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By I. A. Ibrahim

Ilmenite, in its natural form, is an inactive mineral from which the selective removal of iron is rather difficult. The reactivity of ilmenite. so that it can be leached with dilute hydrochloric acid, can be enhanced by chemical reduction in solution using a suitable metal as a reducing agent. The present paper aims at the evaluation of an Egyptian ilmenite ore for the production of synthetic rutile by direct leaching with hydrochloric acid in presence of iron powder. In this process, the titanium and iron contents are dissolved; meanwhile, the dissolved titanium is hydrolyzed and re-precipitated leaving mainly iron in solution. Leaching conditions were optimized to obtain less iron in the final solid product. Addition of sufficient amount of iron powder during leaching reduces the dissolved Fe3+ to Fe2+ and reduces the dissolved Ti4+ to Ti3+. The creation of Ti3+ in solution is assumed to have a role in dissolving the ferric iron and hence increasing the reactivity of the ilmenite ore. Synthetic rutile of about 90% TiO2 and 0.77% Fe2O3 was obtained from ore with a grain size 100% passing 200 mesh and a 5-hour leach time with 20% HCl at boiling temperature (110°C) and 0.11 g iron powder / g ore.

Jan 1, 2003

By W. G. Davenport

Chapter 6 examined autotherrnal smelting of pure chalcopyrite concentrate with 50 mass% O2-50 mass% N2 blast. It showed that production of 1500 K products with this blast requires: 181 kg of pure oxygen 337 kg of air per tonne, of concentrate. It also showed that the grade of matte produced with this blast is 58% Cu. This chapter re-examines autotherrnal smelting by asking: (A) WHAT COMPOSITION BLAST (MASS% 02 -MASS% N2), 298 K, WILL AUTOTHERMALL Y PRODUCE 65% Cu MATTE 1500 K FROM PURE CHALCOPYRITE CONCENTRATE? (B) HOW MUCH PURE OXYGEN AND AIR WILL BE NEEDED? These are important questions for flash? smelting because furnace operators usually want to send specific composition matte to converting. This chapter shows how a specified matte can be produced autotherrnally with 298 K oxygen-air blast. Later chapters show how it can be done with hot blast, hydrocarbon combustion, different concentrates etc.

Jan 1, 2001

By Shigehito Isobe

The Li-N-H system composed of LiH and LiNH2 catalyzed by titanium compound desorbs ~6 mass% hydrogen and a quite small amount of ammonia in temperature range from 150 to 250 °C under He flow atmosphere. In this work, hydrogen desorption (H-desorption) mechanism in the reaction from LiH+LiNH2 to Li2NH+H2 in a non-equilibrium condition was clarified by TDMS, TG and FT-IR analyses for the products replaced by LiD or LiND2 for LiH or LiNH2,respectively. The results suggested that H-desorption reaction progresses through two-step elementary reactions mediated by ammonia. As a next step, we carefully determined the amount of the ammonia containing in desorbed hydrogen for the Li-N-H system in a closed system from the practical point of view. The results indicated that a quite small of ammonia thermodynamically coexisted in the desorbed hydrogen in closed system, although ammonia could not be almost detected in emitted hydrogen gas by TDMS under some non-equilibrium conditions. Moreover, for understanding the role of titanium, the chemical bonding state of the titanium compounds doped as catalyst in the mixture was examined by XAFS measurement. The results indicate that the Ti atoms, which can induce catalytic effect, are in a particular chemical bonding state.

Jan 1, 2006

By Paul B. Queneau

U.S. plants solely devoted to recovering values from metal-rich wastes have established market niches based on one or more competitive advantages: superior process technology, access to key feedstocks, unique equipment, special knowledge of markets, and an appropriate exit for outfall water. Plant methodology, competitiveness, environmental factors, and economics are examined, with particular attention to feedstocks, technologies, products, and outputs.

Jan 1, 2003

By Hongbo Zhu, Kun Yang, Jingyan Jia, Jinhui Peng, Libo Zhang, Yi Xia

"Titanium dioxide is broadly considered as the most potential useful photocatalytic material. In this work, titanium dioxide was synthetized by microwave solid-state method and characterized by thermogravimetry-differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The result demonstrates that through microwave solid-state synthesis, we can obtain uniform size and anatase TiO2 photocatalyst, with the precursor being Ti(C2O4)2·2H2O. And its degradation kinetic parameter of MO can reach to 0.21232.IntroductionSince Fujishima and Honda found the photovoltaic property of titanium dioxide TiO2 [l], it has been widely used in the field of pollutant degradation, virus killer and environment protection [2-5]. Compared to other semiconductors, TiO2 has the advantage of low toxicity/cost, chemical stability, excellent photocatalytic activity, and long lifetime of electron/hole pairs, thus it is considered to be a most potential useful photocatalyst material [ 6]. Solid-state synthesis of oxide nanoparticle is a new method developed in recent years, which not only overcomes the shortcomings of easily aggregation existing in traditional hydrometallurgical process, but also fully demonstrates the unique technologic advantages of without solvents, high yield, easy control, less environmental pollution in solid-state reaction [7-11]. Researches show that the new method of microwave synthesis shows a lot of advantages such as fast reaction rate, efficient, high purity of product, uniform morphology, energy-efficient, and nonpolluting [12-15].In this work, we associated microwave heating and solid-state synthesis to prepare TiO2 photocatalyst material. Its photocatalytic activity was studied in the degradation of MO queous solution. Meanwhile, the formation process as well as the crystal structure and morphology of the synthesized powders were characterized by means of chermogravimetrydifferential scanning calorimetry (TG-DSC), X-ray diffractometry (XRD) and scanning electron microscopy (SEM) techniques."

Jan 1, 2014

By Alireza Zakeri

To evaluate the behavior of minor elements in the copper smelting process, activities of silver, selenium and tellurium at minor concentration were determined at 1473 K within the miscibility gap of the Cu-S-Me (Me = Ag, Se, Te) and Cu-Fe-S-Me systems varied in Fe/Cu ratio. Phase relations between the immiscible metal and matte phases in the foregoing systems were first established by a quenching technique at 1473 K to supplement the activity measurement data. A Knudsen-effusion mass spectrometer, capable of handling complex gaseous systems and relatively small vapor pressures, was adopted for activity determination. Using a multiple Knudsen-cell, the ion intensity of minor element in the sample under study was measured simultaneously with that in a reference sample. Activity was obtained from the ratio between the measured ion intensities as well as the known activity value of the minor element in the reference sample. Limiting activity coefficients of the minor elements were correlated with composition of the matte. Based on the experimental results, the vaporization behavior of the minor elements has been discussed.

Jan 1, 1999

By Larry Southwick

In the early 1940's, the Caron ammonia ? ammonia carbonate leach process was used to produce nickel from Mayari ores at the Nicaro plant in Oriente Province, Cuba. While plant operation was generally successful, it was not broadly economical and was shut down. The plant was later restarted in the 1950's and a number of investigations initiated to resolve the more serious operational and performance issues. Processing steps studied included iron reduction (chemistry ? nickel and iron, reductant, equipment), ore variability (homogeneity and consistency of mineral concentrations, serpentine vs. laterite), leach solution strength, nickel recovery (temperature ? reduction and leaching, reoxidation) and a variety of other topics. These studies and their findings will be discussed. Caron himself obtained good results on these ores in the laboratory. They could not be duplicated in the field, the reasons for which will be reviewed. (Note: the ore looked like garden dirt; charcoal made from palm trees was one of the reductants attempted; and ammonia was the leach solution. Mixing the three, so to speak, was to yield nickel.)

Jan 1, 2006

By Florian Kongoli

The optimal operation of the blast furnace depends considerably on the properties of the sinter fed into the furnace. As a result, the optimization of the sintering processes has a direct effect on the overall effectiveness of the iron making processes. In order to produce a good sinter special care needs to be taken in order to assure it has a good permeability and reducibility and it is able to retain these properties for a certain time. If the sinter starts to melt down early in the upper part of the blast furnace, where its solid state reduction is essential, permeability decreases, the gas channels get blocked, reductibility diminishes and serious problems may also follow. Among the factors that influences the above mentioned sinter properties are the oxygen potential and fluxing components. Nevertheless, their effect on the phase relations during sintering and sinter reduction conditions has not yet entirely clarified and confusion exists in literature. This quantification becomes even more important today where many new minor components such as Al2O3 and MgO enter the sinter through raw materials. This work quantifies the effect of oxygen potential and fluxing components such as alumina and magnesia on the liquidus and phase relations of the sinter primary melts in the iron rich portion of CaO-FeO-Fe2O3-SiO2 system at sintering conditions. This is carried out by the means of new type of industrial diagrams in the form of Fe/CaO vs. SiO2 that can directly help the optimization of the sintering processes.

Jan 1, 2006

By Jun Li

Several metal sulfides were examined in-situ by Raman spectroscopy before and after anodic oxidation. Results obtained for chalcocite, chalcopyrite, covellite, galena, pyrrhotite and pyrite electrodes are presented. Under appropriate conditions, sulfur was detected after a potential was applied to the mineral electrodes for a threshold period of time. For all the minerals, application of a negative potential on the oxidized mineral reduced the surface product and the sulfur peaks disappeared from the observed spectra. For those minerals containing sulfur as S< in the crystal lattice, polysulfides were identified as oxidation intennediates.

Jan 1, 1993

By Jiang Diao, Yong Qiao, Xuan Liu, Tao Zhang, Bing Xie

The equilibrium experiments between the FeO-SiO2-MnO-TiO2-V2O3-Cr2O3-MgO slag system and solid pure iron were performed to investigate the vanadium and chromium distribution ratio under Ar atmosphere. The influence of w(FeO), w(V2O3) and w(Cr2O3) in slag on vanadium and chromium distribution ratios were studied at 1653 K. The experimental results were compared with calculated distribution ratios based on molecule and ions coexistence theory. Both of them showed that higher FeO content in slag would improve the distribution ratios of V and Cr between slag and hot metal. The distribution ratio of Cr or V increased with the increase of Cr2O3 or V2O3 content, respectively. To optimize the oxidation of V and Cr from hot metal, a high oxidizing slag and suitable content of Cr2O3 and V2O3 in the slag were recommended. The results provided reference for the further study on the extraction of V and Cr in VTi magnetite.

Jan 1, 2016

By Carole Read

Hydrogen is under consideration by several countries for its potential as an energy carrier for transportation applications. In order to compete with vehicles in use today, hydrogen-powered vehicles will require a driving range of greater than 300-miles in order to meet customer needs and expectations. For the overall vehicular light-duty fleet, this dictates that a range of 5 to 13 kg of hydrogen be stored on-board (assuming a fuel cell power plant) within stringent system weight, volume, and cost constraints. Vehicular hydrogen storage thus constitutes a major scientific and technological challenge. To meet this challenge, the U.S. Department of Energy (DOE) initiated a ?National Hydrogen Storage Project? with roughly 40 universities, 15 companies and 10 federal laboratories, actively engaged in hydrogen storage research. Centers of Excellence in metal hydrides, chemical hydrides, and carbon-based materials have been established, as well as independent university and industry projects in the areas of new concepts/materials, hydrogen storage testing, and storage system analysis. Recent technical progress in each of these areas is discussed, as well as collaborative hydrogen storage activities under the recently established International Partnership for the Hydrogen Economy (IPHE).

Jan 1, 2006

By Guozhu Ye

Hydrometallurgical zinc recovery from EAF dust has several advantages compared to pyrometallurgical alternatives in terms of low temperature operation, lower energy consumption and higher flexibility. Many hydrometallurgical processes have been suggested and tested over the years without success. The main reasons are: -Low leaching yield of zinc due to the fact that a high fraction of ZnO in the EAF dust exists in the zinc ferrite structure which makes selective leaching of ZnO not possible -Many of the proposals could not handle the halide in the EAF dust To eliminate these two disadvantages, two zinc ferrite elimination concepts have been tested and developed in the REZIN project of the EU 5th Framework Programme. The two concepts for zinc ferrite elimination could be shortly described by the following chemical reactions: A. ZnOFe2O3 + 2CaO = Ca2Fe2O5 + ZnOfree B. ZnOFe2O3 + C = Femet + CO/CO2 + ZnOfree These two concepts were investigated in details in combination with a subsequent leaching step using the novel EZINC process for recovery of zinc from EAF dust. Leaching of pretreated samples has shown great increases of a zinc recovery yield. A zinc recovery of over 90 % could be reached, as compared to about 50 % for no-pretreated samples. This paper will describe the two concepts in details.

Jan 1, 2006

By Frustino L. Prado

For more than a century, the AAC (ammonia I ammonium carbonate) process has been applied to the recovery of various metals. A variation of it, the Caron Process was first used in the early 1940&apos;s in Cuba for the extraction and recovery of nickel from laterites. The original Nicaro plant has been in continuous operation since then. Years later the Caron process was used again in Australia at the Greenvale (Yabulu) NickelICobalt plant, commissioned in 1974. Other projects (Sered, Niquelandia, Nonoc, Punta Gorda, Albania) as well as several studies have been carried out. The Caron Process is alive and still promising. Members of our organization have been working with AAC and the Caron Process since 1952. This paper will review current approaches and potential improvements (enhancement of recoveries of Ni and Co, reduced energy consumption and maintenance simplification). Keywords: Caron Process, Ammonia, Ammonium Carbonate, Laterites, Nickel, Cobalt

Jan 1, 2004

By Florian Kongoli

The liquidus surface of multicomponent slags is an important parameter in various smelting and converting processes. It helps not only to optimize the slag, chemistry of current processes and their fluxing strategies, but also to determine the availability of new slags for more advanced technologies. In a series of our previous publications, the liquidus surface of some multicomponent iron oxide slags has been quantified at several constant oxygen potentials and the effect of the latter, ignored until that moment, was quantified along with the effect of some minor components. In this work, the liquidus surface of some iron oxide slags is quantified at constant CO2/CO ratios. This is a new convenient way for the quantitative description of the slag liquidus surface and the effect of several fluxes, especially in those processes such as slag solidification, where oxygen potential changes continuously. This type of diagram also describes more dynamically the effect of oxygen potential, clarifies the relation between CO2/CO ratio and oxygen potential in terms of the liquidus surface, which is not widely understood by metallurgist today, and reduces the gap between laboratory work and industrial experience.

Jan 1, 2002

By Kwang-Ho Lee

The Onsan copper smelter of LS-Nikko Copper Inc. has operated the Mitsubishi continuous process along with Outokumpu process since 1997. Mitsubishi process is a bath smelting process which needs adequate melts for smelting reaction in the furnace. After a campaign shutdown it requires time to make a start melt. Onsan smelter has had much experience in flash smelting, including the improvement of the concentrate burner which is one of the most important parts in a flash smelting furnace. Based on this experience, the lances of the Mitsubishi smelting furnace were modified in order to making the starter melt with flash reaction. In 2004, the flash reaction in the Mitsubishi S-furnace was completed and was able to make the starter melt using these modified lances. Although at that time it was still under development it reduced the time required to make the initial bath-melt by about half.

Jan 1, 2006

By Bradford C. Wesstrom, Omar Araujo

"Impurities from an electrolytic refinery are typically extracted from the electrolyte utilizing conventional electrowinning cells. These cells are arranged in series with cascading solution flow and are commonly referred to as liberator cells. The Freeport McMoRan Copper & Gold El Paso Refinery has optimized the removal of arsenic in cascading liberator cells by utilizing two separate feed solutions. The primary feed solution is recycled liberator electrolyte and the secondary feed solution is ""neat"" tank house electrolyte. The secondary feed solution is added based on the voltage response across the individual cells utilizing independent variable frequency drive (VFD) pumps. When the voltage across a cell changes, a signal is sent to the VFD pump to maintain a cell voltage of 1.98 volts. By maintaining this voltage the copper content in each cell exits at 2-4 grams per liter. This safely optimizes the arsenic removal as copper arsenides on the liberator cathodes.IntroductionDuring the electrolytic refining of copper, impurities from the copper anode report both to the bottom of the electrolytic refining cell as slimes and to the electrolyte. The impurities which enter the electrolyte are arsenic, antimony, bismuth and nickel. The impurities that report to the electrolyte during the electrolysis process gradually increase. As these impurities increase, they are incorporated into the refined copper cathode. There are many processes that have been used to remove these impurities from refinery electrolytes. Some of them are listed as follows: solvent extraction, ion exchange, hydrogen sulfide reduction, bioreactor, adsorption onto a low - solubility metal-oxide hydrate, adsorption onto activated carbon and EMEW cells. The conventional process used by the copper refining industry for controlling the level of impurities in electrolyte involves multistage electrolytic cascading liberator cells. In these cascading liberator cells copper, arsenic, antimony and bismuth are removed as various mixed deposits from the electrolyte. Removal of these impurities is achieved through an increase in voltage resulting from the depletion of copper in the electrolyte through electrowinning. With this higher voltage, the Group Vb elements, arsenic, antimony and bismuth are deposited on the copper cathode and report as slimes to the bottom of the cells. Nickel is removed in a subsequent process."

Jan 1, 2012

By John O. Marsden

In early 1998, Phelps Dodge embarked upon a program to investigate alternative technology for the extraction and recovery of copper, and other metal values, from copper concentrates. A review of all of the available process alternatives indicated that many were unsuitable for large-scale commercial application and others were clearly targeted at niche applications where contaminants (and consequently smelter penalties) were driving the decision-making. The result of this development program is the world?s first commercial application of high temperature pressure leaching of chalcopyrite concentrate at Bagdad, Arizona, which was commissioned in the second quarter of 2003. Other related processes are in various stages of development. In addition to the obvious considerations, the economic aspects of this technology have been considered in detail at each step in the development of the program. The technology developments in this area are reviewed with emphasis on the economic viability and commercial application.

Jan 1, 2003

By Wenbo Luo, Kang Liu, Fusheng Mao, Jilai Xue, Jun Zhu, Chunlei Yang

Extracting alumina from coal fly ash (CFA) is of great interest for both environmental protection and recycling valuable alumina content. In this study, ultrasonic aided leaching process as an effective method was investigated to enhance extracting Al2O3 from CFA via concentrated sulfuric acid sintering. The influence of ultrasonic power and processing time were tested under the conditions as the same as those without ultrasound. It is found that the alumina extraction rate can reach 90.5 % with ultrasound assistance, while the ultrasonic treatment can reduce almost 15 ~ 30 min in leaching time and 5 ~ 10 oC in leaching temperature than those without ultrasonic operation at the same Al2O3 extraction rate. In addition, the ultrasonic can reduce calcium content by 6 ~ 8 % dissolved into the leaching liquid. SEM analysis also shows that the residue particle size with ultrasound is smaller than that without ultrasonic treatment.

Jan 1, 2015

By Gary Kordosky

Equilibrium modifiers, first introduced into copper solvent extraction reagents in the late 1960?s, are widely used. The properties of various equilibrium modifiers with respect to copper extraction, selectivity, reagent stability and entrainment are discussed and some conclusions are drawn relating the structure of the modifier to the properties of the modifier. A new highly selective, low viscosity modifier is also introduced.

Jan 1, 2003

By Jitka Jandová

A laboratory process based on simple and environmental friendly operation, aimed at recycling of spent Li/MnO2 batteries, is described in this study. This process involves roasting Li/MnO2 batteries in a vacuum furnace at 650°C, followed by selective leaching Li2CO3 from calcined electrode material in distilled water at ambient temperature and controlled crystallization of pure Li2CO3.

Jan 1, 2006