Search Documents

By William A. Apel

Several different strains of bacteria have been shown capable of reducing hexavalent chromium, Cr(VI), to Cr(III), a less toxic, .. more readily recoverable form of Cr. This paper examined the Cr(VI) reduction efficacies of 3 different Cr(VI) reducing bacteria: Pseudomonas f1uorescens LB300., Pseudomonas aeruginosa PAOI, and Pseudomonas aeruginosa PAOI (pCROI) It was demonstrated that all three bacterial stratns reduced Cr(VI) primarily during their exponential growth phases while using glucose as their carbon and energy source. Significant differences in the three organisms' Cr(Vl) reduction capabilities depending on initial Cr(VI) concentrations were also demonstrated. P. aeruginosa PAOI showed superior Cr(VI) reducing capabilities over the. entire range of Cr(VI) concentrations tested while the Cr(VI) reduction capabilities of the other two strains were increasingly inhibited as Cr(VI) concentrations increased.

Jan 1, 1991

By Yijia Dong, Mingjun Rao, Pengxu Cao, Jun Luo, Guanghui Li, Zhiwei Peng

Coal fly ash (CFA), as a by-product generated from coal fired power stations, is widely used for autoclaved concrete block production. It has been found that the generation of tobermorite is great benefit to the block strength during autoclaving. In this study, the tobermorite fibers synthesized from CFA and lime via the hydrothermal process are used as the revulsive to promote the mechanic strength of the concrete blocks. The results show that tobermorite fibers with 0.01–0.5 lm in diameter and 1–3 lm in length are obtained at 200 °C for 0.2 h. As the addition of prepared tobermorite fibers increases from 0 wt% to 2.0 wt%, the compression strength of concrete block increases from 24.6 to 40.5 MPa, and the compression strength of aerated concrete block produced under the optimized conditions can reach above 7.5 MPa.

Mar 1, 2018

By Richard J. Abitz

Thennodynamic geochemical models have been applied to assess the relative effectiveness of a variety of reagents added to aqueous waste streams for the removal of radioactive elements. Two aqueous waste streams were examined: effluent derived from the processing of uranium ore and irradiated uranium fuel rods. Simulations of the treatment train were performed to estimate the mass of reagents needed per kilogram of solution, identify pH regions corresponding to solubility minimums, and predict the identity and quantity of precipitated solids. Results generated by the simulations include figures that chart the chemical evolution of the waste stream as reagents are added and summary tables that list mass balances for all reagents and radioactive elements of concern. Model results were used to set initial reagent levels for the treatment trains, minimizing the number of bench-scale tests required to bring the treatment train up to full-scale operation. Additionally, presentation of modeling results at public meetings helps to establish good faith between the federal government, industry, concerned citizens, and media groups.

Jan 1, 1996

By S. C. Sharma

The aluminium matrix composites with ceramic dispersoids can be separated by density difference concept. In the proposed work composite scrap is recycled using an oil fired furnace. The scrap is melted in the furnace and temperature is maintained below 740 degree centigrade. Because of the density difference the lighter dispersoids will float and heavier dispersoids will settle down. The clean melt is separated be removing the floating and settled disperssoils, and then filtering using ceramic filters.

Jan 1, 1995

By Benoit DeBecker

Laboratory-scale experiments have shown that chromium metal could be recovered from chromate wastes by modifying slightly the chromium electrowinning flow-sheet. After reduction by sulhr dioxide and precipitation of chromic hydroxide, the solid residue is dissolved in the chrome alum solution and the metallic impurities are removed by cementation on manganese. The presence of dissolved manganese in the electrolyte does not affect the cathodic deposition of chromium and it eliminates the anodic production of Cr(V1).

Jan 1, 1994

By Nozomu Hasegawa

The phase diagrams and microstructures of the slags in the Mitsubishi Continuous Copper Smelting and Converting Process were studied for the prevention of the magnetite troubles such as accretion build-up on furnace hearths and launders, blockages at the melt outlet, slag viscosity increases and so on. According to the results of those studies, the silica and lime contents in the silicate slag at the smelting furnace, and the lime content in the lime-ferrite slag at the converting furnace were changed, resulting in lower and more consistent copper levels in the discard slag, with much less need for operators to clean melt outlets and launders. However, these changes may decrease the desirable amount of accretion-coating inside the furnaces and thereby reduce furnace campaign lives. Therefore, a method of estimating the magnetite level in the melts was developed, and slag compositions and temperatures have been controlled within the appropriate ranges to prolong furnace lives and also prevent magnetite troubles.

Jan 1, 2003

By J. P. Bellot

During the non-ferrous metal processing, the melting step under vacuum or under rarefied gas leads to volatile metal losses. It is the case of the metallurgical processing of the nickel-based, titanium-based or zirconium-based alloys where the evaporation losses don't allow a sufficient control of the alloy chemical composition. A theoretical approach has been carried out involving both a continuum description in the liquid phase and a molecular approach in the rarefied gas phase. The finite volume method is used in order to solve the coupled transport equationsin the liquid, whereas the Boltzmann equation is modelled by using a Monte Carlo method. At the liquid metal and metallic vapor interface, the volatilization and recondensation fluxes link up the two calculations. Simulation results are given for the melting and refining of reactive metals such as titanium alloys where the control of the chemical composition remains a major difficulty. The validity of the kinetic Langmuir's law is discussed for different operating conditions.

Jan 1, 1996

By Kazutoshi Haga, Atsushi Shibayama, Altansukh Batnasan

This study presents a viable approach for recovery of precious metals such as gold (Au), silver (Ag), palladium (Pd), and base metals, including copper (Cu), nickel (Ni), cobalt (Co), lead (Pb) and zinc (Zn) from waste printed circuit boards (WPCBs) via iodine-iodide leaching and precipitation. The behaviours of dissolution and precipitation of precious and base metals during iodine-iodide leaching and precipitation processes were discussed. Sodium hydroxide (NaOH) was used to remove base metal impurities exist in the pregnant leach solution under alkaline conditions. Precious metals remained in the resulting solution from NaOH precipitation were recovered by reduction using ascorbic acid (L-AA) solution. Results show that under optimum leaching conditions, almost all (> 99%) of Au was dissolved in an iodine-iodide solution when the dissolution efficiencies of other precious metals (Ag, Pd) and base metals, besides calcium (leaching of 25%) were less than 1 and 6%, respectively. The study revealed that more than 95% of Cu, Ni, Pb, Zn, Fe and Mn were initially removed from the pregnant leach solution at pH of 9.3 with addition of 0.1 M NaOH. Then 99.8% Au, 81.7% Ag and 74% Pd were precipitated from the obtained solution after NaOH precipitation while L-AA dose was 0.6 ml/ml at the condition. It can be concluded that the precious and base metals could be recovered selectively and economically from WPCBs via iodine-iodide leaching followed by precipitation using NaOH and L-AA.

Mar 1, 2018

By Isauro Rivera Landero, Martín Reyes Pérez, Eduardo Cerecedo Sáenz, Javier Flores Badillo, Mauricio Guerrero Rodríguez, Juan Hernández Ávila, Eleazar Salinas Rodríguez, María Isabel Reyes Valderrama

During column flotation of mining tailings of the Dos Carlos dam, it was observed that the effect of surface liquid flow (JL) is a variable that determines the rate of rise of packing bubbles and therefore, causes the generation of gas retained within the columnar system. Also overall more stable laminar flows were observed, in a range of superficial flow of liquid in the bottoms stream (JLT) from 0.446 to 0.68 cm/s, showing the stability in the range of superficial gas flow (Jg) from 0.1 to 0.5 cm/s. Observing a uniform bubble size for the three JLT evaluated, with a diameter between 0.05475 and 0.2525 cm, at all the range evaluated of Jg. Furthermore, an uniform performance was obtained, and with the same rate of rise of packing bubbles, showing a greater packing bubbles at JLT = 0.446 cm/s, due to the lesser bubble size observed, in comparison with the values of JLT of 0.68 and 1.017 cm/s.

Mar 1, 2017

By Baohua Li, Yanhui Liu, Shengping Li, Xuewei Lv, Yun Chen

There are almost ten billion tons of vanadium-bearing titanomagnetite in Panzhihua-Xichang area. However, iron ores in Hongge, which has the most abundant reserves in the four mine areas in Panzhihua, have not been utilized sufficiently so far. The reason behind this is the relatively high Cr2O3 in the ores (0.49 %~0.82 %), that due to its high melting temperature will negatively influence the blast furnace reduction and slagging process. Therefore, in the blast furnace process, Cr is hope to be reduced into molten iron, which can reduce slag viscosity problems. Slag iron reduction experiments were conducted to quantify the Cr reduction. Experimental results shows that with the increase of TiO2, the content of Cr in the hot metal is decreased when balanced. And during the initial stage of the reduction reaction, the reaction kinetic model is a first-order reaction.

Jan 1, 2016

By Xiaoming Huaa

The effect of the anodic polarization on the composition and morphology of the surface layer formed on chalcopyrite during ammonia–ammonium chloride leaching was investigated. The anodic polarization on the chalcopyrite electrode was used for oxidation and dissolution of chalcopyrite, and the resulting oxidized layers were characterized by XPS, SEM and optical microscopy. The results show that oxide layers exist on the chalcopyrite surface with or without any anodic polarization in the leaching solution at ambient atmosphere. However, the composition and morphology of the layers are strongly depended on the extent of polarization. The distribution of FeOOH and Fe2O3 within the oxidized layer was inhomogeneous for the sample at the open circuit potential (OCP). The composition and morphology of the oxidized layers which were formed at anodic potentials lower than 0.3 V versus SCE were similar to those of the chalcopyrite at the OCP. At anodic potentials above 0.4 V, the oxidized layers contained many cracks, and they were fragile and exfoliated. Furthermore, the sulfide had been oxidized to sulfur species with higher oxidation states. The oxidation of the chalcopyrite seemed to undergo a cyclically oxidative process that suggested growth and spallation of oxidation layers on chalcopyrite in a layer-by-layer sequence.

By A. Treverrow, G. A. Brooks, H. K. Worner

"The work by H.K Worner and co-workers at CRA in the 1960s, and early 1970s, established that molten metals could be refined continuously utilising counter current flow of metal and slag. Womer also demonstrated that counter current refining could produce highly refined metal products. These developments coincided with the advent of high intensity metallurgical reactors in both the ferrous and non-ferrous industries (e.g. BOS, Q-BOP and later Sirosmelt) that utilised high levels of gas injection to produce rapid stirring and very fast reaction. These new generation of high intensity metallurgical reactors allowed high tonnage rates through relatively small volume vessels.Whilst, it is well known that the counter current flow of reacting phases offers the potential of efficient mass transfer and high purity products, the application of counter current reactors to molten metal/slag systems has been criticized on the basis that they suffer from either low intensity or, alternately, from poor refining due to excessive dispersion. These criticisms relate to the balance between intensity and the refining capacity of a reactor. That is, whilst high levels of mixing transversely to the direction of flow promotes high mass transfer, longitudinal mixing (dispersion) is detrimental to refining. Of course, mixing in one direction invariably leads to mixing in other directions, thus creating a playoff between high mass transfer and excessive dispersion.This balance between intensity and refining has been the subject of recent studies overseas, and at"" the University of Wollongong, using cold modelling techniques to evaluate the effect of mixing on dispersion in a counter current refining launder. These studies have shown that for a given geometry and mixing regime, dispersion decreases with increasing flow of liquid phases. This means that whilst high mass transfer cannot be achieved in a refining launder without sacrificing the degree of refinement, there is no impediment to achieving high productivity through such a system, in fact, high through puts may favour good refining. Thus, it may be possible to match a high productivity smelting operation with a equally productive counter current refining stage."

Jan 1, 1996

By Esperidiana A. B. Moura, Célio H. Wataya, Roberta A. Lima, Rene R. Oliveira

The purpose of this study was to investigate the mechanical, morphological and thermal properties of biodegradable composites based on aliphatic-aromatic copolyester/polylatic acid blends (PBAT/PLA blends) reinforced by açaí seed fibers, an abundant byproduct of the açaí fruit agro industry. The biodegradable polymeric composites were prepared by melting extrusion process using a twin-screw extruder machine. The fibers removed from the açaí seed were used as the reinforcement and PBAT/PLA blends as the matrix. The influence of the açaí seed fibers addition on properties of composites was investigated by tensile and impact tests, SEM, DSC, and XRD analysis. Correlation between properties was discussed. In addition, açaí seed fibers characterization by SEM, XRD and WDXRF have also been carried out. The addition of açaí seed fibers on biodegradable PBAT/PLA blends showed that it is possible to get interesting property gains in biodegradable polymer by using waste from renewable sources.

Jan 1, 2015

By Baozhong Ma, Chengyan Wang, Yongqiang Chen, Peng Xing

This paper introduces an oxygen-enriched flash smelting (OFS) process for lead smelting. Compared with the bath smelting, OFS has many advantages, including wide adaptability, high yield, low energy consumption, little uncontrolled emission, and considerable metals recoveries. Test results showed that increasing CaO could effectively reduce lead content in the slag, and the appropriate mass ratios of FeO-to-SiO2 and CaO-to-SiO2 were 1.15 and 0.6, respectively. The testing and commissioning indicated when OFS was used to treat material containing 30% of lead, the residual lead in slag could decrease to 4–10%. Furthermore, after zinc volatilization using an ore-smelting electric furnace, contents of lead, zinc, silver, gold and copper in the final slag were below 2%, 2%, 6 g/L, 0.1 g/L and 1%, respectively. The total recoveries of lead, zinc, silver, gold, copper and sulfur were above 98, 90, 99.5, 99.5, 85 and 98%, respectively.

Mar 1, 2018

By Long Meng, Yaodong Yi, Kuiyuan Chen, Zhancheng Guo, Yu Li

Blast furnace slag is the main by-product discharged in the iron and steel industry and contains considerable waste heat at dischargeing temperature between 1450 and 1550 °C. To fully utilize waste heat and slag, this study directly converted high temperature liquid Ti-bearing blast furnace slag into glass-ceramics via the “Petrurgic” method. Samples at different crystallization temperature were prepared and its influence on crystal phases, pore structure, and compressive strength were investigated via SEM, XRD techniques, and compressive strength measurements. Results showed that all glass-ceramic samples contained main crystals of perovskite, diopside and gehlenite and had a qualified mechanical performance with compressive strength above 100 Mpa, which meets the requirement of Chinese national standard for natural granite stone. With increasing crystallization temperature, pore size decreased, while the size of the perovskite phase firstly decreased and then increased with decreasing crystallization temperature. Samples had an optimum crystallization temperature of 1215 °C, maximum grain size and a densified structure with minimal pore defect.

Mar 1, 2018

By M. I. Hoschke

The viability of pyrometallurgically treating zinc containing materials is enhanced by recovering zinc metal rather than oxide from furnace gases. During the history of zinc production, there has been continuing development on methods of recovering zinc metal that has resulted in three commercial designs in use today. The most widely used commercial technology, currently producing 13% of the world's zinc, is the lead splash condenser which is attached to the Imperial Smelting Furnace (ISF). The other remaining commercial designs are the zinc splash condenser and the Wheaton-Najarian vacuum condenser. The need to treat increasing quantities of secondary zinc materials, particularly Electric Arc Furnace (EAF) dust, has renewed emphasis on the development of ways to recover zinc metal. Development work in this area has proved to be difficult. Partly as a response to these difficulties, studies into the fundamentals of zinc condensation and absorption have been undertaken. Pasminco Research Centre (PRC), Newcastle, is also developing a. new zinc absorber to recover zinc metal from furnace gases:. The design attempts to address the problems associated with current devices.

Jan 1, 1994

By Jingwei Lou, Bing Li, Suzhen Li, Miao Shen, Jianguo Yu

"As a main impurity in primary lithium metal, magnesium is difficult to remove because of the very close relative volatility of the two metals. Electrochemical refining provides a possibility to completely remove Mg in the LiCl-KCl melt prior to Li reduction. MgCl2 reduction processes in LiCl-KCl- MgCl2 melt were investigated by cyclic voltammetry (CV), square wave voltammetry (SWV), chronoamperometry and chronopotentiometry. Then potentiostatic electrolysis was carried out and Mg (II) ion was reduced onto a liquid lead cathode from the LiCl-KCl-MgCl2 melt at the Mg deposition potential. The results show that Mg ( II ) is reduced in one step with two-electron transfer. The reduction potential of Mg ( II ) was well defined. The reduction of Mg( II) results in Li ( I ) underpotential deposition at 0.2V more negative potential than that of Mg( II) reduction. Therefore, in order to prevent Li ( I ) from codeposition with Mg, accurately controlling Mg ( II) reduction potential during the potentiostatic electrolysis was necessary. Ninety three to 99 % removal rate of MgCl2 was achieved after 8-12 h electrolysis when liquid lead was used as cathode.IntroductionMetallic Li has been widely used in batteries, light weight alloys and in fusion reactors because of its excellent properties. Currently, the only way in industry to produce metallic Li is by electrowinning from molten LiCl-KCl at about 450 °C [l-5]. LiCl-KCl is the only electrolyte used, because they presents a lower eutectic temperature and KCl shows a slightly higher theoretical decomposition voltage than LiCl, as shown in Table l .The produced metallic Li generally contains 1-2 wt% impurities including Na, K, Al, Ca, Mg, Si, etc. [6l, which are derived from the corresponding metal chloride compounds or metal oxide compounds existing in the LiCl and/or KCl raw materials. These impurities have to be removed by subsequent vacuum distillation at high temperatures to meet the requirements for metal Li purity in the final products. Separation of Mg from Li by vacuum distillation is difficult because their relative volatilities are very close, as shown in Table 2."

Jan 1, 2011

By E. Fregeau-Wu

The major obstacle in recycling steelmaking slags to the blast furnace is their phosphorus content. Removal of the phosphorus, which is primarily associated with the silicate and phosphate phases, would allow for greater recycle of these slags for their iron, manganese, and lime contents. Calculations show that separation of the silicates from the oxide phases would remove nearly 90% of the phosphorus from the slag. The variable grain size of the as-received slag made liberation by fine grinding difficult. Therefore, slow-cooling experiments were undertaken to improve the grain size distribution. The grain size distributions were determined using in-situ image analysis. The samples were ground to their apparent liberation size and high gradient magnetic separation was used to separate the magnetic oxides from the nonmagnetic silicates and phosphates. Liberation analysis and modeling was performed on selected separation products for discussion of benefication characteristics.

Jan 1, 1995

By Na Wang, Chao Du, Hongmin Zhu, Kai Huang, Shuqiang Jiao

"Niobium aluminides were directly synthesized by a sodiothermic reduction process of NbC15 - AlCb which was dispersed into LiCl - KCl - NaCl - CaCb melts. The melt supplied a homogenous reaction medium which was substantially beneficial to the co-reduction of Nb and Al to form niobium aluminides in situ. The reduction was performed at 500°C for 4 hours. The products were analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM). The corresponding results indicated that niobium aluminides powders were successfully synthesized.1. IntroductionNiobium aluminides have received considerable attention as high-temperature structural materials, due to their high melting points, relatively low density, high strength, excellent oxidation and creep resistance [1-4]. Figure 1 shows that there are three intermetallic compounds in the Nb - Al binary [5], which includes Nb3Al (A15 structure, Cr3Si type), Nb2Al (D8b structure, cr-CrFe type) and NbAb (D022 structure, TiAb type). These niobium aluminides have been used in turbine blades or in stationary gas turbines [6-8]. However, despite their attractive features, the ir applications are still limited by the long and costly fabrication process [9, 10].Niobium aluminides were industrially fabricated by the mechanically alloyed process [11-13]. Traditionally, niobium is extracted from Nb2O 5 or K2NbF7 by a metallothermic reduction process while aluminum is produced by the Hall-Heroult process of Ah03 electrolysis. Based on the extraction of Nb and Al, respectively, niobium aluminides is synthesized by a mechanical powder alloying process. The present process for making niobium aluminides requires a set of complicated equipment, has high production cost and time consuming [14, 15].The purpose of this work is to present the simple, economic and direct synthesis of niobium aluminides powders utilizing a sodiothermic reduction from NbC15 - Al Cb dispersed into molten salts."

Jan 1, 2011

By J. L. Sanchez

Using a special double-zone transpiration reactor, the vapor transport chemistry of vanadium pentoxide in the presence of water vapor has been investigated. Three possible volatile hydroxides above V,O,(s) are reported in the literature: VO,(OH),, V,O,(OH),, and VO(OH),. In the present study, it was established that VO(OH), is the principal gaseous hydroxide species formed. The predominant reaction was found to be: { } The vapor pressure of VO(OH), was measured as a function of temperature, water pressure, oxygen pressure and flowrate. The results have been used to determine the Gibbs free energy of the above reaction as a function of temperature: { } The results of the present work were combined with thermodynamic data reported in the literature to obtain expressions for the AGO for the reaction above V,0,(1) and the AGO of formation (units in cal/g-mole).

Jan 1, 1993