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By W. F. Drinkard

Many in the environmental movement have focused on this element. But, nothing they or anyone does will change the amount of arsenic in the world. This report is on actual commercial plants that we developed and operated to recover or stabilize arsenic values from metallurgical dusts from gold and copper pyro operations and arsenical gold bearing ores. When they were available gold and copper values were recovered. Our experience in arsenic extends over thirty years. My first corporation, Mineral Research & Development Corporation was the first in North America to manufacture the then new CCA (copper-chrome-arsenic) wood preservatives. This class of wood preservatives proved to be so effective that it made wood into an entirely new material of construction. It is not uncommon for wood properly treated with arsenical CCA preservatives to last for thirty; forty, and sixty years. Over a hundred years have been projected in some field tests. Hundreds of thousands of trees have been saved. Millions more trees would have been saved had environmentalists not decided that their arsenic phobia was more important than trees. There are several variations of CCA. The most popular is CCA-C. Its formula is: CrO3 . . . . . . . . . . . . . . . . . . . 47.5% CuO . . . . . . . . . . . . . . . . . . . 18.5% As2O5 . . . . . . . . . . . . . . . . . 34.0% Until recent restrictions were placed on the consumption of arsenical wood preservatives, annual consumption in North America was about 150,000,000 lbs./yr. About 64,500,000 of arsenic as the pentoxide was safely consumed this way. World CCA consumption has been about double the above figures or 300,000,000 lbs. as 100% CCA and 129,000,000 lbs/yr as As2O5. Close to 100% of all the arsenic used in wood preservatives is derived from gold or copper processing. The valence of arsenic required for CCA wood preservatives and many other markets is the same valence that is required for stabilization. The economic challenge is how to get there. We have built and operated eleven plants to oxidize arsenic trioxide to its pentavalent form. Most of these have been classic in that they used a common oxidants such as hydrogen peroxide or nitric acid to achieve this.

Jan 1, 2005

The paper describes the propensity of tin to form intermetallic compounds with microalloying elements such as Nb, Ti and aluminium, which are commonly used as additions to achieve particular combination of strength and toughness. Two series of alloys were prepared by arc melting under an argon atmosphere. Each series was based on Fe, Sn and A1 with either Nb or Ti additions. The microstructures were studied using scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy and microprobe analysis. It was found that the level of Nb addition has an effect on the formation of Sn-rich compounds. For small Nb additions, no Sn containing compounds were found, whereas in higher Nb alloy, a Laves phase (FezNb, hexagonal, a = 0.4830 nm and c = 0.7879 nm) containing about 1 at % Sn was found. A FezNb3 phase (cubic, a = 1.1261 nm) associated with the formation of alumina was also found but did not contain tin. No Sn containing compounds were found with Ti additions. The experimental observations have been compared with thermodynamic calculations performed using MTDATA.

Jan 1, 1999

By Zhigan Deng

Cooling crystallization was used to separate iron (III) and nickel (II) from acidic sulfate solution produced by leaching of molybdenum-nickel black shale. The effect of K2SO4 concentration, crystallization temperature, solution pH and crystallization time on recovery of nickel (II) and precipitation of iron (III) was investigated, in order to obtain effective separation of nickel and iron. The optimum parameters determined were as follows: 200 g/L K2SO4, 10 °C crystallization temperature, solution pH of 0.5 and 24 h crystallization. Under these conditions, 97.6% nickel (II) was recovered as K2Ni(SO4)2, 6H2O crystals and only 2.0% of the total iron (III) was precipitated. Recrystallization yielded K2Ni(SO4)2, 6H2O crystals with a purity of 98.4%.

By Liuyin Shi, Kang Liu, Fengqi Zhao, Yan Song, Zhiping Yang, Xing Fan

Due to the high energy consumption, long technical process, low usage rate of vanadium during the traditional smelting vanadium steel process, a new method for decarburization by CO2 to directly smelt vanadium-containing steel in blast furnace was proposed. In this paper, the thermodynamics of CO2 decarburization in molten iron process was calculated out by FactSage. The thermodynamic calculations indicated that in standard state, the transformation temperature of C and V was 1357 °C; the oxidation order of element was Si, C, V, Mn and S when using CO2 as oxidant. The experiment of blowing CO2 temperature showed that decarburization reaction temperature was 1550 °C, carbon content could be decreased to 0.676%, the decarburization rate was 88%. There was no effect on vanadium content in molten iron during the decarburization process, vanadium content was 0.323%, which meets the request of vanadium mould steel.

Mar 1, 2018

By Xia Zhao, Yong Zhao, Wen Pan, Ze-jun Ma, Yan-juan Yang

Characteristics of the gas-solid reduction reaction between iron ore sinter and carbon monoxide (CO) gas at 1273 K were studied with thermogravimetric analyzer. The microstructure, mineral compositions and porosity of sample were investigated prior to reduction, in the 30% reduced sample, in the 70% reduced sample, and in the fully reduced sample. At the reduction degree of 30%, the hematite and calcium ferrite was reduced to 44.4 and 60.4% respectively. At the reduction degree of 70%, all the hematite, calcium ferrite and magnetite were reduced to metal iron, only 36% wustite was left in the core area. The reduction reaction began with the loose structures and spread to the nearby area. In the area of micropores, the reducing gas can easily diffuse to the reaction interface to proceed the reduction reaction effectively. So increasing the content of micro-pores is an effective way to improve the reducibility of the sinter.

Mar 1, 2018

By Huimin Lu, Min Li, Jinghua Zou

"Zeolitic imidazolate frameworks (ZIFs) are new type of porous materials, form inerratic polyhedral in three-dimensional with large cages and small apertures, and appear structural diversity. Their hole size can be adjusted. These materials have high selective adsorption capacity to carbon dioxide. In this paper, zeolitic imidazolate frameworks were synthesized by solvothermal synthesis method with dimethylformamide (DMF) as solvent and structuredirecting agent, divalent metallic ions as cation, and imidazole as ligand. The crystals were characterized with XRD, SEM for their crystal structures and physical properties, the adsorption of the crystals for carbon dioxide was also tested, and the result suggests that these porous materials have a capacity of 1.35ml/g for storing carbon dioxide at 273 Kelvin under ambient pressure.IntroductionGlobal warming caused by the increase of carbon dioxide in the atmosphere has become one of the main environment problems, contemporary research has focused on ways to slow or stop this trend. CO2 capture has attracted attention due to the potential to trap and sequester large amounts of CO2 from concentrated sources such as power plants [1]. Traditional technologies in capturing CO2 include absorption by aqueous amines [2]. However, utilization of this process is energy intensive and expensive. Carbon dioxide storage materials investigated so far can be divided into two categories: chemical storage adsorbents and physical storage media [3]. The first kind of materials can chemically adsorb carbon dioxide within their structures and need thermal energy to release the adsorbed carbon dioxide. The examples of the chemical adsorbents include aqueous amines, gas-hyperbranched aminosilicas [4]. The physical adsorbents store carbon dioxide by physical adsorption of carbon dioxide at elevated pressure and release the adsorbed carbon dioxide at low pressure. The physical adsorbents that have been investigated for carbon dioxide storage include zeolites, carbonaceous materials and other porous materials. Until recently, a new type of microporous material, known as zeolitic imidazolate frameworks (ZIFs), has been reported as promising adsorbents for carbon dioxide storage [5 ~ 10]."

Jan 1, 2010

By Upali Siriwardane, Tushar V. Kudale, Naidu V. Seetala

"Cellulose acetate (CA) membranes with 25% triethyl citrate (TEC) as plasticizer were prepared with varying thickness for CO2 gas separation from water-gas-shift (WGS) reaction products. The AFM analysis of the CA membrane showed that the uniform coating had fewer and smaller pores as the film thickness increased, and corroborated by gas permeability studies. The CO2 permeability has decreased faster than CO permeability with the CA/TEC membrane thickness, and findings support that the CA membrane could be used to entrap CO2. Several CA/TEC membranes were also staked to increase the separation efficiency. Positron Annihilation Lifetime Spectroscopy (PALS) was used to estimate the nano-porosity (pore size and concentration) changes of CA/TEC films. PALS results show a decrease in pore size with increasing CA-TEC concentration in acetone, while the pore concentration increases. The PALS results are correlated with the CO2/CO permeability variations as the CA-TEC concentration change.IntroductionHydrogen is one of the main energy sources available for the future advancement of clean fuel technologies especially for fuel cells. Generation of hydrogen and CO2 from Water Gas Shift (WGS) reaction mixtures of CO and H2O is of interest to many researchers since it allows a large scale production of hydrogen [1, 2]. Once hydrogen is produced using the WGS reaction, the output products contain mixture of CO, CO2, H2, and water vapor. Metallic membranes have been used as hydrogen separation membranes [3-6]. As H2 is separated from the mixture using the metal membranes, we need to separate CO2, and find ways of sequestration of CO2 to avoid environmental problems by greenhouse gasses. Polymeric Membranes have been used for CO2 separation [7]. Plasticizer can control the micro-structural properties such as pore size and concentration of polymer membranes [8], which influence the size/molecular weight dependent diffusion rates of the gas molecules. We have used cellulose acetate with triethyl citrate as plasticizer to separate CO2 from the WGS reaction products. Positron annihilation lifetime spectroscopy (PALS) is very sensitive and able to identify different kinds of defects and their agglomerates such as vacancies, vacancy loops, and voids [9, 10]. PALS has been successful in determining the free volume in polymers that influence the properties of the polymers [11, 12]. Microscopic properties of the free volume obtained from PALS have been correlated to macroscopic properties [13, 14]. We used PALS to study the nanoporosity (pore size and concentration) and fractional free volume changes of CA/TEC films, and used to understand the variations observed in the CO2/CO permeability as the CA-TEC concentration in the membranes change."

Jan 1, 2014

By K. Morsi, S. K. Kassegne, K. S. Moon, A. Numula

"Current Activated Tip-based Sintering (CATS) is a new process for the powder-based manufacturing of macro, micro and possibly nano-scale features and shapes. CATS enables the selective sintering of powders by localizing current activation conditions through an electrically conducting small tip (either in the stationary or moving mode). This paper presents preliminary experimental results on the CATS of reactive mixtures of Ni/Al powder to form nickel aluminide intermetallics. Preliminary investigations on the effect of current on the reaction characteristics are discussed.IntroductionSpark Plasma Sintering (SPS) has been the subject of intense research over the past decade [1,2, 3,4,5,6]. The process boasts remarkable advantages which include ultra fast heating rates (hence by-passing low temperature non-densifying sintering mechanisms), considerably lower sintering temperatures and shorter sintering times than achieved in conventional sintering. The process is however limited to the generation of simple geometries on the macro-scale. Recently three of the authors conducted work on a novel process ""Current-activated tip-based sintering (CATS)"" [7], where electric current is passed through a conducting tip that is placed or allowed to travel over a powder bed/compact to locally sinter powders. lD, 2D and 3D micro-scale sintered shapes can be generated with the possibility of 3D rapid prototyping on the macro/micro or nano-scale. Although CA TS of single phase powders has been conducted, the CATS of reactive powders has not yet been investigated.The Ni-Al phase diagram contains five intermetallic compounds, AhNi, AhNh, AlNi, AhNi5 and NhAl. Out of these intermetallics, NiAl and NhAl have received the vast majority of scientific and industrial interest [8]. NhAl can be formed by reaction synthesis, where nickel and aluminum reactant powders are heated to a reaction ignition temperature at which the reactant powders are converted to the intended intermetallic product. The reaction is exothermic which gives rise to considerable compact self heating, thus instantaneously raising the compact temperature by several hundred degrees which facilitates sintering [8]. Applying and electric current locally would not only provide for a rapid local reactive sintering, but would generate a number of intriguing scientific investigations. For example, of interest would be, how would the reaction propagation and microstructural/phase evolution be affected by the temporal and spatial temperature and current distributions."

Jan 1, 2011

By Alexander Burns

Electrolytic salt splitting is a technology where acid and/or base is regenerated from a neutral salt using membrane electrolysis. Recent advances in the understanding of brine treatment, membrane stability, and cell design have made electrolytic salt splitting feasible on certain hydrometallurgical solutions. Meanwhile, environmental regulations have made the bulk disposal of salt solutions more difficult. In this paper, sodium sulfate salt splitting is examined from a cost perspective, compared to purchasing the reagents directly. Relative costs are estimated for several regions based on published electricity and reagent prices. The results show that salt splitting is economically favourable in some regions, and can be made more favourable by applying modifications to the traditional three-compartment desig

By Andrzej Warczok

Intensive smelting of copper concentrate in Teniente Converter (CT) leads to the production of high grade matte and highly oxidized slag. Smelting slag is processed in Teniente vascular slag cleaning furnace. The slag composition and forms of copper affect the slag cleaning process and final copper content. Converting of high grade matte in Pierce-Smith converter faces some difficulties in proper slagging of iron oxides. Overblowing in copper making stage allows for slag liquidation but leads to high content of copper oxide in converter slag. Converter slag recycling into CT results in the increase of the participation of oxidic copper. Separate treatment of converter slag and its impact on the forms of copper in CT slag has been analyzed. Thermodynamic properties of a system and kinetic limitations pointed out the negative effect of converter slag recycling on the forms of copper and copper recovery in slag cleaning stage. Experimental results of slag cleaning tests in a crucible scale as well as microscopic examination of laboratory and industrial slag samples supported the above analysis and permitted to formulate recommendations of separate processing of converter slag. Keywords: copper, losses, slag, recycling

Jan 1, 2001

By Kenneth L. Reid

The Mineral Resources Research Center at the University of Minnesota has recently installed a QEM*SEM system (Quantitative E.valuation of Materials using Scanning Electron Microscopy) to aid in detailed mineralogical evaluation of potential mineral resource developments in Minnesota and to provide services to the North American mineral industry. A primary application for the unit is to serve the Minnesota taconite industry by providing mineralogical analysis of ores and concentrator products. Minnesota taconite ores contain fine-grained magnetite in a quartz matrix. The ores undergo several size-reduction/magnetic-separation steps to produce a final concentrate with approximately 75% passing 325 mesh and containing about 5% gangue. The paper describes a typical taconite concentrator flowsheet and reports some preliminary results of the applications of QEM*SEM particle image maps and cumulative yield liberation data to samples from selected points in the concentrator circuit.

Jan 1, 1988

By Dominik Hofer

A broad spectrum of tantalum containing input materials can be processed for the production of synthetic tantalum concentrate (“SynCon”). The use of these low grade substances offers a secure alternative to mining of coltan in Central Africa. SynCon is produced in a multi-stage pyrometallurgical process, wherefore the melting behaviour of slags presents an important factor especially regarding the energy consumption and its optimisation. The characteristics of a slag comprising mostly Al2O3, CaO, SiO2 and MgO are influenced by the amount of other oxidic constituents which enfolds the main focus of this study. A hot stage microscope serves for the investigation of the slag behaviour in a temperature range from 1000 to 1600 °C under reducing atmosphere (CO/CO2 gas). The experimental results are compared with thermodynamic calculations (FactSage) to get a better understanding of the process.

By Kazuki Morita

A new route to produce solar grade silicon (SOG-Si 6N) from metallurgical grade (MG-Si 98%) has been developed in Japan, which may satisfy the increasing demand for solar cells in the near future. Since some elements such as P and B have very large segregation coefficients, solidification refining is not effective for their removal and costly processes, such as electron beam vacuum melting and oxidation plasma refining, are required. According to our previous results which showed the effectiveness of leaching procedure with Ca addition for Fe and Ti removal, possibility of P and B removal by acid leaching was focused expecting that their affinities for Ca in molten silicon might be considerable. Hence, the effects of Ca addition on the thennodynamic properties of P and B in molten silicon alloys have been investigated for overall control and optimization of the SOG-Si production process in the present study. The interaction parameters between Ca and P, and Ca and B were determined by chemical equilibration techniques at 1723 K. Although the interaction parameter between Ca and B was slightly negative, that between Ca and P showed a large negative value. Also, the results for the leaching test with various amount of Ca addition revealed that the removal fractions of both elements, especially P, drastically increased with increase in the Ca content, which showed very good agreement with the prediction from the interaction parameters derived in the present work. The present results suggest that the preliminary leaching procedure can reduce the processing time and energy for SOG-Si refining. Keywords: Silicon, Solar Cell, Refining, Acid Leaching, Thennodynamics. Interaction, Phosphorus, Boron, Calcium

Jan 1, 2003

By Jose R. Parga

In mining operations, cyanidation is the ,predominant method by which gold and silver are recovered from their ores and it is recognized that cyanide consumption can be a major factor that contributes to the operating costs for such operations. Also after extraction and recovery of precious metals a certain amount of cyanide is delivered to the tailings pond and must be considered with respect is environmental problems due to the toxicity of cyanides. In this regard, the Air-Sparged Hydrocyclone (ASH) has been used as a reactor for the treatment of cyanide solutions in two ways; first for cyanide recovery by acidulation using the Mexican modification of the Mills-Crowe process and second for cyanide destruction by oxidation with the use of chlorine dioxide (ClO2). In both cases, excellent performance can be achieved using the high capacity ASH system.

Jan 1, 1998

By Mokka N. Rao

In this experimental investigation, the principal operating parameters of the spirals HC 1870 and HG 8/7 are determined for the hydrogravimetric separation of the friable siliceous iron minerals of the Piar Distric, Venezuela. Mineralogical characterization including optical microscopy of feeding materials and the products after separation are presented. Comparative analysis is made of effectiveness of productivity between the two spirals.

Jan 1, 1999

By Kenji Monden

A simple technique is presented to evaluate optical property of biomimetic microlens array (BMA) as an antireflective surface on a polydimethylsiloxane (PDMS) sheet. The integration of these structures is done by a thermoforming process. We have only UV-VIS spectrophotometer for optical evaluation apparatus. The transmittance of the sheet is measured with angled sample holder. The 50 deg. transmittance of 270nm pitch BMA on PDMS sheet increases from 87 to 92% after the moth-eye structure is introduced. The transmittance of 350nm pitch BMA on PDMS sheet increases from 87 to 96% after the moth-eye structure is introduced. The transmittance increases with increasing pitch of BMA. The results obtained using UV-VIS spectrophotometer with handmade sample holder.

Jan 1, 2015

By Li Ma, Shaoguo Chen, Gele Qing, Qihang Liu, Keng Wu

Olivine contains higher MgO element, which can be added into blast furnace burden to improve slag stability and fluidity. Effect of calcined olivine and untreated olivine on low silicon pellet production process and quality was studied in this paper. The results shows, calcined olivine has no effect on bursting temperature of green pellet, however the bursting temperature of green pellet will decrease with increase of untreated olivine ratio. Untreated olivine has slight effect on green pellet strength than calcined olivine while the ratio is higher than 2%. The compressive strength of low silicon pellet will increase first and decrease afterwards with increases of calcined olivine ratio under firing temperature of 1250°C, whereas, the changing sequence is reverse fired under 1280°C. The result of untreated olivine pellet compressive strength is same as calcined olivine pellet. However, the compressive strength and metallurgical property of calcined olivine pellet is slightly higher than that of untreated olivine pellet under same condition.

Jan 1, 2015

By Wei Lv, Xuewei Lv, Senwei Xuan, Chenguang Bai, Kai Tang

The contact angle between six iron ores and water were determined by the capillary pressure method with cyclohexane as the perfect wetting liquid. The factors influencing the contact angle were discussed, and a relationship between the content of oxy–hydroxides and the contact angle of iron ores was obtained. The results show that the ore F has the lowest contact angle but the ore D get the biggest, which are 32.09° and 78.16°, respectively. The volume fraction of oxy–hydroxides is linearly dependent on the contact angle. The contact angle decreased with increasing the volume fraction of Fe2O3*H2O.

Mar 1, 2017

By Zhang-Guang Gao, Ming-Mei Zhu, Rui-Rui Zhao, Chao Jiang

This paper focuses on the CaO-SiO2-FeO-MgO-MnO-P2O5 slag system that represents the major components of dephosphorization slag in BOF. Phosphorus distribution between 2CaOSiO2-3CaOP2O5 Solid Solution and Liquid Slag were analyzed by FactSage. The effects of slag content, basicity on the distribution ratio of P between the solid solution phase and the liquid phase (LP) and the percentage content of P in solid solution phase and liquid phase have been discussed. The results show that, with the increase of basicity, LP (wt%) decreases until the basicity reaches 1.9, then it turns to increase. LP (wt%) increases gradually with the increasing amount of FeO or P2O5.

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.