Search Documents

By Staia. Mariana H.

Thermochemical equilibria of the heterogeneous system Ti-N-H-CI-Fe-Cr-Mo-Ni-Mn-C were calculated by using a commercial software based on the minimization of the free energy. Equilibrium calculations were done for temperatures varying between 800" and l 100°C and an initial molar relationship between reactants, a=NJTiCI,, of 0.1 to 2. The deposition process was considered to occur at atmospheric pressure. The activities of the alloying elements of the stainless steel were considered equal to their molar fractions. It was shown that for the conditions studied the substrate is no inert with respect to the gaseous phase. The existence of liquid chlorides was predicted for temperatures between 800" and 850°C and a ratio between 0.3 and 0.9. The most important metallic chlorides which appears to be present from the calculations in appreciable quantities in the gaseous phase are iron dichloride and manganese dichloride. In the low-temperatures zone and for low initial nitrogen contents, it result that the appearance of the liquid chlorides seems that partially inhibits the production of gaseous HCI. The highest deposition process efficiency calculated is obtained at a temperature 2 900°C and a N2/TiCI, ratios 2 0.7.

Jan 1, 1995

By I. J. Moon

The reduction behavior of hematite by H2 and H2-CO gas mixtures was investigated to elucidate the reduction mechanism at 800-950 °C. The hematite compacts were made by Cold Isostatic Pressing to produce compacts of uniform shape and size. The compacts were sintered at 1000° C for 30min, and showed a contraction of 29%. Mercury pressure porosimeter was used for measuring the total porosity, pore size distribution and pore surface area of the compacts. Reduction was measured by means of weight-loss technique using Cahn Balance (Model : TG-171, capacity log, accuracy f 10pg). Microscopic examination and X-ray analysis were used to correlate the structure of reduced compacts with the mechanisms of reduction. Neither chemical reaction control nor diffusion control is adequate in describing the complete course of reduction of the hematite compact. The reduction of hematite compacts was initially controlled by the chemical reaction at oxidelmetal interface. The reaction goes through a transition phase .where it is undergoing a mixed control, followed by the diffusion control towards the end of the reduction. The values of apparent activation energies for chemical reaction control were 3.48-8.43 kcal/mol depending on the gas compositions.

Jan 1, 1997

Based on experimental and computer simulation results from our group, we report a systematic, atomic level analysis of carbon dissolution from carbonaceous materials in molten iron. Experimental results on graphite/Fe-C-S system were obtained using carbon dissolution studies, XRD and FESEM investigations and were supplemented with Monte Carlo simulations. Three basic mechanisms, namely carbon atom dissociation rate, interfacial phenomena and mass transfer in the melt were found to be responsible for the overall dissolution process. While mass transfer in the melt is governed by the concentration gradients, melt composition and temperature; impurities present in ash play a significant role in the interfacial phenomena. For less ordered forms of carbonaceous materials, carbon atom dissociation rate depends strongly on the degree of long-range order and is an important rate controlling mechanism in the overall dissolution process. A systematic comparison of dissolution rates for a variety of coal-chars, natural and synthetic graphites has been carried out in an attempt to identify rate-controlling mechanisms. The structure of the carbonaceous material appears to be an important underlying factor in the carbon dissolution process.

Jan 1, 2003

By Norihiro Murayarna

Hydrothermal synthesis of K type zeolite was carried out by using coal fly ash as a raw material and KOH as an alkali source. The change in various physical properties of the obtained zeolite, such as the kind of zeolite crystal, cation exchange capacity, surface structure of zeolite and particle size distribution were investigated through the overall reaction of zeolitization. The reaction mechanism of K type zeolite from coal fly ash was investigated from these results in this study

Jan 1, 2002

By T. T. Chen

Copper anodes generated from copper scrap are relatively rich in Sn, Zn and Fe. Because of the presence of oxygen, only trace amounts of Sn occur in solid solution in the copper crystals. Thus, Sn occurs mainly as SnO2, Cu-Sn-Ni oxide and Sn-Ni-Zn oxide in the copper anodes, and Zn and Fe occur mainly as minor constituents in the Sn-Ni-Zn oxide and Cu-Sn-Ni oxide. During electrorefining, these oxide species are liberated from the copper anodes and report directly to the anode slimes. The trace amounts of Sn present in solid solution in the copper crystals dissolve but reprecipitate as Sn arsenate or a Sb-As-Sn-O phase. Accordingly, high Sn contents in copper anodes do not lead to elevated Sn concentrations in the electrolyte.

Jan 1, 2010

By Chen Song

Cobalt basic carbonate particles were precipitated from 1.0mol cobalt nitrate or cobalt sulfate solution with ammonia carbonate. By controlling the zeta-potential of the particles and the ionic strength of the solution, the uniform particles with ellipsoid or rod shapes were obtained. During the precipitation process, the interface tension was diminished to the minimum and therefore the Ostwald ripening and secondary nucleation were both inhibited. The morphology and the size control by zeta-potential seem to be the result of thermodynamics rather than classical crystalline kinetics. The particle sizes were in the range of 0.4-0.6, 0.3-0.4 micrometer. After thermolysis, the spinel-type C0304 particles were produced. The morphologies of C0304 particles were similar to that of their precursors.

Jan 1, 2003

By Mikio Kobayashi

Extraction of valuable metals from sulfide ores continues to be a very important, process and so the strict control of discharge of harmful metals in effluents from refineries becomes more important in the future. The recovery methods for heavy metals have been developed. Some metals such as Se and As are still difficult to be removed to very low concentration, although the techniques for recovery and removal for many kinds of heavy metals have already been developed. Especially, in case of Se the recovery system from water with low concentration has not be developed yet, although the WHO decided Se to be harmful for human beings and then the discharge control is under obligation now. In general Se exists as selenite ion and/or selenate ion in aqueous phase and selenite ion is able to be recovered by coprecipitation with ferric hydroxide or by reduction to solid selenium by general reductants. Selenate ion, however, has a strong resistance to conventional treatments. Therefore the new technique for the recovery of Se from water including selenate ion has to be developed. In this presentation the new approach for removal of selenate ion using the reaction in which ferrous ion is oxidized to ferric ion is presented. Selenate ion is reduced to selenite ion during the reaction and then to solid selenium, while ferrous ion is oxidized to ferric ion. The coexistence of activated carbon is very useful to increase the reaction rate. The use of iron powder is also effective and very useful for reducing gel-like precipitates mainly consisted of ferric hydroxide. The concentration of the residual selenate ion is probably under 0.1 ppm after recovering Se by the mentioned-above approach. In addition to the mechanisms of these reactions, the effects of pH, coexistent positive and negative ions, and reaction temperature are also presented. Furthermore the investigation of the behavior of selenosulfate is presented.

Jan 1, 1998

By Yongqi Sun, Zuotai Zhang

Our study investigated the influence of P2O5 and B2O3 on the viscosity and crystallization behavior of Ti-bearing blast furnace (Ti-BF) slags for the purpose of Ti extraction. The investigation of the crystallization behaviors were carried out using a single hot thermocouple technique (SHTT) and the viscosity was obtained by rotating cylinder method. For the viscosity, the results showed that P2O5 substantially increased the slag viscosity. P2O5 is a network-forming oxide, which increased the degree of polymerization of slags and accordingly increased the slag viscosity. However, both of slag viscosity and apparent activation energy for viscous flow remarkably decreased with B2O3 addition. As a typical network forming oxide, B2O3 was introduced into the network and existed dominantly as 2-D structure, BO3 triangular, which caused a simpler structure and a decreasing slag viscosity. As for the crystallization behaviors of Ti-BF slags, both P2O5 and B2O3 enhanced the crystallization trend of rod-shape rutile and suppressed the crystallization trend of dendrite CaTiO3. Therefore the added P2O5 and B2O3 caused the primary phase change from CaTiO3 to rutile. Additionally, it was found that the rod-shape rutile showed a 1-D growth, whereas the dendrite CaTiO3 showed a 3-D growth style.

Jan 1, 2015

By R. W. Bartlett

The extensive central Idaho black sand placer deposits are a potential source of rare earth elements, particularly the heavy rare earth elements that are not prevalent in commercial bastnasite deposits. These placers derive from the Idaho batholith. The geology, occurrence, and extent of these deposits are reviewed and the diverse mineral assemblages and complex mineral chemical compositions of these sands are described. Niobium, yttrium and thorium are also present in significant concentrations. The results of prior mining practice, including concentration and separation of the heavy minerals are reviewed. Technical approaches to extraction of rare earths from Idaho black sand concentrates are discussed.

Jan 1, 1992

By Cynthia K. Belt

Improved energy efficiency has grown in importance within industry as energy costs have escalated. The analysis of trends and changes to a process is critical in making the best business decision in energy management. Frequently, energy use per day (Kilowatt-Hour or British Thermal Units) is used to track energy efficiency. Sometimes, the somewhat more complex method of energy per processed weight (Kilowatt-Hour per Metric Ton or BTU per Pound) is used to make this evaluation. Yet both methods ignore the effects due to throughput and weather. In this paper, different thermal processes and systems will be evaluated using statistical methods to highlight alternative methods to evaluate energy efficiency. Examples and potential problems will be discussed for both a single process and a collection of processes within a plant or corporation.

Jan 1, 2008

By F. Robert Hubbard

IMCO Recycling Inc. has developed a new, patented technology for the production of fertilizer, K-SOIL?, as a by-product of its aluminum recycling operations. This new technology can substitute for conventional technology which now results in a saltcake residue that is placed in 'landfills. Four years of research and development work by IMCO culminated in a U. S. patent issued April 5, 1994. As part of the technology development effort, IMCO engaged the services of a nationally renowned research organization and a prominent university. These two organizations have conducted in-depth agronomy studies In the laboratory, greenhouse, and the field. Results have shown K-SOIL? to be performance equivalent, on a nutrient content basis, to conventional potash fertilizer. The first field applications on commercial farms were made in the spring of 1994. K-SOIL? is a potassium-bearIng, granular solid which may find use in fertilizer blends, direct application, and other forms of fertilizer products. The overall benefit of this new technology is to create a useful by-product rather than generate a useless residue and, thereby, reduce or eliminate the amount of salt cake now placed in landfills. As such, It is a significant, step toward IMCO's ultimate goal of complete recycle.

Jan 1, 1995

By Lingling Zhang, Daqiang Cang, Guizhou Zhao

Pilot trial ofthe detoxification ofchromium slag in cyclonefurnace and the preparation of glass-ceramics were investigated in a power plant in China. 10wt.%chromiumslagweremixedwithpulverizedbituminouscoalandlimestone as the raw materials of the cyclone furnace. Cr(VI) in chromium slag was reduced toCr O insidethecyclonefurnace.Themeltwaswater-quenchedintofritandthen 2 3 fired into glass-ceramics with a laboratory ceramicrollerkiln. The preparation and crystallization behavior of glass-ceramics were investigated with differential ther- mal analysis (DTA), physical and mechanical properties testing, X-ray diffraction (XRD) and scanning electron microscopy (SEM). The optimal flexural strength exceeding 90 MPa were achieved in firing temperature zone of 1170–1200 °C. Anorthite (CaAl Si O ) and diopside [Ca(Mg, Fe)Si O ] can be identified in the 2 2 8 2 6 glass-ceramicsandCaAl Si O isthepredominantcrystalphase.Fineparticleswith 2 2 8 average diameter of 200 nm distributed uniformly in the glass-ceramics. Granular crystals are intensively interconnected and constituted a crystal skeleton soaked in theglassmatrix.LeachingtoxicitytestdetectedCr(VI)of0.016and0.010 mg/Lof the water-quenched frit and glass-ceramics, respectively. This method provides an effective and comprehensive technique for the detoxification and utilization of chromium slag at low cost and large-scale. (cid:1) (cid:1)

Mar 1, 2018

By M. Hochenhofer

Keywords: desulfurization, mathematical model, slag reaction To produce ferroalloys like ferro-nickel for alloying purposes in a quality that meets the requirements of today?s steel industry, refining processes like desulfurization and dephosphorization are indispensable. The performance of desulfurization-treatment by slag reaction depends on various parameters, such as: sulfide capacity and viscosity of the slag, sulfur distribution between metal and slag, activity of sulfur in melt and movement of melt. Within this work, the combined influences of these parameters on the desulfurization of a ferro-nickel alloy were examined. As a basis for this examination, a mathematical model, based on data from plant trials, was created. This model demonstrates the relationship between desulfurization rate and initial values of the above mentioned parameters. With this model the relevant parameters were evaluated and assessed concerning their influence on desulfurization.

Jan 1, 2005

By Eric J. Beckman

Recovery of metals from dilute solution, whether the matrix is solid, or liquid, remains a considerable technical and financial challenge. Methods currently exist whereby metals can be extracted from either type of matrix, yet these methods consume significant quantities of reagents and can also generate multiple waste ,streams in the process. Technology developed in our lab allows efficient application of environmentally-benign CO2 to a number of separation problems involving metals. For example, we have employed biphasic mixtures of C02 and water as a green acid leach medium. Metals have been extracted from a steelmaking process residue and then recovered as metal carbonates through depressurization. In this process, metals are extracted and recovered without the use of reagents other than CO2 and water, and CO2 is sequestered as a solid. In addition, through synthesis of Cal-miscible phase transfer agents, we have shown that CO2 can replace the organic solvent currently used in refining of precious metals, The sensitivity to pressure of phase behavior in a CO2-mixture may allow significant streamlining of the process as well. Finally, CO2 soluble chelating agents have been used to extract toxic metals from acidic effluent such as that found in plating facilities.

Jan 1, 1999

By Shuqiang Guo, Gonghui Yang, Xingxing Zhang, Yuyang Bian, Song Chen, Weizhong Ding, Yinhe Liu, Lan Jiang

One of the most promising refractory materials for application is zirconia in melting superalloy. In this work, the properties and phase composition of magnesia partially stabilized zirconia ceramics (MgO-PSZ) under different sintering temperatures were systematically investigated. Commercial magnesia partially stabilized zirconia (MgO-PSZ) powders were selected as the starting materials. The magnesia partially stabilized zirconia phase composition was measured by X-ray diffraction (XRD), the density of sintered samples was tested by vacuum density instrument, the thermal expansion were obtained by thermal dilatometer from ambient temperature up to 1450°C, and the microstructures of MgO-PSZ were characterised by scanning electron microscope (SEM). The results indicated that the properties of thermal expansion, densification, microstructures and phase composition were significantly affected by sintering temperature. Densification was consistent with SEM micrographs of MgO-PSZ at different sintering temperatures.

Jan 1, 2015

By Antonio Martin, Jesus Hurtado, Francisco Jimenez

"Atlantic Copper is one of the largest copper producers in Europe. Its production facilities, including a primary copper smelter and an electrolytic refinery, are located in Huelva, on the southwest coast of Spain. These installations enable the smelting of over 1 million tpy concentrates to produce up to 260,000 tons per year of cathodes and 900 ktpy of sulphuric acid.Since 1970, several improvements have been made at the Converters Area such as modifications of primary hoods, operations with an OPC system, installation of scrap chargers, the recent installation of the secondary hoods and other environmental projects. All these modifications have been aimed at increasing the capacity of our smelter while keeping our continuous environmental commitment.This paper describes the modifications and improvements carried out at the converters area and our proposals for future developments."

Jan 1, 2012

By J. H. Meza

La Caridad copper smelter is located in the magnificent but rugged Sierra Madre Mountains. This project presents unusual challenges that require the utmost in detailed analysis and planning. The smelter, owned by Mexicana de Cobre, S.A. de C.V., has an annual production capacity of 225,000 metric tons of copper and 600,000 metric tons of sulfuric acid. It utilizes only the Flash Smelting process. This project will expand the annual production capacity to 270,000 metric tons of copper and 1,000,000 metric tons of sulfuric acid. Offgases from the Flash Furnace and the Teniente Converter will be sent to a mixing chamber, from which it will be led to two sulfuric acid plants. This project will then produce a high quality sulfuric acid.

Jan 1, 1995

By J. L. Delplancke

During copper electrowinning in sulphate electrolyte, intense oxygen evolution takes place at the anode. Lead alloy anodes are progressively replaced by dimensionally stable anodes in order to avoid the cathode contamination by dissolved lead. The electroactive coating of these anodes has to be as cheap as possible, adherent to the substrate, electrochemically stable and has to be efficient at high current density and high temperature. This requirement is even demanding in case of copper electrodeposition for the production of thin copper foils for the electronic industry. The production of thin (20 µm thick) copper foils for the printed circuit boards requires high purity copper electrodeposited at a current density as high as 7,000 A/m2. The choice of a long term coating composition is driven by economics. The purpose of this paper is mainly to review the anode compositions suitable for copper electrowinning and for copper electrodeposition at high current density. A short description of preliminary results obtained with a new anode coating on a titanium substrate is also presented.

Jan 1, 1999

By Maryam Ghodrat, Bijan Samali

Treatment of polymer-based wastes has a tremendous potential for generating alternative energy, reducing greenhouse gas emissions, creating economic and environmental benefits, and achieving a sustainable development of the energy sector. During the past few decades, plastic waste generation increased at a greater rate than the population, with the move towards single-use products. Also with raising the cost of oil-based products, greater emphasis should be placed upon the usage of plastic/polymer in the waste stream as a supplementary source of fuel. This study presents a techno-economic analysis of the recycling potential of plastic waste in Australia by evaluating the possible use of these wastes as a reductant in steel making incinerators. The study tries to shed light on a possible cost effective alternative route in the smart treatment of waste plastic in Australia.

Mar 1, 2018

Many studies have been conducted over the past 3 decades on the leaching of gold in solutions containing thiosulfate, ammonia and copper. However, most of these studies have been carried out using ore samples, with very few fundamental studies of this system being attempted. The majority of the published studies have failed to acknowledge the undesirable side reaction between copper(H) and thiosulfate, let alone account for its effect. The fact that the solution chemistry is constantly changing makes it very difficult to perform a fundamental study of gold leaching. With the advent of the rotating electrochemical quartz crystal microbalance (REQCM), such fundamental studies are possible as this instrument measures mass in real time. This has allowed leach kinetics to be measured in a matter of minutes and hence at essentially constant solution conditions; The present paper highlights that a sufficient concentration of copper(II) and ammonia are required in order to achieve appreciable gold leach rates. However, the use of air (oxygen) to maintain the copper(Il) concentration catalyses the undesirable copper(II) reaction with thiosulfate. The presence of ammonium ions is shown to have an effect on this undesirable reaction as well as on the gold leaching ?reaction. Preliminary electrochemical studies into .gold electrowinning using the REQCM show that gold(I) thiosulfate cannot be readily reduced to metallic gold in the potential region at which cementation usually occurs. However, it is well known that gold cementation onto copper occurs rapidly. The current study addresses this discrepancy by studying the effect that copper and silver have on the reduction of gold thiosulfate. It has been found that the presence of both silver and copper enhance gold deposition, particularly at low over potentials. While this is beneficial in cementation, the presence of copper and silver in solution has been found to cause passivation of the cathode surface during electrowinning at 'higher overpotentials.

Jan 1, 1998