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By P. L. Sibrell

The U.S. Bureau of Mines has tested cyanide leaching for recovery of palladium (Pd) from spent petroleum processing catalysts. Three different catalyst samples were supplied by a spent-catalyst processor. These catalysts consisted of a zeolite base and contained 0.4 to 0.7 pct Pd. During alkaline cyanide leaching, the catalysts exhibited ion-exchange properties due to their zeolite matrices. Hydrogen ions were released from the zeolite in exchange for sodium ions in solution, resulting in a significant decrease in solution pH. This could present a safety hazard because of the potential for release of toxic hydrogen cyanide gas. A pretreatment .step where the catalysts were contacted with a 1.0M sodium hydroxide solution was found to prevent the pH shift from occurring. Following the sodium hydroxide pretreatment, two stages of leaching at 160 °C with solution containing 1 pct sodium cyanide and 0.1M sodium hydroxide gave at least 75 and up to 95 pct Pd recovery. The Pd was quantitatively recovered from the leach solution by thermal decomposition in an autoclave at 250 °C for 1 h. The Pd content of the precipitate was over 50 pct. Thermal decomposition also decreased the total cyanide content of the barren solution to less than 0.2 mg/L. The catalyst leach residues passed the Federal Toxicity Characteristic Leaching Procedure and the California Waste Extraction Test, indicating that landfill disposal of the leach residues would be acceptable.

Jan 1, 1995

By Jack Thibodeau

During the past six years, most states have promulgated water quality regulations which contain numerical aquatic life standards for heavy metals. In addition, the Environmental Protection Agency (EPA) promulgated national water quality standards in 1992 which also include numerical aquatic life criteria for heavy metals. Numerous wastewater discharge permits have been issued by the states and EPA to industrial facilities which include low microgram per liter heavy metal limitations. In many instances, the limitations are below detection limits or treatability limits using state-of-the-art analytical methods or treatment technologies. This paper will discuss options for conducting studies, including the use of water-effect ratios, metal partitioning coefficients, and recalculation procedures to develop site-specific metals criteria and higher permit limitations. The installation of expensive metal treatment systems to remove trace metals may be avoided if higher permit limits are indicated by the site-specific studies.

Jan 1, 1996

By Gunnar Eriksson

Computer simulation has become an everyday practice in thennodynamic and materials research. Advanced thennochemical algorithms take into account heat transfer effects and salient reaction kinetics when applied for process models. In particular, the combination of mass transfer or overall reaction rates with multi-component Gibbs energy minimisation provides an effective tool for simulation of industrial thennochemical processes and processing of materials. In this work the combination of rate factors with the Gibbs energy technique was studied by using the novel program ChemSheet, which operates through Microsoft's Excel® spreadsheets. Such processes as, for example, CVD of pure silicon production, titania pigment manufacturing, vapour pressure of Mercury in amalgams (in Hg-Iamp manufacturing) and melting behaviour of low-temperature alloys have been modelled. Provided that the thennochemical data is available simulations can be performed with any thennodynamic system. The calculation can be performed as an affinity study without a particular reactor model or with a specific reactor scheme.

Jan 1, 2001

By X. Jay Gao

A fast high-temperature carburizing process integrated with materials design and optimization via a systems design approach was developed to significantly reduce process cycle time. Process experiments were focused on boost cycles to obtain a robust boost process and investigate surface reaction kinetics, primary carbide formation and dissolution. Weight gain and microhardness were measured, all showing evidence of non-monotonic time evolution for longer boost times at higher temperatures. Optical and electron microscopy and other techniques have been used to identify possible carbides, their location and types. These results assist the picking of first boost time with least variation rate in terms of content of case carbon and carbides, dissolvable in subsequent diffuse if any. The results also provide critical information to properly formulate surface reaction kinetics and diffusion and formation kinetics of carbides modeled using DICTRA. Keywords: high temperature vacuum carburizing, partial pressure carburizing, heat treatment, process development, carbide, case hardening, microstructural analysis, over carburizing

Jan 1, 2003

By James D. Navratil

The mineral magnetite, or synthetically prepared iron ferrite (FeO?Fe2O3), has been used to separate a wide variety of substances, such as dissolved metal species and particulate matter, from wastewater. In the absence of an external magnetic field, activated magnetite readily adsorbs numerous metal species including actinide elements. In the presence of the external magnetic field, enhanced capacity was observed in using supported magnetite for removal of actinides and heavy metals from wastewater. The enhanced capacity is primarily due to magnetic filtration of colloidal and submicron particles along with some complex and ion exchange sorption mechanisms. The removal of the magnetic field and use of a regenerating solution can easily regenerate the loaded magnetite. The process has recently been tested for the removal of other metal ions including cobalt and iron. This paper will review previous work on the use of iron oxides for wastewater treatment and discuss the development and potential of the magnetic filtration/sorption process for wastewater treatment applications in hydrometallurgy.

Jan 1, 2003

By K. Takahashi, G. Dodbiba, T. Fujita, N. Sato, S. Matsuo, K. Okaya

Different materials are used for manufacturing various parts of a cellular phone. Considering that a great number of mobile phones are being discarded every year, it is important to recover these materials and then recycle them in order to save resources. The primary objective of this work is therefore to find and suggest ways on how to recover various materials from discarded cellular phones for recycling. Much effort, for example, has been put in recovering and recycling tin oxide (ITO), a mixture of indium (III) oxide, (UI2O3) and tin(IV) oxide from the discarded liquid crystal displays (LCDs). Here we report a simple and cost-effective process, which includes a HC1 treatment process for altering the structure of the indium (III) compound into a chlorideinduced indium compound, in order to facilitate the vaporization of indium at a relatively low temperature. The experimental results indicated that 96.2 % of indium can be recovered from ITO, when the sample was heated at 973 K for 90 minutes. In addition, some thermodynamic calculations were also carried out in order to better understand the mechanism for chlorideinduced vaporization of indium.

Jan 1, 2011

By David E. Jones

In any manufacturing process, the generation of secondary, associated or waste products along with the primary product is inevitable. Today there is great emphasis on the concept of waste minimisation. As part of that overall strategy, the search .for markets for these materials formally regarded as wastes, can mean the development of whole new industries. This paper examines some of the work necessary to develop recycling and markets for associated products with particular reference to iron and steelmaking slags.

Jan 1, 1994

By Hiroaki Kawamura, Takeshi Yoshikawa, Kazuki Morita, Yutaka Yanaba

"To develop an alternative metallurgical process for phosphorus removal in the production of solar-grade silicon (SOG-Si), slag treatment of metallurgical-grade silicon (MG-Si) was conducted, followed by acid leaching. Phosphorus-doped silicon alloy or MG-Si containing certain amounts of phosphorus and calcium was reacted at 1723 K and 1773 K with CaO--CaF2 of several compositions. Phosphorus removal from the molten silicon into the slag phase was confirmed by reduction to phosphide ions, P3-, and phosphate ions, P3-. These ions were separately determined using a wet chemical analysis method developed by ourselves. The highest phosphorus distribution ratio obtained was 2. 7 after reaction for 18 h with 17.5 mass% CaO--CaF2 slag. We then conducted acid leaching of the silicon and achieved removal of a large fraction (over 90 % ) of the phosphorus, which was much higher than that obtained by ordinary oxidizing slag treatment.IntroductionIn recent years, the production of solar cells has been increasing rapidly. Because of this, the demand for solar-grade silicon (SOG-Si) has also been growing rapidly. The development of lower-cost mass production processes is therefore needed to provide silicon feedstock. Phosphorus is one of the impurities in metallurgical-grade silicon (MG-Si). Because of its large segregation coefficient (kp = 0.35) [l ], it is difficult to remove phosphorus using a solidification refining process. Vacuum melting is considered to be a promising method for removing phosphorous from MG-Si [2], but the issues of high cost and large energy consumption have still to be resolved.Slag treatment is often used to remove impurity elements by oxidizing reactions during general oxidation refining processes. For example, phosphorus in molten steel is removed into a slag phase as phosphate ions, PO4 3-l-, by the following reaction:"

Jan 1, 2013

By George H. Edwards

Most cullets consumed in large-volume glass manufacturing processes receive little processing beyond crushing. But lead-glass cullets for specialty glasses such as industrial lighting refractors or cathode-ray tubes are combined with metals and various coatings that prohibit their direct recycling into the glass-melting processes that created them. In many cases, the contained lead renders these cullets hazardous. At present, virtually all industrial processes to separate one cullet from another depend on hand sorting, and thus are necessarily costly per unit weight. Lead-glass cullets of differing lead content are of interest because they offer the possibility of separating one glass composition from another by high-speed, automated processes at low cost. A potential process for comminution, cleaning, and separation of lead-glass cullets would involve primary and secondary crushing, magnetic and other metals separation, attrition scrubbing in water, separation of glass types by gravity techniques, drying if necessary, sampling, and preparation for transport to the point of use. Process water would be filtered to remove finely divided coating materials and glass, and reused. If carried out on a scale similar to a specialty industrial mineral processing plant, the cost per unit weight of such processing should be substantially less than the raw material value of the cullet in specialty glass production. The added value of avoiding waste disposal costs makes this process economically attractive.

Jan 1, 1994

By Chai Liyuan

Chromium-containing slag was detoxified by the method of microbial treatment using Ch-1bacteria isolated from nature by our research group, belonging to achromobacter sp. and with the characteristic of reducing high concentration of Cr(VI) in alkaline solution. The detoxifying process of Ch-1 to chromium-containing slag was studied by column-leaching techniques respectively. The results indicate that Cr(VI) in leachate can not be detected when chromium-containing slag has been column-leached for 7 days, and Cr(OH)3 content in precipitate is up to 32.8% with great value of resource recycling. Flowchart of engineering experimentation was ascertained based on the parameters of column-leaching experiments. Using the technique of pelletization of chromium-containing slag heap-leaching by Ch-1,the leaching rate of water-soluble Cr(VI) existing in chromium-containing slag reaches up to 100%, while the leaching rate of full chromium is up to 90%, when the process has been operated for 7-10 days under the conditions of 25-40C and consecutive spray by circular leachate. The content of Cr(VI) in chromium-containing slag after detoxified meet the national identification standard for extraction procedure inxicity for hazardous wastes(GB5085-1996) in China, moreover approximately 90% of Cr(VI) existing in chromium-containing slag has been recycled.

Jan 1, 2006

By Oleg I. Platonov

The process for desulfurizing coke oven gas in a regenerative system ?scrubber-stripper?, with sour gas being fed to Sulfur Recovery Unit (SRU) and tail gas being recycled to raw coke gas scrubber, has been developed. A key problem of this process is the presence of elemental sulfur in the SRU off-gas, which may deposit on gas-blowing equipment, thus disrupting its operation. A new treatment technology for SRU off-gas that has been worked out for a Claus unit operated by «Russian Metallurgical Company» (RMC) in Magnitogorsk (Russia) is presented. It incorporates a catalytic hydrolysis/hydrogenation stage, where all sulfur-bearing species such as sulfur dioxide, carbonyl sulfide and elemental sulfur are converted to hydrogen sulfide. The SRU in Magnitogorsk comprises three main units: gas re-heater; catalytic hydrolysis reactor and waste gas cooler. Re-heater is required to increase temperature of the process gas up to a level of catalytic conversion (beyond 330-3500C). Oxygen utilized as an oxidizing agent reduces the volume of waste gas to a minimal possible value. The operational data garnered since 16.07.2004 clearly shows that the new technology allows high-level purification of Claus tail gas from elemental sulfur. Unlike SCOT ? process, this technology does not require separate stages for H2S removal and enrichment that tangibly simplifies its implementation at lower capital and operation expenditures.

Jan 1, 2006

By Zachery Zanetell

Flotation circuit performance has become increasingly more challenging due to the complexity of available ore sources. To optimize value mineral recovery, the mineralogical composition of the ore should be evaluated and understood. Utilizing a variety of mineralogical and analytical tools, flotation processing challenges can be overcome and potential limitations understood. In this paper, several case studies will be discussed in terms of the value that has been provided through the use of mineralogical analysis to optimize flotation performance.

By B. W. Lightfoot, Neill F. Arthur

"The AusIron process is a new development of the well established Ausmelt bath smelting technology(l). The development of this technology has been tied to the South Australian Steel and Energy (SASE) project which brings dedicated coal and iron resources together with this new technology. SASE is a joint venture between Ausmelt (40%), Meekathara Minerals (40%) and the South Australian Government through Mines and Energy South Australia (MESA) (20%). It will use a multiple lance furnace to process iron ore using steaming coal for both fuel and reductant.It is intended to build the simplest plant economically possible. Refinements such as preheating and prereduction of the ore are compatible with the technology but are not expected to be necessary in the first generation plant.The joint venture is negotiating with suitable partners for funding of the project through to commercial implementation at a target scale of2.5 mt/a of pig iron.ObjectivesAusIron aims to produce pig iron directly from steaming coal and from any of a variety of iron sources in a simple furnace system with a minimum of pre-processing of either coal or iron ore. Preheating and prereduction of ore are compatible with the technology but may not be necessary. The immediate aim is not to be the technology that uses the least quantity of coal to produce iron metal but rather the technology that uses the least number of dollars to produce metal.The chemistry of iron making is well known, probably better known than that of smelting of any other metal. Iron has been made for thousands of years and it is possible to make iron from charcoal and ore in a simple blast furnace the size of a beer barrel. The focus is therefore not making iron but rather making it more cheaply than it is made by current technologies. Large blast furnaces now set the standard and new technologies must perform better if they are to gain market share. It is still the cost of iron, energy units and capital going into these mega blast furnaces which ultimately set the market price for pig iron."

Jan 1, 1996

By S. W. Ip

Over the years, the importance of surface and interfacial phenomena has been neglected by the copper-nickel industry. As a result, little data on the surface and interfacial tension of the Ni matte and slag system are available in the literature. In view of the scarcity of information in this area, the surface tensions of the Ni-Fe-S system together with the Ni-Fe-S and fayalite type slag system were measured using the sessile drop technique. Drop images were obtained by X-ray radiography. For the Ni-Fe-S system, the results showed that the surface tension of the matte increases with matte grade. The surface tension behavior with changing matte grade showed a slight negative deviation from ideality. This indicated that FeS is slightly surface active in the nickel matte system. Results also indicated that small increase in sulphur content in the matte can decrease the surface tension quite significantly. The measured surface tension of the Ni-Cu-S system showed a linear relationship with the Cu2S content in the matte. The surface tension decreased with Cu2S content. Interfacial tension measurements showed a similar trend. That is, interfacial tension increased with increasing matte grade. The presence of MgO (-1.5%) and A12O3 (-6%) in the slag does not affect the interfacial tension value. Effects of matte surface tension on phenomena such as entrainment of matte in slag and infiltration of matte into refractory pores are discussed. The calculated flotation coefficients indicated that flotation of nickel mattes cannot be avoided by changing the matte grade. Filming of matte on bubbles can occur below a matte grade of about 19% Ni3S2. As for infiltration, refractory bricks containing high Cr2O3 will be easily wetted by matte regardless of matte grade. Therefore, bricks containing high Cr2O3 can easily be infiltrated by liquid matte.

Jan 1, 1993

By A. McLean, S. Dawson, N. D. G. Mountford

"IntroductionIn order to predict the accepted industrial practice for the year 2000, it may be helpful to first consider the rate of development of scientific knowledge. If the speed with which man can travel on commercial vehicles is taken as a criterion for determining the rate of progression, then it can be seen from Figure 1 that advancement in our present century is very rapid. Likewise, if computer technology is used as a criterion for the measurement of scientific advancement, it becomes evident that technological evolution can be highly exponential. These two examples are sufficient to demonstrate that engineers and managers cannot afford to regard scientific development as being linear with respect to time if they are to avoid underestimating the needs of society.Within this framework of overall development, the time required for individual ideas to progress from inception to regular application has decreased considerably. For example, X-rays first discovered by Roentgen in the 1890's and now used widely in medicine and engineering, required a developmental period of some eighty years. The motorcar evolved from early beginnings at the turn of the century to a position of great social impact in sixty years. Rectifier materials used in high frequency radar to the present explosion in communications, required forty years. As illustrated in Figure 2, the period is shortening rapidly.The use of sound waves appears to be following a similar path. There is now a considerable body of knowledge concerning their behaviour and exceptional advances have been made. In medicine and engineering the sonic approach to examination is well established, and acoustic testing forms the basis of several diagnostic and quality control applications. With respect to metals engineering, ultrasonic testing has contributed to the understanding of the relationship between the size and number of internal defects and the probability of premature failure. This has allowed the designer to incorporate appropriate safety factors in his designs; but more importantly, the realization of the deleterious effect of inclusions on the performance of the final product has resulted in a continuous pressure on the material suppliers to reduce the number of defects in their products.It is not only the designer who is demanding defect free material but also the fabricator, as material breakdown during manufacture can be prohibitively expensive. Examples of this can be found in both the aluminum and steel industries where ultra clean sheet is required to ensure that rejections are minimized during beverage can manufacture and other deep drawing operations."

Jan 1, 1988

By Ryosuke Matsuoka

Keywords: Tantalum capacitor, Scrap, Recovery, Titanium, Chlorination A recycling process for tantalum from capacitor scraps using an oxidation process followed by mechanical separation and chemical treatment was investigated. This study demonstrates that sintered tantalum electrodes inside the capacitor scraps can be mechanically collected after the oxidation of the scraps in air, and high-purity tantalum oxide powder (Ta2O5) was efficiently recovered after chemical treatment. By reducing the Ta2O5 obtained through magnesiothermic reduction, tantalum powder with 99 mass-% purity was obtained. Using the chlorination for tantalum recovery was also investigated, and the tantalum or tantalum compounds were reacted with chloride wastes such as FeClx. It was found that tantalum was effectively separated and purified when tantalum powder is reacted with FeClx at 1100 K under an argon atmosphere. This recycling process utilizing chloride scrap has now been extended to other reactive metals such as titanium.

Jan 1, 2004

By Qixing Yang, Björn Haase, Fredrik Engström, Anita Wedholm

"MiMeR, the Minerals and Metals Recycling Research Centre at Luleå University of Technology, Sweden, started industry-related research work to stabilize an EAF slag from Höganäs AB with of CaO/SiO2 values near to 3.2. The intention was to determine the suitability of the EAF slag as construction material after stabilization. Some of the stabilizers effective for preventing disintegration of AOD slag were examined in laboratory tests for stabilization of the EAF slag. The EAF slag samples were mixed together with stabilizers for melting at 1600ºC and then cooling in a crucible system. With a laboratory granulation system, the liquid EAF slag was cooled rapidly using air. Samples from the tests were characterized by different techniques, including XRD and SEM. Some of the results from the work may be useful for preventing slag disintegration and, thus, enhancing utilization of the EAF slag as construction material, thereby saving valuable natural resources.IntroductionAt steel plants of some MiMeR member companies, steel grades with low carbon contents were produced in Electric Arc Furnaces (EAF). EAF slag was tapped out of the furnace to slag pots for transport to slag yards, where the slag was poured on the ground. Very often, the EAF slag disintegrated during cooling on the ground. Fines from the slag disintegration were often difficult to handle and use as material for road construction [1, 2]. The EAF slag disintegration was rather similar to the disintegration occurring in the slag tapped from some AOD (Argon Oxygen Decarburization) converter heats.Literature studies show that formation of dicalcium silicate (C2S) is the main reason for the disintegration or dusting of AOD slag from production of stainless steel [1-4]. The C2S can form while the content ratio of CaO to SiO2 of the slag, CaO/SiO2, exceeds 1.4 [1]. Values of CaO/SiO2 for the AOD slag are often near to 2.0, making the C2S a predominant slag component. The ß phase of C2S, ß-C2S, transforms into its low temperature ? form in the temperature range of 400-500°C, inducing a volume expansion of nearly 12% [1-4]. The volume expansion disintegrates the AOD slag."

Jan 1, 2008

By Melvin A. Jennings

Ion-exchange technology for precious metals recovery is at a turning point. Some very exciting technology has been developed in the past five years which should lead to commercialization of the process. Ion-exchange will allow not only for the recovery of gold and silver, but also will allow for the recovery of cyanide form plant tailings. This process may soon be competitive with Merrill-Crowe for silver and once this occurs, it will become the process of choice.

Jan 1, 1991

By Gus Van Weert

This paper describes the results of autoclave testwork where ferric nitrate was hydrolysed in the presence of certain cations and anions and the resulting hematite analyzed for foreign constituents. For the cations Zn++, Ni++, Cu++, and AI+++, selectivity factors of over 107 were found. Magnesium gave 3.106. These factors are calculated as Me/Fe in solution over Me/Fe in the hematite; Me representing the metal in ion added. As-a result of the testwork at Delft University of Technology, BUDELCO (the Netherlands electrolytic zinc producer) ran a series of ferric nitrate hydrolysis tests in the presence of 10 additional trace elements. Impurity levels were prejudiced on Me2 EPHA extraction of iron from their zinc circuit, followed by HNO3 stripping. Good selectivity against base metals was confirmed, but trace elements forming anions (As. Sb) and sulphate were incorporated in the hematite. These BUDELCO results are also presented.

Jan 1, 1995

By J. Partinen

Drying is a unit process which has numerous applications in metallurgical process industry. Kumera Technology Center, being a worldwide equipment and process supplier, has developed sophisticated solutions for both direct and indirect drying. In conventional direct drum drying, the energy is taken from combustion of fossil fuels, requiring energy input and emitting considerable amount of off gases. In modem copper smelters, thermal energy from the off gases is recovered in waste heat boilers making the steam available. Using that steam as the energy source for concentrate drying, the total volume of off gases can be considerably reduced and releasing of harmful combustion gases into the atmosphere can be avoided. Kumera Technology Center has recently developed and promotes a new steam drying process for drying of copper concentrates. In the development of the new dryer, Kumera's approach has been to combine the best properties of both the steam dryers and the drum dryers. In the design special attention has been paid to overcome problems of excessive wear and clogging and to reduce the required maintenance operations. In this paper the environmental issues and energy consumption related to both direct and indirect drying processes are discussed. The estimated operation costs and emission levels are compared, based on calculations and the data collected from industry. Finally, the development project of the Kumera Steam Dryer is briefly reviewed

Jan 1, 1999