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By Corby Anderson

The efficient separation of palladium from the transition metals copper, nickel and iron can be effected by passing a leach solution of these metals through a column of the silica polyamine composite material, WP-1, patented by Purity Systems Inc (PSI), Assignee, University of Montana with exclusive license to PSI. The separation can be done at the intrinsic pH of a nitrogen species catalyzed (NSC) oxidative pressure leach solution (~0) and stripping of the palladium from the composite can be effected with hydrochloric acid/ammonium chloride solutions at 50oC. Batch capacities of the composite for palladium are ~ 1.8 mmol/g resin. The possibilities for isolating the metal from the strip are discussed. Given the proven longevity and rapid capture kinetics of the polyamine composites, this new approach should prove to be an economically viable alternative to the multi-step concentration processes practiced in the PGM industry to date.

Jan 1, 2003

By Chang-hong Peng

Solubility phase equilibrium in the ternary system of Me2+-NH4+-SO42--H2O (Me2+ represented Mn2+, Zn2+ and Fe2+) was studied by the isothermal method at 298K and physicochemical properties of the saturated solution such as density, refractive index and pH were also investigated. The experimental results show that the solubility isothermal phase diagrams of these systems consist of three invariant branches, two invariant points and three crystallization fields. Corresponding to the three crystallization fields, there have three phases of solid, that is MeSO4?nH2O, (NH4)2SO4 and (NH4)2Me(SO4)2?6H2O, respectively. At the eutectic point, the concentration and the refractive indexes of the saturated solution change evidently. Otherwise, the pH value change slowly in all the systems. The calculated results of the density and refractive index agree with the experimental results.

Jan 1, 2006

By Guo Xueyi

The reaction mechanism for the manganese dioxide reductive dissolution in acidic chloride media in the presence of ferrous/ferric ions are based on theoretical delineation and dual cell experiments. In terms of the Buttler-Volmer equation and chemical kinetic principles, a electrochemical kinetic equation was deduced, which successfully provided a theoretical basis for describing the role of Cl-, Fe2+, Fe3+ and H+ in solution, as well as their interrelationship in manganese dioxide reductive dissolution. Dual cell experimental studies indicate that the increases of Cl- and Fe2 in solution are helpful to accelerate the couple process; while, Fe3and Mn2+ hinder the coupled reaction to some degree. Higher acidity in solution is beneficial to the dissolution of MnO2. All the dual cell experimental results are consistent with the theoretical deduction. This study will be useful to understand the mechanism for the leaching of manganese nodules from the deep ocean, as well as the leaching of manganese dioxide ore from land.

Jan 1, 2003

By Kaspar Tall, Dmitri Goljandin, Kristiina Vilsaar, Jaan Kers, Valdek Mikli, Lifeng Zhang, Riho Tarbe, Viktor Laurmaa, Mart Saarna, Priidu Peetsalu

In this paper, the mechanical milling of the Printed Circuit Boards (PCB) was carried out. First goal of the work was to examine the management of the WEEE, in particular the re-use of PCB. Firstly, recycling methods of PCBs were summarized. During the study mechanical separation methods (magnetic-, density- and air separaten), electrical, and chemical methods were examined. Secondly the optimal particle size for air-classification was determined. Several tests were carried out to find the most effective separation method for separation of different material groups from PCB scrap. The new air classification stand was developed for testing the separation of lightweight particles like tinfoil stripes and plastics. The test results showed sufficiently good separation of heavier Al and Cu. For milled materials characterization the SA, IA, laser diffraction analysis and SEM were used. The chemical composition of the PCB powders was studied by means of energy dispersive X-ray microanalysis (EDS).

Jan 1, 2011

By Sundarrajm Suresh, Hrushikesh G. Pimpalgaonkar, Thiyagarajan Paramadayalan

In this paper, a model of a fuel cell system has been proposed to account for the membrane physics at the micro level which is coupled with the macroscopic flow and mass transport phenomena occurring in a single channel of a Polymer Electrode Membrane Fuel Cell (PEMFC) system. We have developed a novel approach to model the catalyst layer electrochemical processes in a Membrane Electrode Assembly (MEA) and coupled it with mass transport and fluid flow calculations at the channel level using STAR-CD commercial software. The predicted values of the cell voltage from this micro-macro model are validated with experimental data available in the literature. A sensitivity analysis has been carried out to study the effect of the design and operating parameters such as catalyst loading and initial temperature on the overall performance of the PEMFC. The results indicate that the cell voltage increases at higher platinum catalyst loading and is also independent of the choice of initial cell temperature.

Jan 1, 2012

By A. K. Kyllo

The use of Composite Furnace Module cooling systems has been shown to give improved refractory performance in a number of above bath locations in WMC flash furnaces. To test the behaviour of modules in contact with a melt, a set of instrumented modules have been installed in the reaction shaft of a. nickel flash furnace. The location was chosen to provide a suitably harsh environment to ensure rigorous testing, while still allowing relatively easy access for module installation. The modules were continuously monitored to provide information on the module performance, as well as the temperature in the shaft itself. The shaft temperature showed significant transient behaviour, which resulted in heat fluxes through the modules ranging from 10 to 92 kW m-2. The modules were capable of handling the highest heat flux with no risk of the coolant boiling. This paper details the design and operation of the modules over a period of seven weeks.

Jan 1, 1999

By J. L. Bill

The capacity of the Mount Isa Mimes Limited Copper Smelter was expanded in 1998 from 180,000 tomes per year of anode copper to 265,000 tpy. It is based on the innovative Copper ISASMELT technology, which currently treats concentrate at up to 184 tph. Increasing lance-air oxygen enrichment increased the ISASMELT furnace feed rate from 102 to 184 tph. The increased feed rate was achieved without any modifications to the ISASMELT furnace. The first refractory campaign following the upgrade lasted for two years. Future campaign lives of four years or more--without water cooling-are possible. Other Copper ISASMELT furnaces are operating in the U.S.A., Belgium, and India, with additional smelters under construction in China and Germany. In addition, Lead ISASMELT furnaces are operating in the U.K. and Malaysia. The paper discusses the performance of the MIM Copper ISASMELT furnace and the Copper Smelter since the expansion, including operating data and refractory performance.

Jan 1, 2002

By Broggi Andrea

Condensates produced by SiO(g) and CO(g) have a crucial importance in silicon production. Condensation will follow the reactions 3 SiOðgÞ+COðgÞ→ 2 SiO2 + SiC and 2 SiO ðgÞ→Si+SiO2. Solid compounds generated during silicon production contain Si, SiO2 and SiC in different microstructures and amounts. In industrial systems, condensates limit the SiO(g) escape to the off-gas system. On the other hand, they can block the gas flowing from the high temperature zone, hence the necessity of studying an optimized condensation process. This review discusses SiO(g) condensation and its interaction with CO(g). The report gives an overview of the condensates found both at laboratory and at industrial scale. The two main compounds are the Si–SiO2 and the SiOx–SiC mixtures. The hypothesis on the mechanism of formation of SiC–SiOx condensates is presented through a wide selection of performed works. The advantages and disadvantages of the former experimental procedures are discussed.

By Andrea R. Kim, Ramana G. Reddy

Electrodeposition of cobalt from cobalt chloride using the urea and the choline chloride ionic liquid (2:1 molar ratio) was studied to search the optimized parameters for the higher current efficiency. The cyclic voltammetry was tested with 0.2 MCoCl2 using various scan rates to determine the reduction potential in Urea/ChCl at 323 K. Based on the data from cyclic voltammetry test, the transfer coefficient and the diffusion coefficient were calculated as 0.22 and 3.38 × 10−6 cm2/s, respectively. The parameters for electrodeposition of cobalt were various temperatures (323 –383 K), applied potentials (2.4 –3.3 V), and concentration of CoCl2 (0.2–0.5 mol/L). Current efficiency and energy consumption were calculated to investigate the optimal condition for the electrodeposition of cobalt. The highest current efficiency (95%) was obtained under the temperature 323 K, the applied voltage 2.7 V, and concentration 0.5 mol/L of CoCl2. Scanning electron microscope (SEM) and X-ray diffraction (XRD) were used for the characterization of cobalt deposits.

Mar 1, 2017

By Theodore Ineich

The “BIOMOre” project aims to prove the technical feasibility of indirect in situ bioleaching of sulfide minerals contained in a deep underground deposit, by bringing together the disciplines required to make a success. The underground location in Poland was provided by project partner KGHM inside an operating copper mine. Key components of this project were the design and construction of a pilot plant, and its operation in an underground environment. This project also included a ∼250 t (100 m3) fragmented rock reactor hydraulically connected to the pilot plant. The pilot plant consisted of several tanks and pumps, a fluidised bed ferric iron generating bioreactor containing immobilised acidophilic iron oxidation biomass, and all the required instrumentation and utilities. Before the bioleaching phase could start, the rock reactor had to be flushed continuously firstly with water to remove chloride salts that are corrosive and also harmful for the bacteria used in the bioreactor, and secondly, with sulfuric acid solution to react with the carbonates present in the ore matrix. This paper summarizes the design, construction, commissioning, and operation of the pilot plant.

By Shangshu Li, Xin Li, Xionggang Lu, Xingli Zou, Kai Zheng, Yinshuai Wang

Ti5Si3/TiC composite has been successfully prepared from the titanium-rich slag/SiO2/C mixtures precursors by an electrochemical process. The electrochemical production process was carried out in molten CaCl2 salt at 1000 °C and 3.8 V. A pressed cylindrical pellet of titanium-rich slag/SiO2/C mixtures served as a cathode, and a solid oxide oxygen-ion-conducting membrane (SOM) tube filled with carbon-saturated liquid tin acted as an anode. The phase transformation of the cathode pellets during electrolysis process was investigated, the microstructure of the obtained products was characterized. It is found that the reaction pathways can be divided into three main stages during the electro-reduction process. The first stage is the generation of calcium compound, the second stage is the electrochemical reduction of the compound, and the third stage is the formation of Ti5Si3/TiC composite. The prepared Ti5Si3/TiC composite exhibits homogenous and nodular particle morphology.

Mar 1, 2018

By Rodríguez M. Esperanza

The efficient performance of Pachuca tanks is strongly linked to the suspension of mineral particles, which results from the motion of the liquid caused by injected gas rising, in general, through a central draft tube. This study reports a computational investigation on the effect of operating and design parameters on the suspension of particles. By extending the classical 2-phase drift-flux model to compute the gas hold-up, the three-phase (water-air-particles) system was simulated as consisting of a variable-density liquid plus the solid particles. These two phases were treated as interpenetrated continua using an Eulerian approach to set a turbulent recirculating flow model in 2-D and transient state. The model predicted adequately the measured critical superficial air velocity, uc, needed for maintaining particle suspensions, in pulps with 10-50 wt% solids. Additionally, the model was used to investigate the operation of industrial size reactors, obtaining results that agree well with the general trends reported in the literature, and highlighting important differences with respect to laboratory-scale reactors.

Jan 1, 2009

By Isadora Dias Perez, Denise C. Romano Espinosa, Flávia P. Cianga Silvas, Jorge A. Soares Tenório, Mónica M. Jiménez Correa

In view of the rising generation of wastewater containing metals, sustainable and clean techniques to recover them are being researched. This study investigated the adsorption of aluminum, cobalt, chromium, copper, iron (III), magnesium, manganese, nickel and zinc presents in a synthetic ef fluent by chelating ion exchange resin Dowex XUS43605. The resin was tested in columns experiments and was analyzed the flow rate (0.45, 0.66 and 1.11 BV/h), at pH 1.5 and 20 °C. After loading the column, the elution experiments occurred with 1 M of H2SO4 and 4 M of NH4O. The concentration of the metals in solution was obtained by X-ray fluorescence spectrometry energy dispersive (EDX). The results showed that the breakthrough experimental curves demonstrated that the main metals (aluminum, cobalt, manganese and zinc) were immediately broken through just after the initiation of the feeding, while the breakthrough of copper began later. Therefore, the study showed that the chelating resin could be used to treat contaminated effluents with metals.

Mar 1, 2017

By W. D. Cho

Fast dissolution of nonmetallic inclusions such as alumina particles in molten slags has been required in secondary steelmaking -ladle and tundish - to minimize the amount and the size of nonmetallic inclusions in steel products. In the present work, the dissolution behavior of alumina particles in molten CaO-A12O3 and CaO-A12O3-SiO2 slags at the temperatures between 1450 and 1550°C have been investigated in terms of kinetics and mechanism. Alumina particles were added directly into the slags and the variation of the particle size with time was determined using optical and electron microscopies. The conventional types of slag for ladle and tundish were included in the dissolution study. The effects of Al2O3, Siq, CaF2 and MgO contents on the dissolution rate of alumina particles have also been determined. The diffusion boundary layer between alumina particle and bulk slag phase has been observed and analyzed using SEM and EDS. Based on the analysis of kinetic data and the boundary layer, the dissolution mechanism has been discussed.

Jan 1, 2002

By James R. Craig

Petroleum coke is becoming an increasingly important source of light hydrocarbon products as product crudes become heavier and of poorer quality. The use of petroleum coke to generate synthesis gas results in the formation of residual slags that are enriched in silica, alumina, sulfides, oxides, and free metals. The characterization of these slags and their con? stituent phases is an essential step in considering the ultimate use or disposal of such slags and in understanding how to alter the properties of the slags to optimize the efficiency of gasifiers. Depending upon temperatures and bulk compositions, quenched slags typically consist of silicate glasses, calcium silicates, iron-nickel oxide-sulfide masses, aluminate spinels and free metals. Whereas the glasses contain relatively uniformly dispersed metals and sulfur, the iron-nickel oxide-sulfide masses highly concentrate nickel and sulfur. The aluminate spinels very effectively concentrate vanadium and chromium, thus depleting glasses or other adjacent phases. The abundance as well as the make up of the slags strongly affects the physical behavior of the slags within the gasifiers

Jan 1, 1989

By Jing Zhan

The fibrous precursor can be obtained by coordination precipitation process, using oxalate, cobalt chloride and ammonia. The composition and morphology of fibrous precursor were characterized by XRD, IR, DTA/TGA and SEM analysis. The results show that XRD pattern and composition of the precursor with fibrous morphology precipitated at pH=9.0 were different from that of ß-CoC2O4?2H2O precipitated at pH=1.0. The mechanism on the thermal decomposition of fibrous precursor was addressed. The influences of various conditions in pyrolysis, including the temperature, time, atmosphere, and the morphology of the precursor, on the morphology, average size and specific surface area of the Co powders were investigated in detailed. At last, the final product, fibrous cobalt powders with diameter about 0.3~0.5µm in size and 40~60 in aspect ratio, were produced by thermal decomposition at 400~500? in the weak reducing atmosphere. The structure of pores in cobalt powders was capillary tube with open ports and the majority was mesoporous.

Jan 1, 2009

By Alex I. Kociubczyk, Wilky Desrosin, Lucía Mabel Boycho, Alicia E. Ares, Carlos E. Schvezov

In the present research, commercially pure Sn and Zn, and Sn-Zn alloys (Sn-1wt.%Zn, Sn- 2wt.%Zn, Sn-4wt.%Zn, Sn-8wt.%Zn and Sn-8.9wt.%Zn, weight percent) were obtained by a horizontal directional solidification process with two opposite senses and heat extraction. The solidification process was realized using a horizontal furnace with two heat extraction systems at both ends. The temperature was measured using eight K-type thermocouples and an electronic recorder of temperature data. The resulting structures were analyzed using optical microscopy. From the solidification process the thermal and metallographic parameters were determined in all samples. The presence of defects in the solidified pieces was observed. Internal defects pretended to be dependent not only on the composition of the alloys under consideration but also on the size of the structures formed, also, on the velocities and accelerations of interphases, and on the variation of thermal gradients. A model of the phenomenon from the first principles is presented.

Jan 1, 2015

By Wei Lv, Yang Zhou, Qiang Li, Xuling Chen, Zhiyun Ji, Min Gan, Guojing Wang, Xiaohui Fan

Mineralization during sintering is a process to make part of the raw material melt after serial complex chemical reactions at high temperature. However, high temperature mineralization behavior of the adhesion layer and nucleus particles in the granules during the sintering process has been studied. Research findings reveal that solid-phase reactions between iron ores and fluxes in adhesion layer occurred first, of which the product would induct the generation of the initial liquid phase. By the assimilation of the initial liquid phase, fluxes which served as nucleus particles in granules, such as limestone and dolomite, could dissolve in the liquid phase and extend its amount as increasing temperature, whereas iron ore nuclear particles remained as unfused ores for their insufficient mineralization. Therefore, the mineralization proceeding for sintering was achieved: the iron ores in fine fraction (−0.5 mm) reacted with all fractions of fluxes to form the melt zone, while the coarse iron ores (+0.5 mm) acted as unfused ores, which formed the final sinters together with the melt zone.

Mar 1, 2017

By Yuuki Yoshida

Electrolytic manganese dioxide, EMD, is the positive electrode material of primary batteries and the raw material of LMC used as the positive mass of lithium ion batteries and is currently produced by anodic deposition on and harvesting from a titanium anode in acidic manganese sulfate solutions prepared by dissolving high purity of manganese sulfate into sulfuric acid solutions. This paper presents an alternative method of EMD production using a novel anode, Mn2O3 coated titanium, at lower operating temperature than the current process to explore a possibility of manganese recovery from zinc electrowinning solutions. The Mn2O3/ Ti anode prepared by thermal decomposition of a precursor solution containing Mn (II) showed the anodic deposition of MnO2 by constant current electrolysis and the current efficiency was 95% in maximum, while the current efficiency and the crystallographic structure of deposited MnO2 depended on the current density, the electrolysis time, the bath temperature, and the concentration of Mn(II). The deposited MnO2 was successfully harvested from the anode and the recovery rate was 98%.

By Shaohua Ju

Siderite ore is abundant around the world, due to its inert properties of low grade, mudding when milling and low magnetic, and it is very hard to be beneficiated. Nowadays, decomposition by roasting becomes the main process for utilization of the siderite ore. The methods of energy input for roasting are normally electrical heating, coal or gas combustion. Because traditional roasting methods owns some disadvantiges, such as low energy utilization, high cost and/or large exhaust pollution, only about 10% of the siderite ores in China were used as iron concentrate. In this work, the possibility of roasting siderite ore with microwave energy is studied by both laboratory and pilot experiments. The result of laboratory experiments showed that the optimized condition is roasting for 20 min with a power density of 3 W/g, and the Fe content of the final sample obtained is about 59.12%. The pilot experiments result showed that the decomposition is thoroughly, and the main phases of the roasted material are magnetite and wustite, and the energy consumption of the roasting process is 695.8 KWh/t.

Jan 1, 2014