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By Yousef Mohassab, Manoranjan Misra, Monalisa Panda, Eman Wahbah

This work studies the removal of arsenic (V), arsenate, and arsenic (III), arsenite, from aqueous solution using calcined Quintinite-3T. The two adsorbents Quintinite-3T was prepared, calcined at different temperatures, and characterized by XRD, BET, and SEM. The surface area of the calcined Quintinite-3T was 193.4 m2/g. The particles size ranged from 12 to 56 nm for the uncalcined Quintinite-3T and from 24 to 42 nm for the calcined Quintinite-3T. Kinetic analysis, adsorption isotherm, and factors affecting the adsorption were investigated. Calcined Quintinite- 3T retained As(v) and did not release it back to water even after an entire month.

Jan 1, 2016

By Luciano E. Ramírez, Jesús L. Valenzuela, José R. Parga

"An innovative process for removing copper cyanide complexes including silver and zinc from cyanidation circuits has been developed. The technology was based on the inducing the nucleated precipitation of copper and silver in a tube serpentine reactor, using sodium sulfide as the precipitate and sulfuric acid as pH control. The results showed that pH had a great effect on copper cyanide removal efficiency and the optimum pH was about 3 to 3.5. At this pH value copper cyanide removal efficiency could be achieved above 97 and 99 % ,when influent copper concentration ions were 650 and 900 ppm respectively. In this process (sulphidizaton-acidification-recycle-thickening), the cyanide associated with the copper cyanide complexes is released as HCN gas under weakly acidic conditions, allowing it to be recycled back to the cyanidation process as free cyanide. This system was successfully commercial applied at Minera William in Mexico.IntroductionThe recovery of gold and silver from minerals and concentrates with cyanide is an important hydrometallurgical process, which has been studied for more than 124 years. Patented by MacArthur in 1888 [1], the process relies on the fact that gold dissolves in aerated cyanide solutions to produce the gold cyanide complex. The stoichiometry by wich this reaction occurs is known as the Elsner equation as shown here. Silver is accomplished in the same fashion."

Jan 1, 2012

By Henrique Kahn

The Anitapolis alkaline massif in southern Brazil underlies a sub circular area of 6 km2. Bore-hole data show a concentric rock distribution, with mafic rocks in the central part and felsic rocks in the border zone. The rocks are covered by talus and weathered material, 30 m thick on average, and very inhomogeneous in composition. Phosphate mineralization associated mainly with two levels of the weathering mantle and with fresh rocks. A preliminary ore-type classification was based on distribution of apatite, feldspar, vermiculite, biotite-phiogopite, calcite, pyroxene, amphibole and analcime, determined by semiquantitative diffraction method. Technological tests performed on eluvial ore samples from three adits resulted in a subdivision of ore-types based on the difference in behavior due to mineral characteristics during mineral pr

Jan 1, 1991

By Hui Zhang

The leaching behavior of palladium powder in aqueous solutions containing NaCI or N'H4Cl was investigated. Cupric ion was used as an oxidant for the dissolution reaction. The effect of a number of leaching parameters such as temperature, concentration, stirring speed and surface area on the leaching rate was studied. The leaching system containing chloride and cupric ion was found to be very effective for the dissolution of metallic palladium. Based on the experimental results the overall leaching rate was believed to be controlled by a chemical reaction step. The dissolution rate of palladium was found to be first order with respect to the concentration of cupric ion and second order with respect to the concentration of chloride.

Jan 1, 1996

By Dae Jin Ha

Sticking phenomenon occurring during hot rolling of two STS 430JlL ferritic stainless steels was analyzed by hot-rolling simulation tests. The sticking started from the initial nucleation stage in which the rolled materials were stuck onto the roll specimen surface, proceeded to the growth stage in which stuck fragments grew further, and reached the saturation stage. The modified 430JlL steel had a smaller number of sticking nucleation sites and slower growth rate than the conventional 430JlL steel because of higher high temperature hardness, thereby leading to less serious sticking. When the simulation test was conducted at 1070 °c, Cr oxides were formed on the surface of the rolled materials, and thus the sticking was drastically reduced because of the increased surface hardness of the rolled materials. In order to prevent the sticking, high-temperature properties of the rolled materials should be enhanced when rolled at 900°C or 1000 °C, and rolling conditions and alloying compositions, under which the oxide formation was promoted, were more important than high-temperature properties when rolled at higher temperatures than 1000 oC.

Jan 1, 2008

By N. Coone

By exploiting the results of solidification modelling foundries can enhance the quality and reduce the cost of their casting processes. However not enough information exists on the thermal boundary conditions, which control the transfer of thermal energy stored in liquid metal to the mould via the metal/mould interface during solidification. This is quantified by the heat transfer coefficient (h.t.c.). An experimental and numerical study was carried out to find the magnitude and variation of the h.t.c. in cylindrical castings during the solidification of grey cast iron in green sand moulds. The h.t.c. values were calculated using a time marching solution to the inverse heat conduction problem. The variation of h.t.c. with metallostatic head was analysed. There is a wide scatter in green sand thermal properties due to the large number of variables involved in mould manufacture including green sand compaction and water content. The sensitivity of the calculation to uncertainties in the thermophysical properties of the green sand was evaluated. Keywords: Heat transfer coefficient, grey cast iron, sand moulds. inverse technique

Jan 1, 2003

By Shadia J. Ikhmayies

CdSxTe1-x and CdS1-yTey solid solutions are usually formed in the interfacial region in the CdS/CdT thin film solar cells during the deposition of the CdTe layer and/or the processing steps of the device. It is well known that CdCl2 heat treatment encourages the formation of the CdSxTe1-x alloy which improves the solar cell performance. In this work, indium doped CdS1- yTey thin films are produced by first producing CdS:In thin films by the spray pyrolysis (SP) technique on glass substrates, then annealing the films in nitrogen atmosphere in the presence of elemental tellurium. The films are characterized by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and transmittance measurements. The transmittance is used to deduce the optical parameters such as; the extinction coefficient, refractive index, besides to the real and imaginary parts of the dielectric constant. The dispersion parameters such as Eo (single-oscillator energy) and Ed (dispersive energy) of the deposited films are also estimated and discussed.

Jan 1, 2015

By Mikiya Tanaka, Mikio Kobayashi, Mansour A. S. A1Ghamdi, Kenji Tatsumi, Yukinori Saiki, Hirotaka Senba

"In order to recover nickel ion in a spent electroless nickel - phosphorus alloy plating bath and, at the same time, to remove impurities such as iron and zinc, the applicability of solvent extraction with LlX84I as the extractant has been investigated using actual spent solution. Although the extraction efficiency of nickel from the spent solution is considerably lower than that from the nickel sulfate-nitrate solution, nickel in the spent solution is selectively extracted with high efficiency at the pH of 6 - 7. The extracted nickel is effectively stripped by sulfuric acid at a pH of less .than· 3. On the basis of these results, a· flowsheet for recovering nickel from the spent solution is proposed Chemical equilibrium calculations of the spent solution has shown that the complex formations of nickel with anions such as lactate and phosphonate ions become predominant in the pH range between 2 and 6. This results in the depression of nickel extraction efficiency from the spent solution as compared with that from the .nickel sulfate-nitrate solution. By combining these aqueous equilibrium calculations with the· extraction model considering the extraction stoichiometry and the aggregation of the extractant in the organic phase, the extraction behavior of nickel is quantitatively predicted.IntroductionElectroless plating is indispensable for the recent advanced industries such as the electronic and mechanical industries. Electroless plating baths are repeatedly used by supplying the metal salts; however, the accumulation of the counter anions of the metal ions, the components formed by the oxidation of the reducing reagents in the plating baths, and the metal ions as impurities dissolved from the surface of the objective materials degrades the· quality of the plating. Thus, the baths are finally treated by a precipitation method to form a large amount of metal sludge, which is disposed in dumping sites. Therefore, from the standpoints of environmental protection and resource preservation, it is highly desired to establish a recycling process of the plating baths with minimum emission. Solvent extraction seems to be one of the 'suitable methods to recover metals from the spent electroless plating baths, because the concentration of the metal ion in the baths is relatively high, which is advantageous to solvent extraction as compared with the ion-exchange and adsorption methods. Some studies about the application of solvent extraction have already been carried out using simulated spe11t electroless plating baths [1-3]."

Jan 1, 2000

By B. Q. Li, R. A. Mirshams

"A numerical algorithm is described for the simultaneous prediction of the thermomechanical behavior of the materials and microstructure evolption during metal forging. The numerical development is based on the finite element solution of the thermoviscoplastic deformation of metals coupled with the internal state variable model describing the microstructure evolution involving work hardening, recovery, recrystallization and grain size distribution. The finite element code for rigid viscoplastic deformation is developed based on the modification of the existing code for the thermal and fluid flow calculations. The code is tested against and compares well with the results reported in literature. The procedures for the integration of the · rnicrostructure model into the macro finite element model are described. Results are presented showing the characteristics of materials dynamics and mechanical deformation during simple metal forging processes.IntroductionIn industrial deformation processes such as hot rolling and forging, the workpiece undergoes both macroscopic plastic deformations and microstructural evolution. A computer model that allows to predict both materials dynamics and macroscopic deformation is obviously more useful for both fundamental understanding and deformation process optimization. For some industrial applications, especially those involving novel, light and high strength materials, such an integrated model is critical in that both materials and thermomechanical 'behavior during forging must be carefully controlled to obtain the products that meet the desired strength requirement [I]."

Jan 1, 2000

By D. J. Chaiko

Certain radionuclide ions (e.g., TcO4) exhibit unusually strong Affinities toward the polymer-rich phase in aqueous biphase systems generated by combinations of salt solutions with polymers such as poly(ethylene glycol) (PEG) and poly(propylene glycol) (PPG). Thus, aqueous. polymer ,phases could potentially be used to selectively extract these ions during pretreatment of radioactive tank wastes at Hanford. To help develop a fundamental understanding of the interactions between various ions and polymers in aqueous solution, interaction enthalpies between sodium -perrhenate and a random copolymer of PEG and PPG (UCON-50) were measured by microcalorimetric titration. An entropy compensation effect was observed in this system in which changes in enthalpic interactions were balanced by entropy changes such that the interaction free energy remained constant and approximately equal to zero.

Jan 1, 1999

By M. Misra, J. Nanor

The precipitation and removal of arsenic from process waters can be accomplished with addition of lanthanum chloride alone or in conjunction with ferric sulfate. The long term stability of these corresponding precipitated compounds is critical from the disposal stand-point. In this paper the characterization of ferric, lanthanum and lanthanum-ferric arsenate compounds formed at room temperature in acidic and alkaline pH is presented. The characterization techniques used included zeta potential, XRD and SEM. Zeta potential measurements of ferric and lanthanum hydroxides in the presence of arsenate indicate that oxyanions of arsenate are chemically adsorbed onto the positively charged surfaces of these hydroxides. In alkaline pH there is desorption of arsenate species from the ferric hydroxide surface, hence the product is thought to be unstable. On the contrary, lanthanum arsenate is stable in alkaline pH. XRD patterns show that the ferric arsenate formed in acidic and alkaline pH is amorphous, whereas lanthanum arsenate and lanthanum-ferric arsenate formed in acidic and alkaline pH are crystalline.

Jan 1, 1999

By J. S. Becker

Technology developed and first implemented in the United Kingdom enables very low grade aluminum scraps containing oils, organics, plastics and ferrous metals to be directly charged, without pretreatment, into a unique melting furnace. The system has been in full scale production for over three years. The oxy-fuel-based furnace design incorporates internal afterburning in the furnace's hot zone, producing excellent thermal efficiency and very low emissions. The furnace is inherently low in NOx. This paper will provide both theoretical background and extensive operating results for this new melting concept. Applications describing both purpose built new furnaces and retrofits of existing reverberatory furnaces will be presented. Extensive operating emissions data will be presented.

Jan 1, 1996

By Chunyang Guan, Jilai Xue, Jun Zhu, Qiaochu Liu

"Al-Sc Alloys have showed many advanced properties for a wide range of industrial application, which is usually produced using thermal reduction process. This work is aimed to develop an electrochemical process to make Al-Sc alloy using industrial Hall aluminum reduction cells. The experiments have been carried out in a lab cell where NaF/AlF3-Al2O3-LiF as electrolyte, Sc2O3 as raw material, and liquid aluminum as cathode were used at operating temperature of 950 °C. The resulting Al contained 0.2 - 0.5 wt.% Sc that is the common range in its content for advanced applications. However, a small fraction of Sc was found from thermal reduction at Al melts interface. SEM-EDS and ICP-AES analysis showed a uniformed distribution of Sc at varying locations of the Al-Sc alloy sample. In addition, a higher Sc content in Al-Sc alloy can be obtained with introducing ultrasound through the cathode than that without it.IntroductionIn recent years, scandium has been investigated as an alloying element for aluminum alloys. With addition of a small amount of Sc, Al alloys can improve the strength, weld ability, resistance to re-crystallization and corrosion resistance [1-3]. Due to their advanced properties and potential applications, the demand for Al-Sc alloys will increase in the future. However, the difficulties in reduction technologies and the high costs in production process may limit their expansion in application areas.The current major method of producing Al-Sc alloys is to mix Sc into Al by melting Al-Sc master alloy. This alloying process has several technical problems, such as easy segregating and heavy burning loss, etc. The price of Sc metal or starting material is also high, so the mixing process is an expensive alloying method. Molten salt electrolysis is alternative method to prepare RE metal and RE alloys [4, 5]. It also can reduce the segregation of alloying elements. Sc2O3 is an ideal material as raw material with low price and decomposition voltage. Some work has proved that Al-Sc alloys can be obtained by electrolysis Sc2O3 directly in cryolite [6-8], or CaCl2 molten salt [9]."

Jan 1, 2012

By W. K. Connor, O&apos

The U.S. Bureau of Mines, in cooperation with the Idaho National Engineering Laboratory (INEL), conducted over 30 hours of melting tests to vitrify simulated low-level radioactive wastes from the INEL Radioactive Waste Management Complex (RWMC). Five separate waste compositions were investigated, each consisting of noncontarninated soil from the RWMC and surrogate materials used to simulate the actual buried wastes. The RWMC soil and five waste compositions were melted in a 50-lb, single-phase electric arc furnace with a water-cooled shell. These tests were conducted to determine melting parameters in preparation for a large-scale melting campaign to be conducted in the Bureau's 1-metric ton (mt), water-cooled-wall, 3-phase electric arc fumace. Bulk chemical composition was determined for each of the feed materials and for the slag, metal, fume solids, and offgas furnace products, and distributions were calculated for the key elements. The material balance for the furnace operation indicates that from 63 to 84 pct of the feed reported to the slag. Cerium, used as the surrogate for the radionuclides in the wastes, demonstrated an extremely strong affinity for the slag product. Although slag temperatures as low as 1250° C were recorded when melting the RWMC soil, temperatures in excess of 1600° C were necessary to achieve the fluidity required for a successful slag tap.

Jan 1, 1994

By Wayne Bell, Matthew Andriese, Shuqian Xie, Jiann-Yang Hwang, Zhiwei Peng

"Pyrolyzed carbons are generally known as good microwave absorbers and their dielectric properties still remain to be fully explored. In the present study the dielectric properties and dielectric polarization-relaxation phenomenon of a typical activated carbon was investigated. The experimental results indicate the complex permittivity is highly dependent on temperature and frequency. The decrease of permittivity with increasing temperature from room temperature to ~100 °C is probably ascribed to the release of the water vapor adsorbed on the surface of activated carbon, and the variations of permittivity with temperatures between 100 °C and 450 °C in the frequency range of 300 MHz to 3000 MHz are mainly attributed to the decreased relaxation time of dielectric polarization.IntroductionPyrolyzed carbons have been identified as excellent microwave absorbers owing to their high dielectric and electrical loss under microwave irradiations. Among them, activated carbon continues to attract more and more attention from researchers. Due to its special physical properties, the production, modification and regeneration of activated carbon with the assistance of microwave have been widely studied over the last few decades [1-6]. However, only few attempts have been applied to explore the dielectric properties of such materials due to the complexity and variability of their organic precursors and activation processes [7,8]. In order to shed a light on this problem, a typical sample, Norit® A Supra USP powdered activated carbon, was adopted to perform dielectric characterization, which may provide useful information for its wide application in the fields of purification, energy (hydrogen) storage and so on."

Jan 1, 2011

By Jeong-Soo, Joon Soo Kim, Rajesh Kumar, Sohn, Jin-Young Lee

"Liquid-liquid extraction (LLE) studies of tetravalent platinum from acidic chloride solutions have been carried out with Alamine 336 as an extractant diluted in kerosene. The title metal shows the inverse behavior at higher acid concentrations. Plot of log D vs. log [Acid], mol.L-1 gave a straight line with a negative slope of 0.8±0.03 indicating the exchange of one mole of hydrogen ions for every mole of platinum(IV) extracted into the organic phase. Extraction of platinum(IV) increases with increase of extractant concentration. The plot of log D vs. log [Extractant], mol.L-1 is linear with slope 1±0.3, indicating the association of one mole of extractant with the extracted metal species. The plot between metal distributions to aqueous to organic phases is 1.3±0.01; it indicates monomeric species was formed in organic phase. Stripping of metal from the loaded organic (LO) with mineral acids such as hydrochloric, sulphuric, nitric acids and bases like ammonia, hydrogen peroxide and sodium hydroxide are studied. The results indicated that hydrochloric acid and sodium hydroxide are the better stripping agents when compared with other acids and bases. Increase of temperature decreases the percentage extraction of metal indicating the process is endothermic. Regeneration and recycling capacity of Alamine 336 and extraction behavior of associated elements such as aluminium(III), magnesium(II), cobalt(II), iron(III) and nickel(II) were studied.IntroductionThe demand for platinum group metals (PGM’s) has risen in the last five years expected to keep in rising. Right now, the demand is already beyond the supply. The primary use of PGM’s today is in the automotive industry. Catalytic converters used in the PGM’s process to reduce greenhouse gases. Because of the current demand to reduce the green house effect the expected need for platinum is here stay. Country’s now advancing in the use of car production also are phasing increasing the needs for this metal. Chemical processing also use it, too. These industries account for more than 50% of all platinum production. Jewelry is other primary use of this precious metal whose value is much greater than gold. Other uses include computer data storage, scientific developments, fuel cell technology and in the glass manufacturing processes."

Jan 1, 2008

By Qian Xu, Guangshi Li, Xionggang Lu, Xingli Zou, Hongwei Cheng, Cong Xu, Changyuan Lu

The roasting of nickel-bearing sulfides is a complex but important process which has not been adequately characterized. Combination of X-ray diffraction and scanning electron microscopy has been proved to be useful for such experiments. The leaching results of nickel, copper, iron and cobalt was analyzed by ICP methods. Process possibility of polymetallic sulfide concentrates through a three-step procedure (oxidation roasting - chlorination - water leaching) was suggested. Ammonium chloride could react with nickel/copper oxides to produce intermediate complexes. At the temperature range of 280~340 oC, these complexes further decomposed to the corresponding simple chlorides. Roasting sulfide concentrate using NH4Cl is effective for complex ores.

Jan 1, 2016

By James O'Brien, Lyman Frost, Grant Hawkes, S. Elangovan, Manohar Sohal, J. S. Herring, Joseph Hartvigsen, Carl Stoots

"Pressing environmental and energy security concerns have brought much needed attention to economic production of hydrogen as the secondary energy carrier for non-electrical markets as well as to meet increasing demand for crude upgrading and desulfurization. While steam reforming of natural gas is currently the dominant method of hydrogen production, it is depleting a valuable fossil fuel while emitting green house gases. Thus, in the long run, efficient, environmentally friendly, and economic means of hydrogen production using nuclear and renewable energy needs to be developed. High temperature electrolysis using solid oxide electrolyte cells is an exceptionally efficient means of generation of high purity hydrogen. It is also capable of directly converting steam and CO2 into synthesis gas. This co-electrolysis process enables conversion of CO2 recovered from concentrated industrial sources into a feedstock for synthetic fuels production. Use of CO2 provides a means of storing hydrogen in a concentrated and convenient form – a hydrocarbon. This is also an effective storage medium for intermittent renewable energy sources such as wind and solar.Ceramatec, Inc and the Idaho National Laboratory are applying solid oxide fuel cell technology to the production of synthesis gas by high temperature co-electrolysis of steam and carbon dioxide. This technology utilizes solid oxide fuel cell stacks to electrochemically remove oxygen from steam and CO2, leaving a clean stream of hydrogen and carbon monoxide suitable for fuel synthesis. By varying the relative concentrations of carbon dioxide and steam, the hydrogen to carbon monoxide product ratio can be controlled as required by the desired type of synthetic fuel being produced from the syngas. The resultant synthesis gas has been used as the feedstock to produce synthetic methane and Fischer Tropsch liquid fuels.Alkaline and proton exchange membrane electrolysis cells typically operate below 100°C, while solid oxide electrolysis cells operates in the 750-850°C range. This higher temperature improves the efficiency significantly. Practically, it translates into a lower cell operating voltage, 1.1-1.4V for high temperature electrolysis vs. ~1.8V for water electrolysis. Hydrogen production is stoichiometric with current in all types of electrolyzers.Carbon dioxide is a valuable resource as a feedstock for energy storage as a hydrocarbon. There is a vast amount of renewable energy that cannot be effectively utilized as grid electricity, but which could be used to convert CO2 to hydrocarbons, offering a solution to the even more difficult (than supplying grid power) challenge of production of sustainable, domestic transportation fuels. Conventional electrolysis and chemical processes could be deployed to accomplish this conversion. However, high temperature co-electrolysis of CO2 and steam to produce synthesis gas using solid oxide fuel cell technology has the potential of improving the efficiency by nearly 50%. A domestic synfuel industry will enable a much larger reliance on intermittent renewable energy than can be accommodated by conventional electric demand profiles while increasing our energy security."

Jan 1, 2010

By Yoshinao Kobayashi

he removal of oxygen from titanium and zirconium is important for use in application because it significantly affects the mechanical and physical properties such as ductility and toughness. However, thermodynamic properties of oxygen in molten titanium and zirconium have not been clarified and the effective deoxidation process of molten titanium and zirconium has not been established. In this study, the standard Gibbs energy of reaction of oxygen and yttrium in molten titanium and zirconium have been measured by a chemical equilibrium technique. Molten titanium, zirconium, and their alloys with aluminum were equilibrated with a Y2O3, A12O3, or Zr02 pellet in a cold crucible. The results are summarized as follows:

Jan 1, 2000

By Sheng-li Wu, Guo-liang Zhang, Bo Su

The mineralogical characteristics of iron ores can influence their high temperature sintering performance. In this study, eight iron ore samples from Brazil, Australia, and South Africa were characterized by their chemical composition, mineral types, particle morphology, and gangue dispersity. Meanwhile the influence rules between the mineralogical characteristics and the high temperature characteristics were evaluated and analyzed. The results showed that the effect of SiO2 on assimilation characteristic of iron ores was relatively complex, Al2O3 and LOI of iron ores had negative correlation with assimilation temperature of iron ores, the dense slab-flaky mineral granule restrained to the assimilation characteristics of iron ores; liquid phase of iron ores with high SiO2 content and low Al2O3 content had high fluidity, and the higher dispersity of gangue minerals in iron ores was good to the fluidity of liquid phase.

Jan 1, 2015