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By Garry W. Warren

The brass foundry industry produces a significant amount of waste sand containing Cu, Zn and Pb which is often classified as a hazardous waste due to Pb content. The potential application of a hydrometallurgical process to treat the sand by extracting metal values and thus detoxifying the material has been investigated. The process involves leaching of metal values followed by cementation. The emphasis of this investigation was on the leaching step, although some preliminary cementation experiments have been performed. In order for any alternative treatment scheme to be successful, the smaller size fractions of the sand must be addressed. Experiments have been performed on five individual size fractions using various lixiviants HCI, acetic acid and HCI/NaCI. Cu extraction was found to be slower than either Zn or Pb. Results obtained in this investigation indicate that copper is present in two forms, an oxide form which dissolves rapidly and is insensitive to the level of oxygen, and a less soluble form, probably metallic which dissolves more slowly and requires an oxidizing agent. The presence or absence of oxygen had no influence on the rate of Zn dissolution indicating that zinc is present mostly in oxide form. Toxicity Characteristic Leaching Procedure (TCLP) tests showed that residues could be produced which meet the toxicity limit for lead. Preliminary cementation experiments have also demonstrated the feasibility of Cu and Pb recovery.

Jan 1, 1991

By Maria D. Salazar-Villalpando, Anthony Cugini, Bryan Reyes

"The electrochemical reduction of CO2 was performed in a laboratory-made, divided Htype cell. A copper electrode was used as the cathode. An Aldrich Nafion 117-type ion exchange membrane (0.18mm thickness) was used as the diaphragm. NaHCO3 and KHCO3 were studied as the catholytes. Hydrogen evolution from water reduction and products from CO2 electrochemical conversion were recorded. Higher CO2 reduction enhancement was observed by KHCO3 as compared to NaHCO3. The main conclusion of this work is that in fact CO2 can be electrochemically reduced with copper electrodes.1.-INTRODUCTIONThe direct electrochemical reduction of CO2 may allow for a simple process and, by avoiding high temperature reactors, would enable the process production rate to be quickly varied to follow the time of day availability of surplus electricity [1]. Temperature has a major effect on the electrochemical conversion of CO2 since its solubility increases when temperature decreases [2]. The electrical potential applied to the electrochemical reacting system will have an influence on the product distribution, as well. For example, a narrow potential range during cyclo-voltagraphic studies will determine the detection of a lower number of products. A recommended potential range to study the electrochemical reduction of CO2 is -2V to 2V. Moreover, the reaction rate on the electrode is governed by various processes, such as the kinetics of electron transfer, adsorption/desorption at the electrode surface, and diffusion of CO2 to the Cu electrode. The availability of active species, CO2 for electro-reduction, is extremely low at the vicinity of the electrode surface and it seriously interferes with the rate of mass transfer. In batch type electrolytic reactors, depletion of CO2 at the surface takes place first. CO2 from the bulk then has to diffuse to the electrode surface, resulting in mass transfer controlled kinetic phenomena. During the above process, several other competitive side reactions could suppress the primary reaction even though the cathode has good electro catalytic properties for reduction of carbon dioxide. When the dynamic supply of specific active species is ensured to electrode surface, the mass transfer effects are minimized to certain extent. Hence it is envisaged that a continuous flow reactor is more efficient for the electro-reduction of CO2 in CO2 saturated aqueous electrolytes. The primary reactions that occur at the copper electrode during the reduction of CO2 are listed below (with the standard potentials calculated using formation energies [1] :"

Jan 1, 2010

By Carl C. Nesbitt

A study was conducted to investigate the claims of early observers who noted an increase in the rate of gold dissolution when chlorine was chemically produced in the leach vessel compared to sparging with chlorine gas. This "nascent" chlorine was presumed to be an active intermediate in the production of chlorine (C1,l from chloride ions. The study used UV light to produce an activated chlorine atom intended to recreate the observed increase in the gold dissolution rate. Although no change in the kinetic rate was observed, the reaction mechanism by which chlorine reacts with particulate gold was instead determined. Various concentrations of multivalent cationic chloride salts were added to the leach solution to demonstrate that the increased dissolution rate was due to the increased concentration of the chloride ion and ionic strength of the solution.

Jan 1, 1992

By J. Michael Canty

Over 25 years of US research in Mineral Recovery from Geothermal Solutions have lead to few commercial applications. With the World Bank program in Kamchatka, Russia in September 2005 a step was taken to vitalize and coordinate the many efforts to advance economic mineral recovery systems worldwide. The US Department of Energy is helping to spur on the interest and research needed to realize the many benefits of extracting minerals from geothermal solutions. The excitement of recovery of minerals from geothermal brines has many positive angles. The economics of certain geothermal site is improved if a revenue is arrived from a sellable commodity with the geothermal power. The use of cleaner geothermal brines also improves the capable use of the brine before reinjection. We will review the history of Geothermal in the USA and the opportunities for recovery of different minerals and the markets for them.

Jan 1, 2006

By Sylwia Zymankowska-Kumon, Rafal Danko, Józef Danko, Mariusz Holtzer

"Burning of ceramic materials is carried out at temperatures 900+ 1300°C, in dependence of the required functional properties. The Faculty of Foundry Engineering together with the Faculty of Material Engineering and Ceramics developed the technology of production of burned ceramic materials with using spent moulding and core sands. The mentioned above waste materials of the foundry industry fulfilled -in plastic masses intended for obtaining ceramic materials -the role of the addition weakening clay raw materials. The laboratory investigations were fully verified by the results of industrial tests. It should be pointed out that none negative effects were observed at the stage of mixing raw materials and preparation of plastic masses. The measurements of exhaust gases emissions performed during burning the products containing spent moulding sands as well as during the normal production did not exhibit any significant differences, which could have indicated the harmful impact on the natural environment.IntroductionSands are used by the foundry industry to make metal casting molds and are a mixture of silica sand, bentonite clay and carbonaceous additives or resins. During the casting process, the molten metal cause thermal decomposition of carbonaceous additives or resins, which results in the formation of potentially hazardous organics, that are emitted to the atmosphere and condense in the molding sand. Each year the U.S. foundry industry landfills about 10 million tones of sand because it is no longer suitable to make metal casting molds. A large high-silica sand content in spent foundry sands (SFSs) generates rational premises for their reuse in other than foundry practice fields. Efforts to divert the SFSs from landfills and encourage their beneficial use in manufactured soils, geotechnical applications, the construction industry (road construction, highway construction), the building materials industry (cement, bricks, limestone manufacture), in the filling of mining cavities or in landfill construction (roads on landfills, permanent covers) are make [1-7]."

Jan 1, 2013

By Carl W. Dalrymple

A wide variety of contaminants (heavy metals, suspended solids, colloids, oils, organics) have been successfully removed from wastewater using an electrocoagulation process. An innovative electrocoagulation system is described. This process involves a procedure which subjects dissolved and suspended wastewater contaminants to the simultaneous addition of metal ions in the presence of direct current. During the treatment process Ionic and other charged particles in the wastewater are neutralized with oppositely charged ions generating the coagulation of contaminants: The process Is called CURE, and' presented here with application to wastewaters containing mainly heavy metals.

Jan 1, 1995

By Michael L. Sorokin

The metallic nickel production by converting of nickel matte is analysed from the thermodynamic point of view using earlier developed thermodynamic models for sulphide, metal and slag phase. Three-suffix Margules equations are used to calculate thermodynamic properties of melts. Potential diagrams of Ni-FeS-OSiO2 system are calculated for various temperatures and Fe to Ni ratios. The diagrams used for consideration about possibilities of the direct one-stage metallic nickel production.

Jan 1, 1995

By M. C. Ruiz

This work outlines the results of leaching studies on a copper concentrate containing chalcocite (Cu2S) and digenite (Cu9S5) with an acid saline solution of cupric chloride oxygenated at ambient pressure. The variables studied included the stirring speed, concentration of cupric ions, concentration of HCI, concentration of chloride ions, oxygen flow rate, temperature and time. The leaching system was found to be very effective for the dissolution of the concentrate. Over 95% of the copper was dissolved in 30 minutes with negligible dissolution of iron. The dissolution of copper increased with the stirring speed up to about 400 rpm and depended little on the total chloride concentration. The oxygen flow rate affected the dissolution of copper only below 0.1 1/min. The concentration of HC1 did not influence the dissolution providing its was sufficient to avoid the precipitation of copper oxychloride. The study of the effect of the temperature showed a maximum in copper dissolution around 90 "C

Jan 1, 1997

By Stephen R. Brown

Current conditions in the copper market demand that mine and plant operators make budgeted production targets at the lowest possible unit costs. For those companies bringing new production capacity on-line, achieving budgeted production levels as quickly as possible after start-up is vitally important to minimize unit costs and to begin a positive cash flow. Whether the objective is to simply improve unit costs or successfully start-up a new, complex plant, success will be strongly influenced by .the skill levels of the operators :and supervisors. The only way to assure return on plant investment, and to survive during depressed metal prices, is to ensure that plant operators have the knowledge to effectively run the plant. Technology available in computer-based, multimedia training systems, including: interactive animation, videos, voice-overs, schematics, and text can now be used to train operators at their own pace using plant-specific information. Additionally, it has been shown that learning through multimedia provides a higher degree of long term retention than more traditional learning methods.

Jan 1, 1999

By M. Cassir

"The unique properties of molten carbonates offer a large scope of applications in the field of energy. In effect, these molten salts are in the center of chemical and electrochemical reactions involving carbon and carbonaceous species, carbon dioxide and carbon monoxide, significant for energy generation or even for the production of fuels. Moreover, such media have also an oxidative character; they dissolve molecular oxygen and oxygen reduced species, O 2-, O22- and hypothetically o-, which may have an important role in waste treatments, homogeneous catalysis and synthesis of oxides. In this presentation, an overview will be given on the principal physicochemical properties of molten carbonates, before focusing on their main known application, the molten carbonate fuel cell (MCFC). Progress in other new fuel cells applications will also be analyzed, such as direct carbon fuel cell (DCFC), hybrid carbon fuel cell (HDCFC) and composite high-temperature fuel cells combining the features of MCFC and solid oxide fuel cell (SOFC). Afterwards, membranes for the separation and capture of C02 will be reviewed. Finally, other topics, as the oxidative coupling of methane in molten carbonates, will be briefly mentioned.IntroductionIn the thirty past years, the molten carbonate science and advances have been mainly dedicated to the understanding and optimization of the molten carbonate fuel cell (MCFC), which is still a major issue in the heart of a new vision of energy development. More recently, new topics related to other kinds of fuel cells (DCFC, composite SOFC/MCFC systems) and C02 capture have emerged and are concentrating important research and technological efforts. Moreover, new fields of implementation, related to molten carbonates, are also present: geology, glasses, production of nanocarbon particles etc. Considering other areas where this molten phase plays a major role, such as catalysis, waste destruction, surface treatment, it can be confirmed that the field of molten carbonates is very rich and offers many opportunities for fundamental science and competitive applications. Whatever their specific application, molten carbonates activity is associated to more efficient energy systems with low production of C02 and, in a prospective sense, to non-polluting energy using the value of C02. A recent event, the International Workshop on Molten Carbonates & Related Topics, IWMC201 I, held in Paris in 2011 , have put in evidence the importance to improve and exploit this investigation and technological domain."

Jan 1, 2012

By R. Harris

Blister copper melts of 800 g to 1000 g containing less than 1 wt % S and up to 3 wt % Ni were desulfurized at 1523 K in air or by a pure oxygen jet blown at 75,500 and 1000 cm3/min, from 1 cm above the melt. Rates of desulfurization and oxygen pickup were measured and visible surface phenomena were photographed and videotaped. It was observed that SO2 was evolved from Cu-S melts in a manner reminiscent of the effervescence seen in carbonated drinks. The effervescence lasted up to 20 minutes and resulted in the ejection of material up to a height 50 cm above the melt surface. Sporadic discharge of large bubbles was also observed in a Ni containing melt top-blown with oxygen at 1000 cm3/min. The Cu-S melts top-blown with oxygen experienced faster sulfur elimination as compared to stagnant melts exposed to air and experienced only a single period of turbulent SO2 evolution, which occurred almost immediately after oxygen injection commenced. The Cu-S melts exposed to air experienced multiple episodes of effervescence. The stagnant blister copper melt containing nickel did not exhibit effervescent behaviour and experienced a lower rate of sulfur elimination compared to Cu-S melts tested under similar conditions. The present article examines the role of surface phenomena in determining the observed behaviour.

Jan 1, 1999

By Xiaodi Huang, Matthew Andriese, Zheng Zhang, Jiann-Yang Hwang, Zhiwei Peng

"A simplified finite-difference time-domain (FDTD) algorithm for modeling microwave propagation in magnetic dielectric materials was developed and employed to study the microwave dissipation in magnetite. Heat transfer during microwave heating of magnetite was subsequently investigated by solving heat transfer differential equation using explicit finite-difference (EFD) method. It is observed that temperature of magnetite surface increases rapidly in the first minute due to the rapid strength decays in both electric and magnetic fields within a short distance along the path of microwave dissipation. A temperature peak, initially formed at the surface of the sample slab, migrates inward as heating time extends and microwave power increases.IntroductionAs one of primary materials in iron and steel industry, magnetite exhibits excellent microwave absorption capability, which leads to great energy conservation in microwave assisted steelmaking [1,2]. The fast temperature increase in microwave heating of magnetite can be attributed to both dielectric and magnetic losses [2]. Although much experimental work has confirmed this observation, detailed computational studies for modeling of microwave field dissipation in magnetite at commonly used frequencies, such as 915 MHz, has not been well addressed [1,3].Finite-difference time-domain (FDTD) method is widely used in computational electrodynamics modeling to simulate the dynamics of electromagnetic wave scattering from various media [4,5]. This approach requires modeling algorithm to be formulated with integration of specific characteristics of each medium. An extensive literature survey indicates that current formulations are only suitable for modeling electromagnetic waves propagating in normal dielectric lossy materials [5,6]. Since magnetite is a magnetic dielectric material in which both dielectric and magnetic properties contribute to the heating process under microwave irradiation, a specific algorithm should be developed for the simulation."

Jan 1, 2012

By C. L. Lin

Multiphase, irregularly-shaped randomly-oriented PARGEN particles were grown to determine the breakage/liberation characteristics of such locked particles. The simulated locked particles were randomly broken to establish the liberation characteristics of the broken fragments. The progeny size distributions are consistent with Gilvarry's volume and surface flaw model for single particle breakage. The extent of liberation of both continuous and dispersed phases can be described from the conservation of interfacial area. In this regard the data can be normalized and liberation described for a wide range of dispersed phase grades and dispersion densities.

Jan 1, 1988

By Osarnu Inoue

In Mitsubishi Continuous Copper Smelting and Converting Process, smelting, slag-matte separation and matte converting are continuously carried out in series in three furnaces connected by launders. As a result of this operational configuration of the furnaces, influence of the change in operating condition in upper stream, such as variation of feeds in the smelting furnace, propagates to down stream with some delay. In order to achieve stabler operation, process control algorithm based on the dynamic characteristics of each furnace would be very effective. In this study, the dynamic process simulation model was developed for the smelting furnace. The model consists of two mathematical modules, i.e. the thermodynamic module and the mixing module. The calculation results using operating data obtained at Naoshima Smelter showed good agreement with the actually observed change in temperature, composition and flow rate of matte and slag at the outlet of the furnace. In addition, operation parameters such as reaction efficiency of oxygen and coal, dead volume of melts were estimated.

Jan 1, 1999

By Runsheng Xu, Haiyang Wang, Pengcheng Zhang, Tengfei Song

Semi coke, a byproduct in the chemical industry, is a new fuel for blast furnace injection in China. In this study, semi coke and bitumite were milled into different size, ranged from 0.147mm to under 0.074mm. The content of volatile matter and ash, which affect the combustibility of semi coke, were measured using muffle furnace. The mixture, in which the proportion of coal in different sizes changed, was blend by semi coke and bitumite with different size. Activation energy calculation and the comprehensive combustion characteristic index of all kinds of blends was also discussed. The result obtained by Thermogravimetry –Derivative Thermogravimetry curves indicates that the smaller the size of mixture is, the lower for the characteristic temperature, and the better for its combustibility, Semi coke can be a substitute for anthracite in blast furnace injection.

Jan 1, 2015

By Katsuyasu Sugawara, Takuo Sugawara, Shin-ji Abe, Tadakazu Kagami

"In order to clarify the mechanism and to obtain the fundamental data for heavy metal recovery from an incinerator ash by chlorination, pure chemical reagents, zinc oxide and lead oxide or the fly ash blended with calcium chloride and silicon dioxide were heated up to 1000°C in a nitrogen stream. Thermogravimetric curves of the samples with the chlorinating reagents indicated that solid-liquid reactions accelerated the chlorination and release of metals from the solid phase. The formation of liquid phase of calcium chloride played an important role on effective recovery of zinc and lead at lower temperatures below 800 °C. Although zinc and lead could be decreased in the incinerator ash without chlorinating reagents, addition of chlorinating· reagents enables the removal of metals in high extent· at lower temperature.IntroductionFly ash is discharged about 3,000 tons/day (about 110 million tons/year) from incinerators of municipal solid waste in Japan and mostly fly ash is disposed in landfills. Fly ash includes heavy metals e.g. zinc and lead. Since untreated fly ash caused hazardous leaching problems, Waste Disposal and Public Cleaning Law was revised in 1992, fly ash being designated 'specially controlled' general waste. Fly ash must be disposed by the following suitable, intermediate four methods: [I] Cement- Solidified Method, [2] Immobilized Chemicals Method, [3] Melting Solidified Method, [4] Acid Leaching Method, permitted by the Ministry of Health and Welfare, Japan."

Jan 1, 2000

By E. L. Frueh

AMAX Base Metals Research & Development, Inc. has developed a process for treating copper-nickel mattes to produce copper cathodes and a pure nickel sulfate solution. In this process, the input matte is preleached in a copper sulfate electrolyte bleed solution so as to dissolve nickel from the matte and cement copper from solution. The preleach leaves a substantially pure nickel sulfate solution. The residue from the preleach is roasted to less than about one percent sulfur. A portion of the calcine is leached with sulfuric acid to make a copper sulfate solution for input to the tank house. The residue from this leach and the remaining calcine are smelted to form a bimetallic (copper/nickel.) anode. The anodes are electrolytically refined and copper is preferentially deposited on the cathode while the nickel reports to the electrolyte, A bleed stream is taken from the electrolyte and used in the preleaching of the input matte. This process produces high purity metal streams while consuming less energy and smaller amounts of reagents as compared with other matte processes.

Jan 1, 1983

By Alexander A. Knminskii

Polymorphism of BaR2F8 compounds is analyzed, and some peculiarities of obtaining monoclinic low-temperature (3-BaR2F8 crystals (R=Y, Ho-Yb) and orthorhombic high¬temperature a-ßaR2F8 crystals (R=Yb, Lu) by the Bridgman-Stockbarger growth technique are discussed. We pay a special attention to BaYb2F8:Er3+ crystals, which are able to generate both 2:µm SE using the new four-level operating scheme (4F9/2?4I11/2 laser channel) and 2- and 3-µm SE by means of the cascade scheme (4F92?+4I11/2?+4I31/2). This 2-µm generation of Er3+ ions has an advantage over similar SE of Ho3+ and Tm3+ ions (especially under diode laser pumping), that is important in designing the medicine and ecology laser. We report on orthorhombic BaR2F8 crystals with the ordered structure, a new crystalline materials for generating Ln3+ ions. The growth conditions are determined and orthorhombic BaLu2F8 crystals of several cm3 in volume doped with Ce3+, Nd3+, Ho3+, Er3+, and Tm3+ ions are obtained for the first time. Spectroscopic and laser characteristics of these crystals are discussed for Nd3+-and Era+-doped samples serving as representative examples. In particular, low-threshold stimulated emission was excited in 4F3/2?+4I11/2 channel of Nd3+ ions in the BaLu2F8. Room-temperature generation was obtained also at -1.317 µm wavelength for Nd3+ and at ~2.8 µm (several lines) for Era+ ions in this new laser crystalline host with a threshold of about 20 J.

Jan 1, 1997

By Aichun Zhao, Rui Wang, Yihong Li, Yanping Bao, Yafeng Ji, Jiansheng Liu, Xiao Hu, Qingxue Huang

The slag entrapment under different conditions of 80t blowing argon ladle furnace was investigated by physical simulation. The water was used to simulate liquid steel and liquid paraffin was for slag. The processing of slag entrapment under different blowing structures was analyzed and the critical velocity and critical droplets diameter of describing it was obtained. Based on the experiments, the relationship between the interface flow velocity and the critical blowing rate CBR was deduced. In the real process, it is suggested that the bottom blowing rate is from 40 L/min to 180L/min when the interface tension is 0.12~1.2 N/m during the soft argon blowing.

Jan 1, 2016

By Kenji Morinaga, Hiromichi Takebe

"Ge-S binary glasses in the range 57 to 90 at %S at 0.5 to 3 at %S intervals were prepared by a conventional melting technique using fused quartz ampoules as melting containers. Impurities contaminated during preparation process are evaluated by IR spectroscopy. The causes of impurity contaminations are discussed. Density data in a systematic series of Ge-S glasses is demonstrated. IntroductionSulfide glasses are of particular interest for new laser and nonlinear optical materials in the near-infrared and infrared regions [1]. Sulfide glasses have the features of low-phonon-energy and high refractive index with moderate rare-earth ion solubility. The low-phonon-energy is favorable for the reduction of nonradiative rate for the emission of rare-earth ions. The high refractive index results in a high radiative-rate and in a high third-order nonlinearity. However, impurities may degrade the superior optical properties of sulfide glasses.In this work Ge-S glasses were prepared by a conventional melting technique. Impurities contaminated during the preparation process are evaluated and their causes are discussed for future improvements. The measured densities of Ge-S glass samples were compared with the results of previous studies [2], [3]. Ge-S glasses have some favorable properties for practical .applications including non-toxicity, good thermal and chemical stabilities."

Jan 1, 2000