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By S. J. Macnaughton

The Olympic Dam deposit in South Australia contains 2% copper and 0.06% uranium, which are present as bomite, chalcocite, chalcopyrite, uraninite, coffinite and brannerite. The copper is principally recovered using flotation. The flotation tailings, which contain the bulk of the uranium, and typically 0.3% copper, are leached using sulfuric acid and an oxidant at atmospheric pressure. This paper describes the results from a detailed investigation of the leaching behaviour of this ore. The influence of acid strength, Fe3+ concentration, redox potential and temperature on the dissolution of uranium and copper minerals was studied. Experimental data were obtained from extensive batch leach tests. Mineralogical studies, including SEM analysis of individual mineral grains, were also carried out. The maximum extraction of uranium determined experimentally was in good agreement with that predicted from SEM determination of the proportion of refractory brannerite in the ore. The leaching rate of copper was found to be independent of acidity over the range 20 g L-' to pH 2.0, but was strongly dependent on temperature and Fe3+ concentration. Uranium extraction showed a weak de endence on acidity, Arrhenius temperature dependence and a complex co-dependence on F>+ concentration and redox potential. A kinetic model has been developed, which predicts copper and uranium dissolution. This model will be incorporated into a more comprehensive model that can be used to predict leach performance and reagent consumption for specific ore samples.

Jan 1, 1999

By Robert D. Rogers

The demand for phosphate will continue into the future, because phosphate is currently irreplaceable as a plant nutrient and in many chemical applications. Phosphate is not recycled, so the supply must be replenished through a process of mining and purification. Numerous microbial isolates. obtained from the environment were screened find those which demonstrated the greatest promise of solubilizing PO4 from the ore of interest. Screening was accomplished in a step wise manner an agar plate bioassay, shake flask studies, and semi continuous growth conditions. It was found that with the proper conditions of nutrient supply and solution pH; the bacteria and. fungus used in the semicontinuous process were able to solubilize in excess of 80% of an Idaho rock phosphate ore (RP) within nine days. A significant amount of solubilization occurred within the first six days. There was a 'reasonable correlation between the occurrence of soluble Ca and PO.4 during the processing of the RP thus providing evidence that the RP was being disintegrated by the organisms. In all cases, HPLC analysis of the solutions in which PO4 had been. extracted from RP showed that organic acids, which have been implicated as the mechanism of solubilization, were present.

Jan 1, 1991

By Kuo En Chang

Many rare earth - transition metal (RE-TM) compounds absorb/desorb hydrogen reversibly at room temperature and atmospheric pressure. For LaNi5 which is used as a battery material, the electrochemical nature of this process is well known. In the case of Nd-Fe-B which has found wide application as a powerful permanent magnet, the absorption of hydrogen has both significant advantages and disadvantages. However, a fundamental understanding of the hydrogenation process at ambient temperatures and its effect on subsequent corrosion behavior is currently lacking. This paper reports the results of the hydrogenation of NdFeB two alloys, (NdDy)15Fe78.3A10.7B6 and (NdDy)15Fe67Co5V4A12B7, which are compared with that of LaNi5. Results show that hydrogenation can be accomplished by either electrochemical methods or immersion in dilute sulfuric acid. For the latter method, the change in lattice parameter indicates that the level of hydrogen absorbed by the NdFeB particles corresponds fairly closely to an overall composition of Nd2Fe14BH2.7. Cyclic electrochemical charge/discharge experiments show that the maximum hydrogen discharge capacities of the NdFeB, NdFeB-Co-V, and LaNi5 are 40, 60, and 210 mA?h?g-1, respectively. Anodic potentiodynamic polarization measurements and calculated values of icon reveal that absorbed hydrogen in NdFeB-Co-V and the NdFeB may lead to significant increases in corrosion rates.

Jan 1, 1995

By Chen Song

In the experiments of purifying the solution of chlorine leaching from nickel concentrate with N235, the effects of organic phase composition on purifying efficiency have been studied. From the results obtained, the optimal organic phase composition is found to be 25%N235+12%isomerous alcohol +63%sulfonic kerosene (VIV) and the saturated content of cobalt in organic phase is7.95 g*dm3. And then the serial experiment is carried out. The results show that at the given organic phase composition, the purified solution contains p(Ni) >200 gm dm3, p(Ni)l p(Co) >50000 and the contents of Cu, Fe, Mn, Zn meet the technical criterion of standard nickel electrolyte. The cobalt chloride solution contains p(Co) >I10 g L-1, p(Co) lp(Ni)>50000 and the enrichment of cobalt has been achieved.

Jan 1, 2006

By May Nyman

Due to the vast diversity of chemical media in which metal separations are executed, a wide range of ion separation materials are employed, This ,results in an ongoing effort to discover new phases with novel ion exchange properties. We present here the synthesis of a novel class at, thermally and chemically stable microporous, niobate-based materials. Ion exchange studies show these new phases are highly selective for Sr2+ and other bivalent metals.

Jan 1, 1999

By J. T. I. Poijärvi

Outokumpu Harjavalta Metals Oy operates copper and nickel smelters, three sulphuric acid plants and nickel refinery at Harjavalta and copper refinery and precious metal plant at Pori. The by-products of these plants are presented in this paper. The by-products of the smelters include products from slag cleaning of flash smelting furnaces and converters, flue dusts and smelter off-gases. Weak acid and sludges from cleaning of smelter off-gases and acids are the by-products of the acid plants. The by-products out of the copper refinery are crystallized metal sulphates and sludges from electrolyte purification, on which a co-production process of the copper tankhouse is based. The main by-products of the precious metals plant are products from anode slime treatment and platinum metal group concentrates in the recovery of precious metals. Sludges from nickel matte leaching and precipitates from solution purification are the by-products of the nickel refinery. The formation, treatment and processing as well as the research work done for the utilization instead of dumping of the by-products in the production of copper and nickel will also be discussed in this paper.

Jan 1, 1995

By Jinxia Nie, Yunnen Chen, Dachao Zhang

"Rare earth resources are strategic and non-renewable resources. But disordered exploitation on rare earth metals leads to resources waste, environmental pollution and ecosystem destroyed. In this paper, soil collected from garden was cultured in thermostated incubator. Adding exogenous rare earth to the soil and the effects of recombination action of rare earth lanthanum, cerium and yttrium on soil enzymatic activities were studied. The results showed that single metal La and Ce can increase urease activity, but Y inhibits its. Coexist La/Y or La/Ce in soil inhibit the urease activity, coexist Y /Ce or coexist three metals promote its. Single metal La, Y and Ce can promote catalase activity, and that of coexist three metals. Pairwise coexist La, Y, Ce in soil inhibit catalase activity. With certain concentration of rare earth recombination action, urease activity in soil has been very significant direct proportion to ionic impulse, but catalase activity been insignificant inverse proportion to its.1. IntroductionThe increase of rare earth element content due to anthropogenic inputs frequently takes place in agro-industrial areas, leading to soil pollution episodes that may cause serious environmental problems because of their potential toxicity to microorganisms, plants, animals and human beings [ 1]. China is abundant in lanthanides resources. Rare earth metals are used in many frontier technologies such as photic devices, magnetic materials, and fine ceramics, and the amount of the rare earth metals used in these industries has been increasing. In addition to their use in industry, rare earth metals are more widely applied to cropland as microelement fertilizers due to their ability to promote growth and productivity of some crops [2]. As a result, more and more rare earth metals are moving into the ecosystems. While a permanent contamination of soils results in populations of micro-organisms with high resistance to rare earth metals, a short-term burden of contaminants at high concentrations could exert inhibitory effects on microbial carbon [3]. They accumulate in soils, bioaccumulate in crops, and enter the food chain, causing a potential problem of rare earth metals environmental pollution in China [4]. This contamination may also severely influence organisms and soil activities [5]."

Jan 1, 2011

By Vladimir I. Skorohodov

The technology for copper utilization from circuit boards etching is proposed. The technology is based on combination of electrochemical and sorption methods. The conditions of copper electroextraction from ammonia-chloride solutions with obtaining of cathode copper are defined. The stage of electrolysis is destined for copper recuperation from etching process. Due to the electrochemical processes are unacceptable for cathode precipitation of the copper from diluted solutions such as rinse waters, the concentration on the strong-based cationites are used. After filtration throw the sorption columns solution is directed to the stage of circuit boards washing. It allows organizing close loop water recirculation. After saturation. resin is 'regenerated by chloride ammonium solutions. Obtained eluate directed to the etching stage, Generally. the technology provides copper recuperation and minimize wastes amount.

Jan 1, 2001

By Huayi Yin, Wang. Dihua, Wei Xiao, Xuhui Mao, Diyong Tang

"The world production of crude steel reached 1.55 billion tons in 2012,which generated ~2.5 billion tons of CO2. Electrochemical metallurgy especially through high temperature molten salt electrolysis with renewable electricity stands for a great opportunity for producing “green” metals. In recent years, electrolytic production of iron without emission of CO2 in different molten salt systems has been reported. A cost-affordable inert anode is the key to produce acceptable eco-friendly iron by the novel molten salt electrolysis processes. Based on the authors’ research, this paper will discuss iron production by molten salt electrolysis using a nickel alloy inert anode. On the other hand, the paper also covers a novel molten salt CO2 capture and electrochemical transformation (MSCC-ET) process, in which CO2 is effectively converted to value-added carbon and oxygen in a molten bath using a cost-affordable nonconsumable SnO2 anode.1. IntroductionEnergy and materials are cornerstones to support the development of human society. The traditional primary metal production, especially iron and steel, and electricity production are mainly based on the reactions between carbon (coal) and oxygen (represented by equations (1) and (2) respectively), which produce huge amount of CO2.MxOy + 0.5y C = x M + 0.5y CO2 (g) + Q1 ( 1 )C + O2 (g) = CO2 (g) + Q2 ( 2 )In 2012, the world production of crude steel reached 1.55 billion tons, of which 46.3 %, ~0.7165 billion tons were produced in China. Based on the average level of 1.7t CO2 emission per ton steel, more than 1 billion tons of CO2 generated from steel industry in China in the year. Besides the iron and steel industry, thermal power plant leads the CO2 emission in both USA and China. The total consumed electricity in China increased to 4959 billion kWh in 2012, ~70% of it was from coal fired power plant. The average CO2 emission for electricity production in the typical thermal power plant in China is around 0.78 kg kWh-1. It accounts for ~ 3.868 billion tons of CO2 emission from thermal power plant in 2012 in China."

Jan 1, 2014

By Zhenyang Wang, Xingle Liu, Xiangdong Xing, Shan Ren, Hongen Xie, Jianliang Zhang

"Non-isothermal combustion experiments of different additive amount of bituminous (0, 20, 40, 60, 80, 100 wt%) were conducted by synthesized thermogravimetry analyzer(STA409PC) from room temperature to 900°C in air. The changes of combustion characteristic parameters o f pulverized coals in different atmospheres are analyzed. The results show that DTG curves of coal combustion move to low temperature zones when the amount of bituminous increases. It indicates that both ignition and burnout temperature are lower, burnout time decreases, combustion characteristic index obviously increases, and combustion performance of blending coal are improved. The iso-conversional method involving Kissinger-Akah-Sunose (KAS) method was used for the kinetic analysis of the main combustion process. The results indicated that, when the additive amount of bituminous varied from 0 to 100 wt%, the value of activation energy which would sharply reduce if the additive amount of bituminous was under 60% increased from 133.94 kJ•mol-1 to 78.03 kJ•mol-1by using KAS method.IntroductionPulverized coal injection (PCI) to blast furnace (BF) is an important way for saving energy and reducing resource consumption during the ironmaking process. In order to acquire higher coal injection quantity, the relevant research topics in the field of pulverized coal combustion technology such as enhancing the efficiency of pulverized coal combustion, improving the combustion characteristics and reducing the harmful gas emissions and so on received extensive attention in recent years [1,2]. The combustion of blending coal when the appropriate proportion is selected for coal and also mixed well- distributed could give full play to the advantages of various types to make up the defects of single coal which is widely used throughout the world. So the blending coal injection to BF could produce a good impact on safety and economy for productive process. Therefore, a large amount of experimental researches on the combustion characteristic of blending coal for anthracite and bituminous were carried out by experts and scholars around the world [2-7].Nevertheless, the systematic research on the combustion behavior of anthracite with different content of bitumite in a thermogravimetric analyzer (TGA) is less. So in this paper, using the method of multiple scanning rate of conversion method, bituminous to promote the pulverized coal combustion reaction was studied to analyze its promotion mechanism of pulverized coal combustion reaction process, and the kinetic parameters of activation energy was also calculated, which to provide theoretical basis for the rationalization of resource utilization."

Jan 1, 2014

By Minjun Tang, Jianfeng Zhou, Feng Chen, Linjiang Qing, Xiaolei Song, Yufeng Guo, Tao Jiang

"Reduction swellability index (Rsn and low temperature reduction disintegration index (RDI) of vanadium-titanium magnetite oxidized pellets are harmful to the processing of ironmaking, for example, causing serious gas permeability, decreased yield, higher coke ratio and more furnace dust. Thus, the improvements of RSI and RDI of vanadium-titanium magnetite oxidized pellets were investigated in this paper, including the pretreatment of raw material, additives of dolomite or boric acid, pellets treated in chloride solution and so on. The results showed that damp milling as pretreatment and boric acid added in pelletizing were conducive to the RSI which decreased 5% and 7% respectively, while they were not efficient enough in improving RDI. Dolomite was efficient in improving RSI, but had negative effect on RDI. There was no evidence to show that RSI and RDI would be improved when pellets were treated in chloride solution. Pursuing this further, the mechanism of those improvements were investigated.IntroductionIn the world, vanadium-titanium magnetite utilization is investigated around how to recover iron, titanium, vanadium, and divided into blast-furnace method and non-blast-furnace method according to respective characteristics. Blast furnace method [1, 2] can recover iron and vanadium effectively, but Ti02 cannot be recycled. Non-blast-furnace methods include rotary kiln-electric furnace method, pre-reduction electric furnace method, reduction- grinding method and sodium vanadium-rotary kiln-electric furnace method and so on. [3-7]Comparing to the Non-blast-furnace method, the method of blast furnace smelting has been put into industrial applications. And it has the following advantages: First of all, effective recycling iron and vanadium; Second, technical problems of high titanium slag in blast furnace smelting; Third, it has mature technology in blast furnace smelting."

Jan 1, 2013

By M. Misra

The removal of lead and other heavy metals present in an active US Army small arms firing range soil was evaluated in a pilot scale test program at Ft. Polk, Louisiana. Two different acid based extraction processes in conjunction with conventional physical separation methods were used. Physical separation processes consisting of screening and gravity operations removed most of the coarse lead particulates and slugs. Hydrochloric acid leaching followed by precipitation of lead as hydroxide recycled clean soil containing less than 500 mg/L. total lead and less than 5 mg/L TCLP lead. Lead extraction efficiency with hydrochloric acid was 96 percent. The results of lead removal by physical separation in conjunction with acetic acid leaching were not consistent over the whole test period and the total soil processed.

Jan 1, 1998

By D. Y. Wang, G. Y. Sha, X. L. Shen, D. R. Gu

The study of the volatilization kinetics of zinc and lead in pellets made of zinc-leadbearing dust mixed with coal powder, in a nitrogen atmosphere and at a temperature range between 1100 °C and 1300 °C, shows that the reduction temperature has a significant effect on the volatilization rates of zinc and lead, and that both the particle size of the coal powder and the extra carbon content has no effect on the volatilization rates. The obtained activation energies for the volatilization of zinc and lead are 79.42kJ/mol and 88.74kJ/mol respectively. The volatilization rate of zinc is controlled by the reaction between the zinc oxide and carbon monoxide while that of lead is controlled by the lead evaporation reaction, and the diffusion of gaseous lead through the gas boundary layer covering the surface of the reduced liquid lead.

Jan 1, 2000

By J. B. Winter

The present Inspiration Consolidated Copper Company Smelter/Acid Plant complex located near Miami, Arizona, was designed and built specifically to conform to the ambient air quality standards imposed by the Federal Clean Air Act of 1971. The present plant replaced a facility which had been in operation since 1915. The electric furnace, siphon converters and acid plant complex were commissioned in May, 1974 (1). At that time, the Plant was considered to be one of the most extensively monitored and instrumented facilities of its kind in the world. Several control areas were located in close proximity to the controlled process, in addition to so-called central control rooms in the Smelter and Acid Plant. The control rooms were staffed with officials below the foreman level. Instrumentation consisted of conventional analog devices, except for a computer used in monitoring ambient air environmental conditions and limited use of programmable logic controllers. The harsh service conditions prevalent in the plant rendered a significant portion of the instrumentation unreliable and, in many cases, inoperable. Failure of the facility to obtain the total sulfur collection for which it was designed was, in part, due to serious inadequacies in control system logic and sulfur recovery averaged 79% in the early years. After careful study of the smelting process, engineering hardware and high labor cost inherent in the organizational structure, management made a judgement decision to convert to centralized control of the process with high level supervision 24 hours per day. A distributed digital control system with supervisory arid data acquisition/information reporting computers was selected to satisfy the requirement of central control. Operations are now controlled and coordinated from a primary control room in the Smelter and a satellite control area in the Acid Plant.

Jan 1, 1983

By A. R. Udupa

The reduction roasting behavior of chalcopyrite has been investigated using various combinations of a desulfurizing agent, i.e., CaO or Na2CO3, and a reductant, i.e., CO, H2 or C. Using these, combinations the sulfur is removed from the mineral as CaS or Na2S rather than SO2 as is the case with conventional copper smelting and converting. The laboratory reduction ex¬periments were conducted using thermogravimetric analysis (TGA) and boat tests of mixed combinations of fine particulate reactants subjected to a continuous gas stream. The degrees of metallization were determined by both weight loss and chemical analysis methods and the products examined using optical and scanning electron microscopy and electron probe microanalysis. The percent reduction after one hour at 900°C ranged from 60% to 94%. From these data It was possible to provide postulations as to the controlling reduction mechanisms.

Jan 1, 1983

Thallium is a very minor element found in lead ores. It's behaviour during lead smelting has recently become of much greater interest due to the effects it had on the health of waste heat boiler maintenance contractors at a Canadian smelter. In this paper the behaviour of thallium in both traditional and direct lead smelting processes will be examined using computational thermodynamics techniques. Yazawa and his coworkers have made extensive use of computational thermodynamics to examine and illustrate pyrometallurgical processes. It has been shown that thallium behaviour during smelting is strongly influenced by the extent of oxidation of the lead concentrate and by the presence or absence of chlorine in the charge. The condensation behaviour of thallium species in the waste gas handling system was also modelled and it has been confirmed thallium-rich deposits can form at the high temperatures prevailing in waste heat boilers.

Jan 1, 2003

By Shu-cai Zhou

"To understand the solidification behavior of austenitic heat-resistant stainless steel (TP34 7) in rotary electromagnetic-field, the influence of electromagnetic stirring in mold (M-EMS) on solidification structure of TP34 7 heat resistant steel in a round billet continuous casting was investigated based on industrial experiments. The results indicate that the excellent billet solidification structure of TP34 7 heat resistant steel can be obtained with appropriate electromagnetic stirring parameters. The solidification structure of TP34 7 heat resistant steel can be remarkably refmed, central porosity and shrinkage cavity can be remarkably decreased and equiaxed grains zone widens was enlarged. The industrial trials verify that the stirring intensity of TP34 7 heat resistant austenitic stainless steel should be higher comparing with plain carbon steel. Due to a higher viscosity, rotating speed of molten stainless steel was 20-30% lower than that of molten carbon steel in the same magnetic flux density.IntroductionIn recent years, the development of ultra super critical (USC) plants is accelerated by the demands of environment protection and energy saving, and USC plants with steam temperature and pressure conditions in excess of 593°C and 24.lMPa respectively were constructed. To achieve the goal, it is important to develop new materials with excellent high temperature strength, superior resistance to oxidation and corrosion at high temperature. Besides, their cost must be low enough to meet the requirement of plants [ 1]. TP34 7H steel is promising austenitic heat-resistant steel, which is used as superheater/reheater tube material and is extensively used for high temperature components and fossil-fired power plants, and suitable to be used in USC boilers plant. This kind steel contains with about 0. 7%Nb and it keeps higher allowable stress and creep rupture strength than TP304 and TP321H [1-2]. TP347H has conventionally been produced by ingot casting followed by forging and rolling. Recently, in order to decrease the production cost, challenging trials to produce these types of alloys by a continuous casting (CC) process have been attempted. However, the solidification structure of austenitic stainless steel is one of the key issues that attract more attention. Due to the low thermal conductivity of TP347H heat resistant stainless steel (much smaller than that of plain carbon steel), pronounced defects during continuous casting of austenitic heat-resistant steel such as coarse columnar, center porosity and coarse bridging, greatly influence mechanical properties of fmished products.A widely used technique in metallurgy is the inductive drive of molten metals using rotational or traveling magnetic fields. Recently, rotary electromagnetic stirring (EMS) has been applied to reducing various defects and improving increase the solidification structure of the metals in the continuous casting of steel, Al-based alloys and Mg-based alloys [3-8]. Electromagnetic stirring of plain carbon and low alloy steel in the continuous casting bloom and slab is well established for improving the quality of cast products [9-11] and is widely used in industry. However, very few literatures on electromagnetic casting of heat resistant stainless steel have reported. In this work, an industrial plant trial was performed to clarify the effect ofM-EMS on the macroscopic quality ofTP347heat resistant steel billet, in which the regularity and mechanism of the influence of EMS on solidification casting billet were discussed."

Jan 1, 2014

By Toshiaki Akahoshi

Keywords: Wasted catalyst, Hydrodesulfurization, Ammonium vanadate, Ammonium molyb-date, Hydrometallurgical process. The fundamental reactions have been investigated in order to develop a hydrometallurgical process for recovery of molybdenum and vanadium from wasted catalysts generated in the hy-drotreating desulfurization of heavy oil. The principal steps of the process are a mild oxidation roasting of the waste catalysts at temperature around 500°C, leaching of the target metal components with dilute ammoniacal aqueous leachates, selective precipitation of vanadic acid, and ammonium molybdate precipitation. The selective recovery of vanadium as vanadic acid is successfully performed using ammonium sulfate as a salting-out agent. Recovery of ammonium molybdate is based on large dependence of solubility of ammonium molybdate in ammoniacal solutions upon temperature and ammonium salt concentration. In this process, the solution after recovery of vanadium and molybdenum is recycled to the leaching stage of the roasted materials, and the ammonium salts in the process liquor is in the repeated use. Employment of am-moniacal system makes it possible to operate the roasting at much lower temperature than that for the currently operating process.

Jan 1, 2005

By Nicole de Jager, Michael J. Nicol

"In order to liberate gold from refractory gold ores and concentrates it is generally necessary to oxidise the surrounding sulphide minerals, typically pyrite and arsenopyrite. Traditional methods of oxidation include pressure leaching, roasting and bacterial oxidation. In recent years, bacterial and pressure oxidation have found increasing favour, although these methods are by no means completely satisfactory and each is subject to particular disadvantages.A novel process has been developed as an alternative to the traditional methods whereby electro-generated ferrate(VI) ions in alkaline solution are used to oxidise a pyrite concentrate. This process has been observed to proceed fairly rapidly and could prove to be a more economically viable process, as well as being more environmentally acceptable. As an added benefit, operating in an alkaline environment is advantageous for downstream cyanidation processes.Ferrate(VI) is a relatively unknown species, due mainly to its instability in acidic solutions. However, in alkaline solution it has been observed to be sufficiently stable for use as an oxidant when used under favourable conditions. Ferrate(VI) is most conveniently manufactured electrolytically via the dissolution of high-carbon anodes in strongly alkaline solutions. Some literature has been published on the electrolytic generation of ferrate(VI) and relatively high efficiencies have been observed by both the authors and other researchers.This study utilises both electrochemical techniques and leaching experiments to examine the kinetics of the oxidation of pyrite by ferrate(VI), which is produced electrolytically. Cyclic voltammetry, rotating disk voltammetry and potential step experiments have been used to investigate the kinetics and mechanism of the oxidation process."

Jan 1, 1997

By René Winand

Due to chemical and electrochemical behavior of the most common additives in copper electrorefining i.e. gelatine, thiourea and chloride ions, it is essential to simulate as far as possible true industrial practice while performing laboratory experiments. The three additives must be studied simultaneously, and added continuously to the electrorefining cell. Ratio electrolyte volume to cathode area; ratio bleed flow to cathode area; hydrodynamic conditions; residence time of electrolyte in the cell; current density; electrolyte and soluble anode must be as near as possible to industrial ones. Experiments performed in the author's laboratory show that under these conditions, reproducible results can be obtained at normal industrial current density and at high current density as well. Problems are however still encountered when developing a sensor for additives monitoring, due to electrolyte redox potential and to substrate influenced thin layer deposition.

Jan 1, 1995