Search Documents

By J. Rajesh Kumar

The extraction equilibrium study of tetravalent platinum was carried out using tri-octyl/decyl amine (Alamine 336) and bis(2,4,4-trimethylpentyl) monothiophosphinic acid (Cyanex 302) in kerosene from hydrochloric acid media to investigate their extraction capacity, since they have different donor atoms, ?N? and ?S?. Their distribution equlibria were studied as a function of acid, extractant, diluents and temperature. The title metal shows the inverse behavior at higher acid concentrations. Extraction of tetravalent platinum increases with increase of extractant concentration. The plot of log D vs. log [Extractant], mol.L-1 is linear with slopes 1±0.3, indicating the association of one mole of extractant with the extracted metal species. Stripping of metal from the loaded organic (LO) with mineral acids and bases such as hydrochloric, sulphuric, nitric acids and ammonia, hydrogen peroxide, sodium hydroxide, thio- urea were studied. Regeneration and recycling capacity of Alamine 336/Cyanex 302 and extraction behavior of associated elements was also studied.

Jan 1, 2009

BHP Hartley Platinum operates an electric smelting furnace to treat Cu-Ni-PGM concentrate at its plant in Selous, Zimbabwe. The furnace, originally built by others, has experienced problems including severe refractory erosion of the sidewall. Hatch Associates has designed several important improvements to the furnace, including: ? water-cooled copper cooling elements in the slag zone ?air-cooled copper cooling fins at the metal level ?water-cooled copper tapholes ?binding system providing vertical refractory compression ?electrode seals ?new feed pipes Novel construction techniques employed on this project to reduce shutdown duration are discussed.

Jan 1, 1999

By P. A. Rusin

Many manganiferous silver deposits remain undeveloped because standard chemical extraction methods yield poor recoveries or are ' environmentally unacceptable. Biotreatment of such ore deposits in our laboratory resulted in manganese and silver recoveries of greater than 90%. Ore and sediment samples were collected from mining sites in Colorado and Arizona. Portions of samples were incubated in a semi-solid mineral salts medium amended with 20 mM glucose mid manganese dioxide (Mn medium). The cultures were incubated at 3(fC until manganese reduction was detected by a .color change fr:om .black to clear. Bacteria from these cultures were purified on Tryptic Soy Agar and individual isolates were retested for Mn reduction by an agar overlay method. Bacteria were identified according to Bergefs Manual ?of Systematic . Bacteriology. Most of the Mn-reducing bacteria are Bacillus species. Bacterial manganese reduction kinetic experiments were performed in 52 ml mineral salts broth supplemented with manganiferous silver ore instead of manganese dioiide. These cultures were incubated with agitation for 16 d. Aliquots were removed periodically and analyzed for solubilized manganese by atoniic absorption (AA). Cyanide (1,0 M) Vias added to the remaining ore-medium mixture for a 24 h bottle roll. The supernatant was analyzed for soluble silver by AA. Similar experiments were conducted on a larger scale using 15% pulp density. After bfotreatment of the ore, standard bottle rolls were performed. The pregnant solutions and the residues were analyzed for manganese and silver?using AA or fire assay as appropriate. In sterile. controls-which received no biotreatment, manganese and silver recoveries were 0.3% and 10% respectively; During biotreatment, total manganese solubilizatiori was as high as 99.8%. The reduced manganese could . be stripped from ?the growth medium using hydrometallurgical techniques. Silver recovery vaned from 70% to 92.5%. Microbial treatment of refractory mangairlferous ores can result in high recoveries of manganese and silver. Retention time varies depending upon the relative concentrations of manganese, silver, and other metals in the ore with only two days required in some cases, The biotreatment of ore is environmentally' acceptable while the use. of chemicals such as sulfur dioxide is less so.

Jan 1, 1991

By Esperidiana A. B. Moura, Mariana N. Sartori, Vijaya K. Rangari, Angel Visentim Ortiz, Francisco R. V. Diaz, Rene R. Oliveira

"This work presents the preparation and characterization of a nanocomposite based on Poly(butylene terephthalate) PBT and Brazilian smectitic clay (bentonite chocolate clay). Before being incorporated as clay nanoparticles in PBT resin, the clay was organically modified by the addition of a quaternary salt and sodium carbonate. PBT/Clay nanocomposite (96.3:3.70 wt %) was obtained by using a twin-screw extruder machine. After extrusion process, the nanocomposite was characterized by tensile, flexural and impact tests, SEM, Vicat, HDT, DSC, TGA and XRD tests. The results showed that the properties of the nanocomposite obtained were superior to those of neat PBT. Concerning the temperature of thermal distortion (HDT) an expressive gain of around 45 % was presented to PBT/Clay nanocomposite compared to PBT evidencing the interaction of nanofiller with the polymeric matrix.IntroductionPolymer-clay nanocomposites, also called as polymer layered silicates nanocomposites have attracted much attention from both industry and academia over the past decade because they frequently exhibit unexpected properties. In contrast to the traditional fillers, nanofillers, in particular, nanoclay, is found to be effective. The addition of a small amount (< 5 wt.%) can show significant improvement in mechanical, thermal and barrier properties, flammability resistance, and electrical/electronic properties of the final polymer nanocomposite without requiring special processing techniques. Also, as with other nano-size particles, the overall crystallization rate and the glass transition temperature are also affected. It is generally believed that the improvement of properties of nanoclay composites is directly related to the complete exfoliation of silicate layers in the polymer matrix. However, a processing technique that produces complete exfoliation is still a technical challenge [1,2]."

Jan 1, 2012

By Sunil Jayasekera

This paper describes the results of a study carried out to examine the feasibility of electrolytic recovery of silver from cyanide leach liquor generated from a Western Australian silver mine tailings using a novel high mass transfer electrowinning cell. The proposed circuit involves heap leaching and electrowinning in a closed loop. The filter-press-like closed electrode arrangement of the cell allowed much improved mass transfer of metal ions to the cathode surface, making direct electrowinning of metals from dilute solutions feasible. The tests were conducted both in the laboratory and at large scale using a prototype with ~1.0 m2 cathode area. The results showed that the recovery of silver from as low as 250 mg L-1tenor was feasible. The silver deposit produced with the prototype cell was non-adherent and powdery and could be readily removed from the closed cell. A system was developed so that silver powder was discharged continuously during the run.

Jan 1, 2003

By P. R. Taylor

Titanium carbide and titanium diboride powders have been successfully synthesized by direct treatment of ilmenite concentrates in a non-transferred arc thermal plasma reactor. Methane gas was used as the reducing agent and boron oxide was used as the boron source in these processes. Free energy minimization plots were used to predict the behavior of each system under different molar ratios and operating conditions. Products were characterized by XRD, SEM and chemical analytical techniques. The average size of the ceramic product is in the submicron range. Metallic iron apparently is finely deposited on the surface of the titanium carbide or titanium diboride particles. Minor impurities such as silica, manganese and zircon were converted to the carbide form.

Jan 1, 1995

By A. Cullaj

During a period of 15 years the metallurgical and chemical complex of Elbasan containing more than 15 principal plants, producing cast-iron, steel, coke, nickel carbonate, nickel, cobalt, chromium and other products, discharged into air, river water and soil an extensive amount of hazardous wastes containing high toxic substances. A monitoring study for the levels of heavy metals in soils nearby the former plant is carried out for the first time. Very high levels (total and extractable) of contaminants such as nickel, cobalt and chromium are found in samples taken from a relatively vast territory including the city of Elbasan, situated 8 kilometres far from the plant. The most polluted samples present a total content of 1211.8 ? 2949.6 mg/kg Ni, 97.0 ? 181.2 mg/kg Co and 1358.7 ? 4130 mg/kg Cr. These levels exceed several times the phytotoxic thresholds and present a potential hazard for the inhabitants. This study, as part of a bigger multinational project on solid decontamination, will also serve to the possible application of the new phytoremediation and phytoextraction technologies, being developed in parallel in this project.

Jan 1, 2006

By Masanori Abe, Yoshitaka Kitamoto, Kazuhiro Nishimura

"Ferrite plating is a chemical processing which utilizes Fe2+ - Fe3+ oxidation to synthesizing polycrystalline films of ferromagnetic spinels (MFe20 4, M = Fe, Co, Ni, Zn, Al, Cr, TI, etc:) directly from an aqueous solution at 24 - 100°C. This low temperature process allows us to fabricate new ferrite film devices on · substrates of such non-heat-resistant materials as plastics, GaAs integrated circuits, and biomaterials. Synthesized from an aqueous solution the ferrite plated ·films are highly biocompatible. Thus various magnetic device and biomedical applications have been proposed and realized using ferrite-plated films. Ferrite-encapsulated polymer microspheres are applied to antibody carries for enzyme immunoassay, and also to toners/carriers for photocopying. Perpendicular magnetic recording media utilizing plated CoNi ferrite films are proposed. The low-temperature synthesized films of NiZn and Co ferrites are potentially used as soft-magnetic and/or insulating layers, respectively at high/microwave frequencies.IntroductionFerrite plating is a processing which facilitates the formation of crystalline spinel ferrite films with various compositions, (Fe, M)30 4 (M = Fe, Co, Ni, Zn, Al, Cr, TI, etc.), directly from an aqueous solution at 60 - 100°C [1]. This opened the door to fabricating novel ferrite-film devices using substrates of such non-heat-resistant materials as plastics and GaAs integrated circuits [2-4]; conventional ferrite film preparation techniques such as sputtering, vacuum evaporation, MBE, LPE, etc., require high temperatures(> -600°C) for crystallization of ferrites, which deteriorates the non-heat-resistant substrates. Recently we extended ferrite plating to be preformed at room temperature [5, 6]. This enables us to use as substrates such organic materials as biomaterials (e.g. enzymes) having very low heat-resistance."

Jan 1, 2000

By Yong Zhao, Yan-hui Sun

Behaviors and evolutions of MgO·Al2O3 in non-oriented silicon steel during calcium treatment were investigated by thermodynamic calculations and high-temperature experiments. MgO·Al2O3 inclusions were the main type of inclusions before calcium treatment, which is also confirmed by the stability diagram of MgO/MgO·Al2O3/Al2O3 from thermodynamic calculations. After calcium treatment, the majority of original MgO·Al2O3 inclusions were mainly modified to CaO-MgO-Al2O3 system inclusions, this would be beneficial to improve castability and product quality of silicon steel. But there was no modification happening to some MgO·Al2O3 spinels which were directly surrounded by CaS inclusions. The content of Al2O3 occasionally existed a sudden increase besides a common decrease in the product layer of CaO·MgO·Al2O3. Then the evolution mechanisms of MgO·Al2O3 inclusions were proposed in present work. Thus, Al/Mg atom ratio had a significant influence on the modification of MgO·Al2O3 spinel.

Jan 1, 2016

By Jun Iwai, Osamu Takai, Yasushi Inoue, Hiroyuki Sugimura

"Infrared reflection absorption measurement was performed during plasma-enhanced chemical vapor deposition of silicon dioxide films at room temperature. Hydrocarbon contaminants adsorbed onto growing film surface are oxidized by oxygen radicals in plasma resulting functional groups which include C=O and C-O bondings. These groups exist only near the surface and are hydrolyzed rapidly after exposure to air.IntroductionRecently low-temperature silicon dioxide (SiO2) deposition has been in a growing industrial demand in pa1ticular, polymelic substrates such as polycarbonate and polyethylene telephthalate, which have poor heat resistance, need low process temperature (near room temperature) in coating of SiO2 which is a suitable material to improve optical and mechanical properties of polymenc products. Plasma enhanced chemical vapor deposition (PECVD) using organosilicon reactants is one of the most promising technique for lowering process temperature, so that it has been extensively studied1-12. In the present; however, hydrocarbon contaminants and a plenty of Si-OH termination in Si-O-Si networks tend to exist in the films, which degrade mechanical, optical and electrical properties of the films. It is necessary to understand the deposition mechanism at, low temperature in order to solve the problems. We have studied the low-temperature PECVD of Si02 by spectroscopic diagnosing techniques such as optical emission and mass analysis6-7, 11- 12Infrared reflection absorption spectroscopy (IR-RAS) has been a well-established technique for characterization of thin films on metals as· well as on semiconductors and insulators13-17. In this paper, we report on' the surface reaction of room-temperature PECVD of Si02by using in situ IR-RAS."

Jan 1, 2000

By Greg Dowling, Jun Ge, George Shannon, Shufeng Yang, Yongfeng Chen, Lifeng Zhang

"Inclusions in 316L stainless steel ingots poured using two different upgate designs – a traditional upgate and a swirl upgate - were investigated using SEM and ASPEX automated inclusion analysis. The main inclusions were high SiO2 inclusions, MnS inclusions and SiO2-Al2O3-CaO inclusions. More inclusions were detected at the top of the ingot than other places in vertical direction, and more inclusions were at the edge of the ingot than other place in the radial direction. With swirling upgate there were more K- and Na- bearing inclusions than that with the traditional upgate indicating possible more serious flux entrainment with the swirl upgate.IntroductionIngot casting still is very important for production of special steel grades including high carbon chromium bearing steel, thick plate, seamless tube, forgings, bars, and wire rods [1] . During the bottom teeming process, molten steel enters the trumpet and passes through the spider into the runners. Molten steel then enters the ingot mold through an upgate near the end of the runner. In the early stages of filling a mold, a mold flux bag hung in the mold were burnt and the mold flux will cover the top of the rising steel to protect the steel from being reoxidized, acting as well as act as a thermal insulator. So far, some efforts on studying inclusions characteristics in the ingot have been reported. A review paper on the control of inclusions during steel ingot casting was published by Zhang et al. [2] Zhang also studied Inclusions in bottom-teemed ingots of plain carbon steel and found that the >20µm inclusions originated from either the entrainment of mold flux of the reoxidation during teeming process. [3] The results of Nagendra and Du showed that there were more inclusions in the centre part of the ingot [4]. Eriksson et al reported that the composition of inclusions was more complex in the mold samples in comparison to the ladle samples, and more inclusions in the mold were found than in ladle because of the reaction between the mold flux and the molten steel [5]. It was reported that SiO2-CaO-Al2O3 inclusions originating from mold powder with reoxidation product Al2O3 as a part, and there were more inclusions close to the side wall than the center of the ingot in the radial direction. [6]. A more recent investigation showed that four main types of inclusions in runner samples were classified: oxides, sulfides, complex and carbon-nitrides. [7] The flow pattern in the mold during filling has been found to be an important factor regarding inclusions in the ingot. In the early stages offilling a mold, steel enters the mold through the entry nozzle at a high velocity. The effect of the resulting turbulence on the meniscus can lead to the entrainment of mold flux. Efforts have been paid over the years to find methods to reduce the velocity of the molten steel entering the mold, such as using opening angle of the inlet nozzle [8], using swirl blade at the runner [9], using a divergent nozzle combined with a swirling flow generated in the nozzle [10-11]."

Jan 1, 2012

By Wenjun Duan, Kun Wang, Qingbo Yu, Qin Qin

"A novel oxygen production technology noted chemical looping air separation (CLAS) was introduced and properties of Cu-based oxygen carriers used were investigated. The oxygen carriers were prepared by mechanical mixing. Al2O3, Fe2O3, ZrO2, TiO2 and SiO2 were used as binders during the preparation. XRD patterns show that spine! oxides are formed using Al2O3 and Fe2O3 as binders. Phases of CuO and binders keep stable using ZrO2, TiO2 and SiO2 as binders. BET values of oxygen carriers increase in the order of ZrO2>TiO2>SiO2>Fe2O3>Al2O3. The effects of temperatures, binders, particle sizes and flow rates on reduction/oxidation reaction rates were studied in TG experiments. The reduction reaction rate increases in the order of ZrO2>TiO2>SiO2. The effect of binders on the reactivity of oxidation is not obvious. The reduction and oxidation reaction rates both have the tendencies of increasing with the temperature increasing and with gas flow decreasing. However, the effects of gas flow and particle size are little.IntroductionChemical looping air separation (CLAS) is a novel oxygen production technology. The oxygen carriers used in CLAS release oxygen in reduction reactor and regenerate in the oxidation reactor. Selecting suitable oxygen carriers is the key for CLAS. Oxides of CuO, Mn2O3, Co3O4, Pb3O4, CrO2, SrO2, PdO2 and CeO2 have the property of releasing oxygen at suitable temperature and oxygen partial pressure [1]. Among these oxides, CuO, Mn2O3, Co3O4 are the most common compositions used to prepared oxygen carriers for chemical looping combustion (CLC) or chemical looping with oxygen uncoupling (CLOU) [2-5]. Moreover, thermodynamic calculations and preliminary experiments were carried out on oxides of Cu (CuO/Cu2O), Mn (Mn2O3/Mn3O4) and Co (Co3OJCoO) by Moghtaderi to ascertain their feasibility for CLAS process [6]. CuO has the highest oxygen transport capacity (0.1 g 02/g CuO compared to 0.03 g 02/g Mn2O3 and 0.06 g 02/g Co3O4). However, agglomeration is the biggest issue for copper oxides used at high temperature because of its low melting point (l 450°C for CuO, 1235°C for Cu2O and 1075°C for the mixture of CuO and Cu2O) [7]. In order to improve the capability of anti-sintering and stability ofCuO, binders (ZrO2, MgAl2O4, TiO2, SiO2, Fe2O3, Al2O3, cement) are added during the preparation of Cu-based oxygen carriers [8]. In this paper, the Cu-based oxygen carriers were prepared by mechanical mixing method. TiO2, Al2O3, Fe2O3, ZrO2 and SiO2 were selected as binder. XRD, BET and SEM were used to analyze the phase, surface area and surface morphology of oxygen carrier prepared. The reactivity of oxygen reduction and oxidation of oxygen carriers prepared were investigated in STA409PC thermal analyzer."

Jan 1, 2014

By William K. Tolley

The U.S. Bureau of Mines (USBM) is investigating hydrometallurgical processing techniques to recycle metals from semiconductors and other advanced materials. Cadmium and tellurium were recovered from mixed CdTe/CdS scrap produced in the manufacture of thin-film photovoltaic devices. Cadmium and tellurium dissolution was achieved using hydrogen peroxide in dilute sulfuric acid. Leaching the scrap in 2.2 N H2SO4 yielded 99% Cd extraction and 98% Te extraction. Sulfur remained in the leach residue primarily in the elemental form. Elemental tellurium was precipitated from the leach liquor by adding Na2S2O5. Cadmium sulfate was recovered by evaporation. A preliminary process evaluation suggests that the process may have economic potential. Alternative recovery schemes are discussed.

Jan 1, 1995

By Roma T. Dec

Many industrial wastes may require preliminary processing to change their particle size, density, surface properties or flowability to become more suitable for treatment and recycle. This can be achieved by pressure agglomeration using roll presses. In the following paper an overview of various roll press processing methods like briquetting, compacting, compacting-granulating or densification is presented together with basics of process and equipment design. The emphasis is focused on major factors influencing compaction process and responsible for pressure build up and final product quality. Finally, two examples of roll press application for briquetting of steel plant wastes and compaction of alumina base catalyst tailings are introduced.

Jan 1, 1996

By Kazuki Morita

Dissolution mechanism and solubility of chlorine in the oxide melts, such as CaO-SiO2-Al2O3 (-Na2O), Na2O-SiO2-Al2O3 and CaO-SiO2-FeO systems, have been equilibrium technique was employed with controlled Po2 and PCl2, (Po2 = 10-6 -10 19 atm, PCl2 10-6 -10-13 atm at 1673-1748 K). The solubility of chlorine in the 40mass%CaO-40mass%SiO2- 20mass%Al2O3, slag was found to vary in proportion to Pb2/ w and pc/z/p&apos; which proved that chlorine dissolved in the melts as C1 anion. Hence, the chloride capacity (CCI-), indicating the ability of molten oxide to absorb chlorine, has been defined as; The Ccl value was observed to increase with increasing slag basicity and temperature, and showed a reasonable relationship with that Of CS2-. Based on the result obtained in the present study, chlorine distribution during incineration with slags was predicted quantitatively.

Jan 1, 2003

By Chengxian Lui

Detailed mineralogical and metallurgical investigations were carried out on a phosphorous-bearing manganese carbonate ore from the Huayuan manganese mine, Hunan, China. Microprobe analyses indicate that the Manganese occurs mainly in calc-rhodochrosite and in rhodochrosite. The cOll&apos;pOsitional range of these manganese carbonate minerals is 50 -80 % MnOJ3, 0 -35 % CaOJ3, 5-35 % MgC03 and 0 -15 F~. The manganese carbonate minerals are very fine grained, IOOSt are between 4.6 and 9.4 1m in diameter. The small grains are clustered into aggregates that form bands 0.5 to 10 rnn wide. The phosphorous-bearing mineral in the ore is fluorapatite and is in grains that are generally smaller than 6 1m in diameter. Metallurgical tests show that it is possible to concentrate the aggregates of manganese carbonate minerals by high intensity magnetic separation, and to reduce the phosphorous content by rpasting the concentrate to convert the manganese carl::x>nates to insoluble hausmannite, and then leaching the roast product with HCI to dissolve the fluorapatite.

Jan 1, 1989

By F. Ajersch, P: Tsantrizos, K: Shanker

"TiN films have been deposited on various substrates by a novel reactive plasma technology. In this process, a nitrogen source (NH3 or N2) and TiCl4 are reacted in the jet of a plasma torch, and are deposited onto a substrate forming TiN films at a high growth rate ( > 2µm/min). It was found that the process parameters strongly affect the microstructure, thickness, density, and growth rate of the TiN films. These parameters include source of nitrogen (NH3 or N2, N/Ti ratio, temperature of substrate, and spray distance. In general, it was found that thick and dense coatings were deposited when the N:Ti ratio was kept low, and the substrate temperature was high. Also, for the series of conditions investigated, NH3 was found to give much better results than N2•. The limitations and advantages of this technique are also discussed in this paper.IntroductionTiN is an extremely hard material and is used in many wear applications, particularly as a protective coating on cutting tools to extend their Iife(1.2). Owing to its excellent chemical stability, TiN is also frequently used as a diffusion barrier in the electronics industry for sub-micron Al/TiN/Si ohmic contact systems (3) or as a coating on high-temperature resistant alloys in gas turbine applications (4), based on its good resistance to oxidation. Other applications include decorative coatings in the jewelry industry, and specialized applications such as solar energy absorbers and transparent heat mirrors(5).TiN films can be deposited/formed using various techniques. The main techniques of deposition are CVD (Chemical Vapour Deposition) and PVD (Physical Vapour Deposition). Each of these techniques can have many variations in equipment characteristics, reactants as well as a range of process parameters (pressure and temperature). In the CVD process, TiN is generally deposited onto a heated substrate where a chemical reaction takes place. The reaction can be one of reduction(6) (e.g.: TiCI4 + 0.5N2 + 2H2 --> TiN + 4HCI), of thermal decomposition(7) (e.g. decomposition of titanium dialkylamide), or of displacement (e.g. TiCI4 + NH3 --> TiN + 3HCI + 0.5CI2)' The displacement and reduction reactions are the most common."

Jan 1, 1994

By Fabio J. Esper, Guillermo R. Martín-Cortés, Francisco R. Valenzuela-Díaz, Cassio P. Carvalho, Giorgio Grotti, Reginaldo B. Santos

"Rejected sands from smelting metallurgical process because contain lead and others heavy metals are a problem to dispose as waste in all the countries. A procedure that is being proposed for it is to incorporate it on common clay bodies in the fabrication of structural ceramic products as bricks, blocks and roof tiles. The main goal of this paper is to present the results obtained with mixtures of sands from smelting metallurgical process with common clay from Jundiaí, São Paulo, Brazil. Preliminary incorporation tests (1,0% in weight) were made with hand formed spherical samples. With the higher compression strength of the spheres after drying and firing (950ºC) experiments on bricks production were made for quality technological test. Seven hundred hallow blocks containing 1,0% waste were produced and presented ceramic properties similar to those without sand incorporation. Introduction In last the fifteen years the LMPSol - Raw Materials & Non-metallic Solids Laboratory – Metallurgic Eng. & Materials Depto. – Polytechnic School - University of São Paulo comes studying the possibilities of incorporate industrials waste materials to the production of bricks and other products of construction aiming at to remove pollution products of the environments and to user the properties of the same ones in the structural ceramics products. Examples are the study of the influence of rejected steel furnace dusts in structural ceramic [1], another example is the main subject of the present paper: use of rejected sand from smelting metallurgical process in the production of bricks an other products of structural ceramics. Antecedents More or less one year ago, specialist and members from the direction board of METALÚRGICA GROFE LTD. Company contacted researchers and professors of the LMPSol – PMT – EPUSP seeking for a solution to their concern with the disposal of rejected sand from smelting metallurgical process."

Jan 1, 2008

By Denise Corrêa de Oliveira

Common dry batteries use zinc as the negative electrode. Producers commonly use additives such as mercury to prevent corrosion and to increase the mechanical resistance of the zinc anode. Alkaline batteries also contain it, as an anti-corrosive agent. When mixed with the common municipal solid waste, heavy metals as zinc and mercury pollute soil and ground water supplies, moving to the food-chain and affecting human health. Due to these possible damages, this kind of waste must be properly disposed, or recycled. Thus, even in low amounts (ppm) in batteries, mercury has to be eliminated or, at least, its content should be reduced. This work presents the use of pyromettalurgical processes, to reduce mercury content and recover zinc. The tests involved batteries treatment at temperatures from 300° to 1000°C. Mercury is eliminated up to 650°C, and zinc is evaporated at higher temperature treatment. C

Jan 1, 2001

By C. M. Wai

"Metal species in solid and liquid materials can be extracted by supercritical carbon dioxide containing a suitable ligand. This in situ che1ation-supercritical fluid extraction technique offers several advantages over conventional solvent extraction including minimization of organic liquid waste generation and exposure of personnel to organic vapors. One unique feature of this technique is that metal species can be removed from solid materials directly using supercritical carbon dioxide as a solvent. Several ligand systems including dithiocarbamates, B-diketones, organophosphorus reagents, and macrocyclic compounds have been tested for metal extraction in supercritical carbon dioxide. This novel extraction technique may have important applications for metal recovery and mineral processing.IntroductionSupercritical fluid extraction (SFE) offers several advantages over conventional solvent extraction including the minimization of organic liquid waste generation and exposure of personnel to organic vapors.[1] The high diffusivity, low viscosity, and T-P dependence of solvent strength are some attractive properties which make supercritical fluids excellent candidates for extraction and recovery of organic compounds from solid materials [2] Carbon dioxide is a gas of choice for SFE because of its moderate critical constants (Tc = 31 °·C and Pc = 73 atm), inertness, and availability in purified form. After extraction, the fluid phase is depressurized to separate organic solutes from CO2 gas and the gas can be recycled for repeated use. The SFE technology has been applied to industrial scale operations such as the preparation of decaffeinated coffee and hop extracts."

Jan 1, 1996