Search Documents

By Evan Jamieson

The conditions under which various iron(III) oxy-hydroxides phases precipitate from iron(III) chloride and sulfate solutions at ambient temperatures (<60°C) are reviewed. Many of these precipitates are slow settling and gelatinous but ultimately transform into other more stable or crystalline phases. The phase that forms depends upon the rate of precipitation and pH. A comparison has been made of the iron(III) oxides formed upon the neutralisation of various iron(III) solutions with caustic, slaked lime or slaked magnesia which provide different rates of neutralisation and slowly dissolving solids with localised high pH. Mössbauer spectra of ferrihydrites precipitated under these different conditions are compared and interpreted. Particular attention is paid to the settling rate and settled volume which is likely to relate to industrial thickener and filter performance. It is shown that in pure chloride solutions, poorly settling ferrihydrite is usually produced at 20oC regardless of the choice of base. However in sulfate solutions fast settling precipitates are produced using lime and magnesia but not with caustic. In mixed chloride/sulfate solutions, optimum settling rates occur when the molar ratio of [SO4]2to Fe3+ is about 1:1 and when the sulfate concentration is <0.20 M. It is proposed that ?dense amorphous basic iron sulfate? or well-ordered ferrihydrite is formed on slowly dissolving lime or magnesia surfaces. Implications for industrial liquors are considered.

Jan 1, 2003

By E. A. Chavarriaga, L. J. Jaramillo, O. J. Restrepo

"This paper presents the results of the manufacturing ceramic pigments with spinel structure, using methods of synthesis of low temperature. In this work we obtained spinel structures type by the methods of Self-combustion, Coprecipitation, Microemulsion, Gel citrate and Pechini. These methods become an attractive alternative to traditional method (ceramic method), since we can work at a lower temperature, reducing manufacturing costs, lower fuel consumption, less wear on equipment and other environmental and economic implications. Also it is possible to have control over features such as stoichiometry, morphology of the products, reaction times and structures. The products obtained by these routes will be used in the manufacture of ceramic pigments and characterized using different techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV-VIS spectrophotometry.IntroductionSpinels are ternary oxides AB204, where A and B are cations occupying tetrahedral and octahedral positions respectively. These oxides exhibit interesting electrical, magnetic and catalytic properties [1-4], depending on its nature, charging and intrinsic distribution of ions [5].The most widely used method to prepare spinels has been through solid state reaction, which consists of mixed oxides at high temperatures [6, 7]. In the last years, there have been a strong tendency to use chemical routes for the synthesis of crystalline ceramic particles at low temperatures [8,9]. Unconventional methods currently employed for the synthesis of complex oxides are Gel citrate method, Pechini, Spontaneous combustion, Microemulsion and Coprecipitation. Pechini method [10, 11], based on polymeric precursors, does not require high temperatures and allows stoichiometric control for greater reproducibility. This method involves the formation of a polymeric resin between a metal quelate and polyhydroxy acid of alcohol by polyestirification.Coprecipitation is important for many environmental problems related to water resources, including acid mine drainage, migration of radionuclides in waste repositories dirty, transport of contaminant metals in the industry, metal concentrations in aqueous systems and the technology of wastewater treatment. The coprecipitation process can vary in each case; the partition in the solid phase can be carried out by surface adsorption, ion exchange, surface precipitation, occlusion and formation of solid solution. The formation of solid solution is the result of structural incorporation of the marker in structural support sites resulting in a minor component in the solid solution with the host phase that has a very low solubility of pure solid [12]. Synthesis by gel citrate method allows the use of a route to obtain ceramic pigments from a very simple experimental system in which the stoichiometric control, the size and shape of the particles and the purity of the phases obtained can be controlled more accurately [13]."

Jan 1, 2012

By H. Dijkman

The PAQUES Bio Systems&apos; core technology, marketed under the name THIOPAQ®, consists of various high-rate biological processes for metal-sulfur-water systems, complemented with common solid/liquid and gas separation steps. Sulfur species are converted to sulfide, which is a valuable component as it can be used for metals reduction and precipitation. Selective recovery of valuable metals can be employed, leading to revenue from metal values. In this paper, biotechnological systems for the treatment of metal sulfate solutions and dilute SO, gases are described. These installations can be designed to either produce predominantly aqueous (NaHS) or gaseous (H2S) sulfide. The emphasis here is on hydrogen sulfide gas. The main case history discussed is the demonstration plant that ran on hydrogen gas at Kennecott Utah Copper. Three years of operating experience clearly show that sulfate reduction with hydrogen gas is a viable option. Furthermore, the selective recovery of copper from leach water with the hydrogen sulfide produced was shown to be very effective.

Jan 1, 1999

By Mingzhou Li, Lin Wu, Changren Tong, Fengli Yang, Shaohua Yang

"According to characteristics of Tm, Yb and Lu enriched oxides composition and problems in its traditional extraction separation process, the computer simulation of a optimized fuzzy extraction separation process, in which three products with high purity(>99.99%) could be obtained at same time, was carried out. Distributing Curves of every element in both organic and aqueous phases were worked out. Distribution rules of rare earth elements in every stage of the optimized extraction process were studied. The computation results of economical and technical index showed the consumption of the acid and base chemical reagents in the optimized process would be saved more than 30%.IntroductionFor the solvent extraction separation process of rare earths, countercurrent extraction process was widespread in the industrial practice. Normally, rare earth ions were extracted by the saponificated extractant and transferred into the organic phase, where the acidic extractant was saponificated by the base firstly. Then, the loaded rare earth ions were stripped from the organic phase into the aqueous phase by the acid. Therefore, the acid and the base were the main consumptions in the process, and the equilibrium acid of the stripped rare earth solution was one of the main pollution resources. Meanwhile, for the heavy rare earths, such as Tm, Yb and Lu, stripping was more difficult, and the equilibrium acidity of the stripped rare earth solution was higher, so the acid consumption increased greatly."

Jan 1, 2012

By Adam Powell, David Dussault

"Electric Field-Enhanced Smelting and Refining is a process for driving the reaction between carbon in hot metal and iron oxide in slag, for example, in a steelmaking reactor. This process involves inserting electrodes into the slag and metal phases, such that the overall reaction FeO + C -> Fe + CO is separated into two half-cell reactions: Fe2+ + 2e· -> Fe at the cathode in the slag, and C + O 2 • -> CO + 2e· at the anodic slag-metal interface. Without the electrodes, the reaction is very slow, but with electrodes, the additional surface area available to the ferrous ions for reduction accelerates the reaction even without any applied bias. When a bias is applied to the electrodes, the electric field across the slag further accelerates the overall reaction.With or without applied bias, the process is first-order in the ferrous ion concentration, and limited by ferrous ion transport to the cathode. To complicate matters, as the liquid iron is reduced at the cathode, the Mullins-Sekerka instability leads to formation of dendrite-like liquid iron fingers which grow into the slag. Because of this, the design of the cathode can have a significant effect on the overall process kinetics, and understanding of the dynamics of these fingers and of their effect on mass transfer is necessary for the intelligent design of the overall process and the cathode in particular.Toward this end, a detailed mesoscopic two-phase slag-metal model is presented here which describes multi component diffusion in the slag and fluid flow in both phases in the vicinity of the cathode. Diffusion in the slag is driven by chemical and electrical potentials. The phase boundary is modeled as a diffuse interface using a phase field approach. Because this electrochemical reaction occurs at high-temperature, the kinetics of charge transfer and adsorption through the double layer are fast relative to transport, permitting the use of simple linear reaction kinetics. This also eliminates the need to discretize the double layer, with the result that charge neutrality may be assumed everywhere in the domain. Introducing electric field dependence of the gradient potential and well height coefficients in the free energy function allows the model to capture electrocapillarity at the interface."

Jan 1, 2001

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 T. C. Tseng

Austenitization is a critical stage in heat treatment of steels. The available kinetic data in reference to various initial microstructures are very limited, particularly at high heating rates. In this study, integrated experimental and computational approaches have been conducted to quantify the progress of austenitization and the attained microstructure. In particular, the study is concentrated on cementite and carbide dissolution in two steel grades. Various computational methods are developed to facilitate the study: (l) an algorithm for direct determination of kinetics data as well as progress of transformation from high-rate dilatometer tests; and (2) a suite of mesoscale computational models for particle dissolution, elements diffusion, mechanics, thermodynamic and the resulting kinetics of transfonnation. Critical exprimentation is carried out using advanced techniques in microstructure characterization, chemical analysis, and Gleeble thermal-mechanical simulator on specimens of well-controlled initial microstructures. Keynotes: Cementite, Carbite, Dissolution, Steels, Austenitization

Jan 1, 2003

By S. de Vries, B. Wasmund, J. Metric, N. Voerrnann, S. Kasinger

Gulf Chemical & Metallurgical Corporation (GCMC) operates a circular DC electric smelting furnace to treat nickel and cobalt bearing residues at its plant in Freeport, Texas. The furnace, originally built by others, has experienced problems including runouts through the hearth and the lower sidewall. Hatch has designed several improvements to the furnace to alleviate these problems. The single anode at the centre of the hearth was replaced with a patented system of twelve air-cooled copper anodes evenly spaced around the furnace lower sidewall. The DC power supply comprises two transformers and two rectifiers operating in parallel. The water-cooling system on the bottom and lower sidewall shell plates was replaced with an air-cooling system using copper cooling fins. The existing row of water-cooled copper coolers in the metal bath zone was re-designed for greater heat removal capacity and better element joint sealing, and a new row of water-cooled copper coolers was added to cool both the alumina bath and freeboard zones. The existing water-cooled metal and alumina tapblocks were also re-designed for more robust cooling. A binding system was added to provide refractory compression that reduces the risk of liquid leaks. Finally, the furnace tilting frame was relocated to the top of the furnace where it is less likely to be damaged.

Jan 1, 2000

By Wellington Pereira Inácio, Frederico Muylaert Margem, Artur Camposo Pereira, Sergio Neves

"Natural fibers are currently gaining attention as reinforcement of polymer composites for uses in engineering parts for automobile and building construction. In spite of environmental, economical and societal advantages, the natural lignocellulosic fibers are not as uniform in their dimension and properties as compared to synthetic. In recent works it was found that the variation in strength could be correlate to the equivalent diameters for several lignocellulosic fibers including the sisal fibers. In the present work an investigation on a possible correlation of the equivalent diameter with changes in density and elastic modulus was carried out. Precise measurements of the equivalent diameter, conducted in a profile projector, were correlated with the density and the elastic modulus by means of the Weibull statistic analysis. The results showed that an inverse correlation with the diameter also applies for both the density and the elastic modulus with a high degree of precision. SEM observation of the sisal fiber in structure and fracture aspects strongly indicate that defects and microfibril participation could be responsible for the inverse correlation.IntroductionAccording to Kalia [1], cellulose-based fibers are currently being pushed owing to their ""green"" image. Contrary to synthetic glass fiber, extensively used in our modem technology, these lignocellulosic fibers are renewable and can be incinerated at the end of the material's lifetime without adding pollution in the atmosphere moreover, the amount of CO2 released during incineration process is negligible as compared to the corresponding amount taken up by the plant throughout its lifetime. Even if an industrial processing equivalent of C02 release is added, the lignocellulosic fiber is considered neutral with respect to the emission of gases responsible for the global warming [2]."

Jan 1, 2012

By Anurag Tripathi, J. K. Saha, S. K. Ajmani, J. B. Singh

"The quality of steel is a major concern in the metallurgical industry. The control of liquid steel temperature can enhance the level of cleanliness in steel. Ladle is one of the major vessels used to transfer liquid steel between different stations. The heat transfer phenomenon taking place in this vessel needs to be monitored for controlling the liquid steel temperature. A CFD model was developed for prediction of liquid steel temperature during complete process cycle of ladles in direct heats. The model was validated with liquid steel temperature measured at on-line purging station and tundish during teeming from one of the actual steel plant. The accuracy of model was 96 %. The results obtained show insignificant effect of slag thickness, tapping temperature and ladle life on liquid steel temperature in the ladle. However, the importance of initial refractory temperature was noticed. The CFD model developed in present work can generate the thermal history of liquid steel and refractory walls of any ladle at any stage.1. IntroductionThe control of liquid steel temperature is desired to achieve required steel quality. The low casting temperature is detrimental and may result in nozzle blockages due to premature solidification in the tundish. The phenomenon of heat losses taking place in ladles needs to be understood for prediction of liquid steel temperature. The assessment of thermal profile of liquid steel from BOF converter to caster can be done through consideration of heat losses at all points. Hlinka and Miller [1] showed that the ladle pouring temperature varies due to heat losses from molten steel into surrounding refractory layers. The phenomenon of thermal stratification was numerically simulated by Ilegbusi and Szekeley [2]. The effects of slag cover on heat loss and liquid steel flow in ladle before and during teeming to a continuous casting tundish was numerically simulated by Chakraborty and Sahai [3]. Investigators also developed some simple models to predict the steel temperature for some of the processes taking place in ladles [4-9].The present work is an effort to generate the full information about the temperature drop taking place in any ladle throughout its process cycle. This information can be used to predict liquid steel temperature and to take decisions to minimize heat losses."

Jan 1, 2012

By Issa S. AI-Kharusy

Oxidation/reduction (REDOX) alloy media, as used in wastewater treatment, is founded on the exchange of electrons. Because of this electron exchange, many contaminants are converted to harmless components which require no further treatment. Other types of contaminants are removed from the waste stream by electrochemically bonding to the alloy medium. This paper discusses the REDOX reactions, the role of the alloy medium in various treatment processes, and describes specific applications of REDOX alloy media for the removal and minimization of waste. The characteristics and handling of spent treatment media is also reviewed as a further consideration in waste minimization.

Jan 1, 1996

By Rumen Markov, Lubomir Kuzev

"The treatment technologies for municipal solid waste (MSW) are effective mainly for components sized over 40 – 50 mm. This fraction is separated by screening in the beginning of the process. Usually the undersized product is deposited without additional treatment. Its quantity is variable from several up to 30 – 40 % of the total MSW. Both oversized and undersized fractions are formed by all types of primary matter. Adapted technologies from mineral processing will provide a suitable technology for treatment of MSW under 40 – 50 mm. The MSW content depends on the geographical location, the degree of urbanization and other factors. The methods can be applied for separations of different components suitable for recycling or other utilization are: • Separation by density; • Separation in thin liquid layer; • Selective grinding and screening; • Flotation, etc. Introduction Municipal solid waste (MSW) represents an integral part of public urbanization. However, there are some drawbacks stemming from MSW, in regard to its collection, transport and elimination. Different approaches exits worldwide for tackling the problems arising from MSW. For a short period of time, the attitude towards MSW has evolved in several levels, each further level being characterized by higher percentage of utilization of MSW components. Thus, the bottom line has been shifted from safety storage towards processing that includes recycling and maximal utilization of MSW components. Technologic processes applied for treatment of MSW have a common feature – that the fine components, having sizes under 20 mm, 30 mm, 40 mm, or 50 mm are excluded from treatment process trough screening, and in most cases diverted without any additional treatment to preliminary prepared storage sites. MSW in Sofia – current situation The amount of MSW collected daily in Sofia as around 1000 t/24 h. It is stored or baled. Baling is a spare alternative of storage, since baling insures only temporal keeping of MSW, till the building of suitable storage site where the bales will be transported and buried. The morphologic composition of MSW in Sofia has been determined several times at different time intervals, from some Bulgarian organizations as well as from the Japanese organization JICA. So far, however, there is still a lack of enough systematical and comprehensive study. Generalized results from the studies on the MSW components, as well as some important parameters are given in Table 1."

Jan 1, 2008

By Carla Lupi, Mauro Pasquali

"Photographic technology is based on light sensitivity of silver halides that, because of silver properties, are capable of forming photographic images. Photographic laboratories and hospital departments because of digital photographic systems less use this technology today. Nevertheless recovery of silver is still advantageous because environmental problems related to Ag ions danger to biological system. Many processes have been studied to treat silver containing photographic bath: cementation, chemical precipitation and electrowinning. In this work, after preliminary voltammetric tests, a batch electrometallurgical process has been studied to completely deplete the silver containing photographic fixing baths. The effect, of silver concentration in the electrolyte, varying over the range 0,2-1 g/L, bath stirring and current density ranging from 10 to 500 A/m2 on process yield and deposit quality, has been investigated. Introduction Photographic wastes, electronic scrap and spent catalysts constitute the main sources of materials for silver recycling. Among those silver secondary sources, the photographic discharged material could be still important and useful, even if photographic laboratories and hospital departments, because of digital photographic systems, less use photographic technology. Several processes have been developped in order to recover silver used in the field of photography from both photographic solutions and scrap film paper[1-5]. Fixing solutions are very complex baths but, because of silver position in the electromotive series, electrolysis could represent an advantageous method for silver recovery. Electrolysis produces high purity silver without generating new pollutants, while the fixer can be reused: obviously it is necessary to purge off a portion of this solution in order to avoid the excessive build up of other deleterious compounds into solution. A tested recovery method was constituted by the dissolution of silver from X-ray films with concentrated nitric acid. Internal electrolysis and external electrolysis methods were carried out using a steel electrode as cathode and a copper electrode as anode [6]. Silver recovery from photographic chemical solutions has been also performed in a special cell [7]: the solution is supplied to the bottom of a non-agitated cell having a vertically elongated form and including a central anode enclosed by a cathode. An other study discloses the use of an electrolytic cell comprising at least one anodic compartment and one cathodic compartment: the solution is treated in the cathodic compartment and then recycled in the anodic one [8]. A more recent work proposes the use of zirconium cathode for the recovery of silver from photographic fixing solution [9]: studies carried out by cyclic voltammetry showed that about 98% of total Ag can be recovered with an electrical efficiency close to 92%."

Jan 1, 2008

By Xuewei Lv, Maojun Zhou, Xiaobo Huang, Rende Zhang

"The characterization of the surface roughness of the mineral particles is of vital importance for the studies of the mineral processing. In this study, an evaluation of the roughness of the iron ore particles, with the measurements of size distribution and the measurements of specific surface area with the liquid nitrogen absorption, was developed. The main theory of this method is the fact that the roughness of the particle influences the specific surface area apparently. The specific surface area of the particles can be measured with the laser diffraction method and the liquid nitrogen absorption method. The influence of the surface roughness of the particle can be measured with the nitrogen absorption and cannot be measured with the laser diffraction. Therefore, the roughness can be got by comparing the specific surface area with two measurement methods.IntroductionThe characterization of the surface roughness of the mineral particles is of vital importance for the studies of the mineral processing. There are three main methods for measuring the size distribution of mineral particles: sieving, laser diffraction, and sedimentationl). Many techniques involve sedimentation such as the Horiba2, 3) and the Cyclo-sizer1). In the mineral industry, size distribution is usually determined by sieving because it can be carried out accurately for all particle sizes larger than 45 . The preferred method to obtain the size distribution of finer particles is laser diffractometry. The technique has several advantages: it produces measurements in a few minutes with considerably less labor compared with the cyclo-sizer and for a range of sizes considerably wider in comparison with the sedigraph4). The equivalent-sphere size distribution reported by laser diffractometry is valid for metallurgical calculations and can be routinely used in mineral processing plants. The surface area of the particles can be measured by the BET method of nitrogen adsorption, or it can be calculated from the size distribution. However, the latter calculation requires the size distribution to be accurately known across the whole size range, and assumptions have to be made about the shapes and surface roughness of the particles and presence or absence of pores (see below). The BET method is based on the physical adsorption of gas over the whole exposed surface area and measures the surface area stemming from the roughness and open pores on the surface of the particle5). The calculation of the surface area from the size distribution is usually based on the assumption that all the particles are smooth spheres, without considering the shape and/or roughness of the particles. Determining the surface roughness of the particle with these methods, is the objective of this study."

Jan 1, 2012

By Masatsugu Morimitsu, Tian Zhang

"This paper presents a novel anode for oxygen evolution in acidic aqueous solutions to produce non-ferrous metals by electrowinning. The method to prepare the anode was thermal decomposition of a precursor solution, and the obtained anode consisted of Ru02-based oxide catalytic layers formed on a titanium substrate, in which the catalytic layer contains nano-oxide particles as the active component. The oxygen evolution potential was lower than amorphous lr02-Ta20s coated titanium anodes so that the cell voltage of electrowinning was further reduced with the amorphous Ru02-based electrode.IntroductionElectrowinning (EW) is used to produce high purity of non-ferrous metals, and the primary metal production of copper, zinc, nickel, and cobalt by EW consumes huge electric energy worldwide, which tends to increase with increasing demand of such metals. The reduction of electric energy consumption is a significant issue for electrowinning industry, which means that the cell voltage reduction is needed to realize more energy-efficient EW processes. Another issue is also indicated from environmental perspectives; i.e., an improvement in EW plant environment by eliminating hazardous byproducts and wastes. Such byproducts and wastes include lead oxide, manganese oxide, and acid mist.We have been developing the anodes for energy-efficient and environmentally friendly electrowinning processes [ 1-11]. The development has been successfully done with the invention of the smart anode, MSA TM (Morimitsu Smart Anode) [ 1-5], which has low polarization for the main reaction and high polarization for the side reaction, in which the main reaction is oxygen or chlorine evolution, while the side reaction is the anodic deposition of each or both of lead oxide, manganese oxide, and cobalt oxide. The anode consists of a valve metal substrate coated with amorphous or less crystalline oxide catalytic layers. One of the typical examples of such oxides is amorphous lr02-Ta20s, and the substrate is normally titanium plate or mesh. The most important point of the oxide is that the amorphization or less crystallinity induce the increase in the active surface area only to the main reaction, not to the side reaction, thereby the polarization of the main reaction being reduced.In this paper, we present the smart anode consisting of RuO2-based catalyst formed on titanium substrates for oxygen evolution in electrowinning. The preparation, characterization, and polarization behaviors of the anodes are shown, and the cell voltage data for zinc or copper electrowinning using the anodes are also presented."

Jan 1, 2012

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Maria Salazar-Villalpando, Todd H. Gardner

"Efficient utilization of CO2 can help to decrease global warming. Methane reforming using carbon dioxide has been of interest for many years, but recently that interest has experienced a rapid increase for both environmental and commercial reasons. The use of CO2 provides a source of clean oxygen, which eliminates the need for costly oxygen separation plants. The product of dry reforming is useful syn-gas, which can be used to generate electrical power in a SOFC or in the production of synthetic fuels (hydrocarbons and alcohols). Hexaaluminate catalysts prepared at NETL may represent a product that can be utilized for the conversion of CO2 to syn-gas. In this work, transition metals dispersed in barium hexaaluminate have shown to be promising new catalysts for dry methane reforming. In this investigation, a series of BaNixAl12-yO19-d catalysts with varying Ni content were prepared by co-precipitation followed by calcination at 1400°C. CO2 reduction by dry methane reforming was carried out to determine catalyst performance as a function of temperature and carbon formation was also quantified after the reforming tests. Results of catalysts characterization, dispersion and surface area, were correlated to catalytic performance.IntroductionEfficient utilization of CO2 can help to decrease global warming. Methane reforming using carbon dioxide has been of interest for many years, but recently that interest has experienced a rapid increase for both environmental and commercial reasons. The use of CO2 provides a source of clean oxygen, which eliminates the need for costly oxygen separation plants. The product of dry reforming is useful syn-gas, which can be used to generate electrical power in a SOFC or in the production of synthetic fuels (hydrocarbons and alcohols). The dry reforming reaction has been known for a long time. Recent publications have reported studies over several catalysts. For example, the CO2 reforming of CH4 over mesoporous nanocrystalline zirconium powders (ZrO2–3%M2Ox; M: Ce, La and K) at 700ºC have shown methane conversion up to 60% (1). Similarly, the effect of Ni content (1–12 wt%) on the surface and catalytic behavior of bimetallic PtNi catalysts supported on ZSM-5 for reforming of methane with CO2 has been studied and report shows a maximum conversion of 16% and catalyst deactivation was observed during the first hour of time on stream (2). In another report, (3) Ni/a-Al2O3 catalyst was tested for syn-gas generation at 750ºC. The maximum methane conversion was 25%."

Jan 1, 2008

By Gaifeng Xue, Lei Zhang, Xia Liu, Lina Wang, Pu Liu, Benquan Fu

"Experiments were conducted to investigate the behavior of the integrated process with a three-dimensional electrode reactor combined with Fenton process for coking wastewater treatment. Effects of initial pH value, reaction time, H20 2 dosage, Fe2+ dosage on Total organic carbon (f OC) removal rate were investigated. The kinetics of degradation of TOC from coking wastewater by three-dimensional fluid bed electrode reactor combined with Fenton process was also studied. Experimental results shows that three-dimensional fluid bed electrode reactor combined with Fenton process had better synergic effect, average 17.4% TOC removal rate was improved within an hour. It was found that TOC degradation in coking wastewater followed a pseudo-first-order reaction kinetic model. The optimum degradation efficiencies of TOC were up to 60% as pH3.4, 3.5 mM ofFe2+ andl.2-1.8ml/L H20 2 in 90min reaction period. Furthermore, the integrated process showed a rapid reaction performance at a low temperature within a short reaction time and remained high efficiencies for TOC removal. Overall, the integrated process was proved feasible for coking wastewater treatment in practical applications.IntroductionCoking wastewater is generated from coal coking, coal gas purification, and by-product recovery processes of coking, which is composed of phenolic compounds, heterocyclic compounds, polycyclic aromatic hydrocarbons, ammonia, cyanide, polycyclic nitrogen-containing aromatics, acyclic compounds, etc. Most of these constituents are refractory, poor biodegradability, toxic and carcinogenic['-31. Currently, coking wastewater is usually treated by different forms of A/O biological nitrogen removal process as the primary treatment process, but the aforementioned processes are not efficient enough to meet the requirements from the National Discharge Standard in China (GB13456-1992). According to the continuous requirement on improving environmental protection for coking industry (revised 2008), increasing wastewater utilization ratio and reducing discharge of effluent in the coke industry has to be implemented for cleaner production and sustainable development. Therefore, advanced technologies need to be developed to treat coking wastewater and reutilize the product as industrial cooling water, which would be one of the best choices to achieve zero discharge of wastewater and reduce water consumption per ton of steel [4-51 . In this study, three-dimensional fluidized bed electrode reactor combined with Fenton process was adopted to advanced treatment of coking wastewater, and the effects of operating conditions, including H2O 2 dosage, Fe2+ dosage, initial pH, and reaction time on TOC removal rate, were investigated. Meantime, study of kinetics of reaction was estimated."

Jan 1, 2013

By Richard Jack De Klerk

The standard industrial method of arsenic removal from acidic aqueous processing effluents involves coprecipitation of arsenic with ferric iron (Fe/As>3) by lime neutralization in continuous circuits. To better understand current industrial practice, continuous circuit coprecipitation experiments were performed to identify industrially relevant process parameters and co-ion solutes that contribute to improved arsenic removal and retention. The coprecipitated solids were subjected to accelerated ageing at 20°, 40° & 70°C and arsenic behavior was monitored and modeled. Staging and the presence of calcium ions were found to have the most significant impact on arsenic retention. In this paper the techniques used and major results obtained are discussed.

Jan 1, 2008

By L. Béjar-Gómez

The aim of this research work is to study and characterize precipitates in structural microalloyed steel by transmission electron microscopy and analysis by high resolution (HRTEM). Microalloyed steel with titanium was produced by casting in an electrical induction oven of 25 Kg. capacity. Carbon content in steel was less than 0.1 % and titanium content of 0.04%. Steel was processed thermomechanically; reheated to 1250ºC and hot rolled on a laboratory mill to a 13.0 mm thick plate with a finish rolling temperature of 900ºC and thickness reduction of 80%. Analysis by High Resolution Transmission Electron Microscopy (HRTEM) identified precipitates in the steel; type and morphology. Energy Dispersive Spectroscopy (EDS) analysis was applied to obtain the chemical composition of precipitates and the matrix. STEM-EDS analysis was also applied to obtain the element profile of precipitates. The results showed the presence of carbonitride precipitates of titanium, Ti (CN), with a circular morphology and size of 10 nm and less.

Jan 1, 2006