermomechanical conditions and sub-grain size is predicted considering a saturated state in microstructure using optimization algorithms for reaching the validated temperature rise based on modified Hahn’s model. Evaluated models suggest a major influence of strain-rate and dislocation in temperature rise estimation and flow stress prediction leading to consideration of mechanical failure phenomenon involved in machining-based manufacturing processes.

Mar 1, 2018

By Yingtao Zhang, Shaofeng Du, Yiming Rong, Wenjun Zhao, Gang Wang

"20Cr2Ni4A steel is a kind of high quality steel mainly used for manufacturing high-duty gears in the world. The high-duty gear with good performance must have wear and fatigue resistance properties. In order to get the good properties, the high-duty gear needs a high hardness gear surface and a good hardness gradient along the depth direction. In this paper, the samples were designed and a vacuum carbonitriding process was put forward to improve the surface hardness of parts for 20Cr2Ni4A. The process contained carbonitriding, quenching, cryogenics, and tempering process. The surface hardness and hardness gradient of carbonitrided samples were measured and the good microstructure was gained. The surface hardness is 67.SHRC and the case depth is 1.2mm.IntroductionSteels are widely used in industry, but the fatigue strength and the wear resistance of steel is much low. So the heat treatment process is put forward to improve the mechanical properties of steel. It can be improved by high-energy heat treatment methods for medium-carbon and highcarbon steel. Those methods will not alter the chemistry of the base metal [ 1].For low-carbon steels, carburizing and quenching should be used to improve the steels' mechanical properties, especially the surface properties. Compared with the carburizing, carbonitriding has more advantages, such as a short production cycle, low temperature and small deformation of parts. Carbonitriding is a modified form of gas carburizing, rather than a form of nitriding. The modification consists of introducing ammonia into the gas carburizing atmosphere to add nitrogen to the carburized case as it is being produced. Nascent nitrogen forms at the work surface by the dissociation of ammonia in the furnace atmosphere; the nitrogen diffuses into the steel simultaneously with carbon. Typically, carbonitriding is carried out at a lower temperature and for a shorter time than is gas carburizing, producing a shallower case than is usual in production carburizing [2]. As a material surface strengthening technology, carbonitriding has been widely used in the production [3]. And vacuum carbonitriding process is better than carbonitriding, because the vacuum carbonitriding temperature can be higher than carbonitriding without surface oxidation."

Jan 1, 2014

By Mahesh C. Jha

Molybdenum, a major refractory metal, is widely used as an alloying element in steels and superalloys to improve their corrosion resistance, physical properties and mechanical strength, particularly at elevated temperatures. The current worldwide production and consumption is estimated at about 130,000 tons contained molybdenum per year. Molybdenum occurs in nature as molybdenite mineral and is recovered by a flotation process as a primary concentrate at molybdenum mines and as a byproduct concentrate at copper mines. The concentrate is roasted to a technical-grade molybdic oxide (tech oxide) in multiple-hearth roasters. About 80 percent of the tech oxide is sold, as such or after conversion to ferromolybdenum, for addition to iron and steel. The remainder is further refined to pure oxide and molybdate chemicals that are used in the manufacture of catalysts, specialty chemicals, molybdenum metal and superalloys. This paper discusses the various steps in the extractive metallurgy of molybdenum, from flotation of sulfide concentrate to reduction of pure oxide to molybdenum metal.

Nov 26, 1999

By Hong Yong Sohn, Miguel Olivas-Martinez

"Different approaches are used for calculating the ‘energy requirement’ of a process. The determination of energy requirement becomes confusing for a process in which a fuel is also a reactant. The key issue is which heat of chemical reaction should be included in the ‘energy requirement’ value. We will use the example of ironmaking processes to illustrate the problem. The different approaches essentially boil down to the question: does one include the combustion heat of the reductant used in the reduction reaction or just the heat of the reduction reaction? Depending on the viewpoint, either approach can be accepted; it is a matter of convention. There is a need, however, to select a standard approach because the absolute value of ‘energy requirement’ of a process depends on the choice. The energy requirement of a novel flash ironmaking process will be compared with that of an average blast furnace operation.IntroductionDifferent approaches are used for performing energy balance calculations and perhaps more significantly in presenting the ‘energy requirement’ of a process. The question becomes more involved for a process in which one or more reactants are also used to generate the process heat by combustion. Often the key issue is which heat of chemical reaction to include in presenting the ‘energy requirement’ of the process.It is worthwhile to note at the outset that the difference in energy requirements between different processes for converting similar raw materials to the same desired product is largely unaffected by the choice of chemical reactions to be included. However, the absolute value presented as the ‘energy requirement’ of a process can be different by a large amount depending on the approach. We use the example of ironmaking processes to illustrate the problem. In these processes, as currently practiced or under development, carbon and/or hydrocarbons (including hydrogen) are used as the fuel as well as the reactant for reducing the iron oxide mineral.The different approaches in this case essentially boil down to the following question: does one include the combustion heat of the reductant used in the reduction reaction or treat the reductant portion as just a reactant? Depending on the viewpoint, either approach can be considered acceptable. It is a matter of convention. There is a need, however, to select a standard approach because the absolute value of ‘energy requirement’ of an ironmaking process (e.g., the currently dominant blast furnace process) depends on such a choice. It is particularly important to clearly state the specific approach used when the energy requirement of ironmaking is compared with those of other industrial processes such as petrochemicals production."

Jan 1, 2014

By D. Nozadze

A new method of isothermal electro-contact diffusion welding of layered composites under pressure is offered. The scheme is developed and laboratory installation is created on which preproduction models of the layered composite of steel and aluminum is produced. A new method of electro-contact hot deformation is proposed for realization of diffusion welding by pressure of stratified blanks providing high-temperature isothermal process. In this case a rolling process or composite pressing is meshed with simultaneous electric current transmission in deformation center. Considering that a resistance of transient layer far exceeds the resistances of composite components, the heat release takes place intensively just in this layer. As the surfaces are approached over a distance of inter-atomic forces, the energy of boundary atoms easily reaches the energy threshold of capture with a formation of qualitatively new metallic bond. Proposed method, providing isothermal process in deformation center, excludes a necessity of previous preparation and prevention of surfaces. In this case strength of layer connection may approximate or exceed strength limit of cladding layer.

Jan 1, 2006

By Józef Czernecki

The Polish copper concentrates are characterised by low content of sulphur and iron. At KGHM Polska Miedz S.A. two copper production technologies are in use. The shaft furnace process is used at the Legnica Copper Smelter and the Glogów I Copper Smelter. A single-stage direct to blister Outokumpu flash smelting process is used at the- Glogów II Copper Smelter. Melting copper concentrates in the shaft furnaces is carried out in a reducing atmosphere and the product obtained is a matte. Instead, a result of melting copper concentrates by an oxidising flash process blister copper of a quality similar to that of converter copper is obtained. The annual copper production at KGHM Polska Miedz S.A. exceeds 450,000 tons. Another important metal is silver produced from slimes from copper electrolysis (about 1000 t/y). Moreover, such metals as Pb, Ni, Se, As, Au and other precious metals, including Pt and Pd, are recovered from various semiproducts. This paper presents technological flow sheet of the copper production in plants using the shaft furnaces and in another plant in which a single-state flash process is applied. Characteristics of products, methods of their utilisation, main parameters of particular technological operations, and advantages and shortcomings of the solution applied are presented. There are also discussed: the natural environment protection as well as directions of the KGHM Polska Miedz S.A. plants modernisation.

Jan 1, 1999

By Antonio de Lucas, Juan Francisco Rodríguez, Ignacio Gracia, Mª Teresa García

"The amount of waste of Polystyrene (PS) foams is increasing in last years due to their use in insulation, protecting and, storing many different food products. Conventional methods of recycling such as crushing and shrinking by heated air or frictional heat have the disadvantages of molecular degradation, resulting in a reduction of the quality of the recycled polymer. Dissolution and shrinking with suitable solvents is one of the cheapest and more efficient ways of polystyrene recycling but in the process of the solvent recovery by distillation a certain degree of molecular degradation is produced. In this way, CO2 supercritical technology appears as an interesting alternative for the elimination of solvent. This work proposes a global process to polystyrene recycling in two steps: a polystyrene dissolution with a suitable “green” solvent followed by its elimination by supercritical tecnologhy. In order to develop a “green process” the constituents of essential oils, limonene, terpinene, cymene, and phellandrene, are selected as the most appropriated solvents. Introduction In the last years, disposal of the non-biodegradable plastic wastes has been recognized as a serious environmental problem. Recycling these wastes has great interest in order to prevent the environmental pollution and to preserve natural sources (1, 2, 3). Since the Polystyrene foams (PS) is one of the most used foam in isolation, protecting and food storage most of recycling work is concerned with this polyolefin (4). The two main alternatives for treating polymer wastes are energy recycling, where wastes are incinerated, and mechanical recycling (5). Environmental argumentations such as toxic emissions are building up a public resistance against incineration process (6). Mechanical recycling is a popular recovery path for manufacturers and is carried out on single-polymer waste streams. Any way, the market for recycled products can only be found if the quality is close to that of the original. Unfortunately the process of classification and further recovery of these wastes makes them often more expensive than virgin plastic (7, 8). Solvent extraction is one of the cheapest and more efficient ways for PS recycling. If it is done in house of waste producers the separation between plastics could be easy and effective and the transport costs would be eliminated."

Jan 1, 2008

By John Petersen

Heap bioleaching technology has become well established for the exploitation of copper sulfide ores. Still, in many operations the rate of copper extraction is rather slow, often taking two years or more to recover 80% of the copper. Chalcocite, the most common secondary copper sulfide, leaches by a two-stage mechanism. The first stage is rapid, whereas the second stage has a high activation energy and proceeds slowly at ambient temperatures. Nonetheless, this rate is still considerably faster than what is typically realized in a full-scale heap. A comprehensive column bioleaching study of a chalcocite ore has shown that the chalcocite columns are leached in a zone-wise fashion. The first zone corresponds to the first stage of chalcocite leaching, where all ferric produced by the bacteria is immediately consumed and all acid entering with the feed solution is consumed within a relatively narrow band. The second stage of chalcocite leaching proceeds much more slowly in the wake of the first stage, within a zone that grows gradually over the entire length of the column. The overall rate of leaching is thus determined by the rate of acid supply into the column rather than by mineral or bacterial kinetics, at least until the entire column is engaged in second-stage chalcocite leaching. In full scale heaps, there is evidence to suggest that solution distribution favours channelling between relatively large clusters of material which are exposed only to stagnant solution. Reagents have to migrate into such clusters by diffusion, which retards the delivery of acid dramatically. Thus, we believe that the rate of chalcocite oxidation in heaps is governed by sideways diffusion rather than downward migration. Column experimental results have been reproduced with a comprehensive heap-modelling tool. The model predicts that by simply changing the length of the average diffusion channel from column conditions (a few cm) to heap conditions (tens of cm), extraction times can change from weeks to years under otherwise identical conditions.

Jan 1, 2003

By Georgios Kolliopoulos

Water is a critical commodity of our generation and a key compound for the chemical and mining industries. Sustainable industrial development is directly associated with the ability to recover clean water from contaminated sources. Forward Osmosis (FO) is a low-energy footprint membrane process allowing the recovery of clean water from high salinity effluent streams. In FO, water is recovered spontaneously into a concentrated draw solution (CDS). Energy is required to separate the recovered water from the resulting dilute draw solution (DDS). In the current work, the fundamentals of the FO process and the most important aspects affecting its performance are discussed. An energy comparison of FO and conventional water recovery technologies is presented. Finally, the opportunities FO presents in the field of hydrometallurgy are analyzed.

By Henk Dijkman

Existing metallurgical operations can be optimized by implementing engineered bioreactor systems in the process configuration. For instance, metals can be recovered safely and economically from process and waste streams using biogenic sulfide. This paper focuses upon possible applications of high rate biotechnology in metallurgy and mining. Metal recovery from liquid streams (process bleed streams, leach water, waste streams), integrated removal of (fugitive) SO2, treatment of acid blowdown and other options will be described. Practical examples are given. A large-scale application of biotechnology at Pasminco&apos;s Budel Zink refinery is described. Here, acid plant blowdown is treated together with electrolyte magnesium bleed. Concentrated zinc sulfide (10 tpd) is produced biologically, eliminating the production of gypsum and closing the refinery sulfur cycle. Recovery of metals from solution at Kovehute Pribram in the Czech Republic is the second practical example. In this case, H2S is produced on-site for metal removal from an alkaline slag dump leachate. At the Caribou mine in New Brunswick, Canada, acid mine drainage is treated with biogenic sulfide. This plant is situated upstream of a lime neutralization plant. As a result, reusable ZnS is produced, the volume of the sludge (gypsum and hydroxides) from the lime plant is reduced by 50%, the sludge is free of heavy metals and the final effluent concentration of heavy metals is in the ppb range. In the second phase of this project, metals will be recovered from stored tailings, resulting in significant revenues.

Jan 1, 2002

By Mario H. Castro-Cedeno

"A design for a handheld MEMS chemical detector is proposed. The detector will be used to detect trace amounts of chemicals in air. It can detect drugs, toxic chemicals and/or explosives. The proposed detector will use ion mobility spectrometry (IMS), a technique that is well known for accuracy and has been used in the past in suitcase sized chemical detectors. The separation and detection of the chemicals occurs in the drift channel and the process was modeled using the finite element method and CoventorWare modeling software. A manufacturing process sequence for the drift channel is proposed and was demonstrated.IntroductionThe goal of this effort is to design, mode~ and prototype a MEMS chip that will be the key component in an ion mobility spectrometer (IMS). This technique uses and asymmetric potential to separate the various ion species in a stream of incoming air [1-4]. One advantage of IMS is its ability to separate chemical species from air at atmospheric pressure and temperature. This is a requirement for a simple to use handheld drug or chemical detector. IMS can be used to detect drugs, toxic chemicals and explosives and it is well known for accuracy in detecting very small amounts of chemicals. This chemical detection technique has been used in the past, but not in handheld detectors.One variant of IMS is the high-field asymmetric waveform ion mobility spectrometry or FAIMS [3]. The FAIMS process, shown in Figure l, works as follows: a gas sample is admitted into the instrument where gas molecules are ionized, typically by a weak radioactive isotope source, ultraviolet light source; and more recently through field emission. The ions move along the length of a channel while they are separated in the transverse direction by an asymmetric electrical potential. The potential, in the form of an asymmetric waveform, causes relative motion between the various chemical species. The species that hit the charged top and bottom plates are neutralized and only those ions that move along the center are detectable as charged chemical ions at the end of the channel."

Jan 1, 2004

By Zhongming Ren

"A new process of near net shape continuous casting of metal pipe has been put out. The specialty of the process is that no inner core is used. The principle of the process has been presented, and the effect of several factors on the thickness of the pipe has been investigated experimentally and numerically. It is shown that the temperature and the level of the molten metal, cooling intensity of the mold, and the velocity of casting influenced the thickness of the pipe apparently. In order to improve evenness of the thickness of the pipe, the mold was dedicatedly designed, and special methods were taken. By this process, a metallic material like ""bamboo"" was fabricated.IntroductionMetal pipe is a widely used material. Up to now, many processes have been put out to produce the pipe. However, the processes are usually expensive and inefficient. For instance, the welding pipe, which is most widely used, is produced through continuous casting of slab, rolling of the slab into sheet, and welding, with several times of heating and processing. Continuous casting of pipe can not produce small diameter of pipe, which is mostly needed, due to the inner core. Even though. OCC process is novel in fabricating the pipe with small diameter, it is inefficient. In this paper, the no-inner core continuous casting of pipe was proposed. With this process, pipe with small diameter can be produced efficiently. The influence of several parameters on the thickness and evenness of piper wall. With this process, a ""bamboolike"" pipe was fabricated.ExperimentThe experimental apparatus is shown in Fig. I. It is composed of mold, furnace, melt level adjuster, and dummy pipe. In the process, the level of the melt was adjusted at a proper position, then the mold along with the dummy pipe was inserted into the melt in a certain depth. The melt in the mold began solidifying, forming a solid shell. After that, the dummy pipe was pulled upward in a certain speed, drawing the solid shell out of the mold. Thus, a pipe was continuously cast."

Jan 1, 2000

By C. S. Ek

Tests have been performed to recover silver and lead from residues produced after a super-hot leaching in a zinc hydrometallurgical plant operating with jarosite precipitation. When this residue is leached in ammoniaammonium sulfate or in diethylenetriamine solutions, lead dissolution is not complete and its recovery from the aqueous solutions is either difficult, due to the operating conditions, either expensive due to the amount of added reagents. In both cases, silver is partly dissolved, partly left in a new residue still containing lead and baryum sulfates. The best treatment seems to include a selective flotation producing first a silver concentrate assaying about I % Ag, then a 50 % lead concentrate collecting the baryum salts, and a final quartz-gypsum tailing. Metal recoveries can reach 50 % and 80 %, respectively.

Jan 1, 1989