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By Patrick R. Taylor

This investigation studied the inflight calcination kinetics of nuclear waste simulant using a thermal plasma reactor. A series of experiments were performed to determine the conversion of insoluble aluminum compounds to the soluble compounds and the decomposition of complex organic and nitrite compounds present in the simulant waste. Thermodynamic calculations based on free energy minimization were performed to establish a theoretical basis for this investigation. A kinetic model to describe the conversion of gibsite to sodium aluminate has been proposed. The products of the calcination were characterized using XRD, Gas Chromatography, and chemical analysis by ICP. The results of this investigation indicated 85% gibsite conversion to sodium aluminate, 90% of nitrate decomposition, 52% TOC decomposition and 90% conversion of chromium to soluble compounds. A process is identified for inflight calcination of wastes. Key words: Plasma, waste, simulant, calcination

Jan 1, 1996

By Harrison Hodge

In the Bayer process for alumina production, between 2–35% Al2O3 is lost with bauxite residue due primarily to incomplete dissolution of aluminiumbearing minerals during caustic leaching or the precipitation of sodium alumino-silicate solids. The recovery of sodium and aluminium from the residue, and particularly from the contained sodium alumino-silicates, is becoming an increasingly critical issue from both an environmental and economic standpoint. Lime-soda residue sintering followed by selective leaching has been proposed as a method to recover sodium and alumina. The factors influencing the sintering mechanisms and kinetics, and the subsequent leaching have not been well described to date. In this study, the physical and chemical changes taking place during isothermal sintering of bauxite residue in air, particularly at short reaction times are investigated using scanning electron microscope (SEM) and X-ray diffraction (XRD). The impacts of these changes on the recovery of valuable materials are reported.

By Kandipati Sreenivasarao

A promising method for removing heavy metal ions from dilute effluents is ion- or precipitate- flotation, in which a suitable collector is added to form hydrophobic metal-collector complexes or compounds that can be collected as foams. We have successfully removed Cu(II), Cd(II), and Pb(ll) from dilute solutions using sodium dodecylsulfate and ethanol as collector and frother respectively. However the process would not be economically viable unless the collector could be recycled, and the heavy metals recovered in a concentrated, preferably marketable, form from the foams. We investigated four different methods to decompose heavy metal-dodecylsulfate complexes, namely precipitation of hydroxides, precipitation of sulfides, chemical stripping, and electrolysis. We compare the performance of these methods. In each case the observed behavior is related to known thermodynamic data, and potential applications are discussed.

Jan 1, 1995

By Jian Ye

Recycling of aluminum scrap, such as Used Beverage Container (UBC) scrap is steadily increasing. In secondary remelting of such scrap, it is a common practice to use protective molten salt cover. An appropriate salt protects metal from oxidation, promotes coalescence of the suspended metal droplets, and separates clean metal from the oxide contamination. The molten salt also reacts with metal. This causes metal loss and change of resulting metal composition. In this paper, role of molten salt fluxes in melting of UBC scrap is discussed, and selection criteria for molten salt are provided.

Jan 1, 1995

By C. T. Philipp

Recycling of waste is much preferred over disposal. This paper discusses the Enviroscience, Inc. (ESI) process, now being commercialized by MetWool, Inc., to recycle hazardous wastes using an extractive metallurgical process which is followed by vitrification of non-reducible metal oxides. In this process, volatile and reducible metals are reclaimed as their respective oxides and elements.

Jan 1, 1995

By Olga Slavkina

A new technology of bacterial leaching by means of the Thiobacillus ferrooxidance bacteria is proposed. The equations of reactions that describe of the first and the second stage of bacterial leaching of sulfide raw materials containing non-ferrous metals are given. The theory is analyzed and the technology of processing of some complicated substandard concentrate containing copper and zinc is proposed. The main technological operations including a two-stage bacterial leaching and stages of copper and zinc recovery in the form of marketable product are described. The results of the experimental validation of the main technological parameters of the first stage are given. The main possibilities of a more complete zinc and copper recovery at the second stage of bacterial leaching are discussed in comparison with single-stage leaching process.

Jan 1, 2003

By Francois Reizine

Infrared sensors will include scanning detectors and positioning sensors. The focus will be on 1, 2, and 4-color wavelength pyrometer systems which allow the accurate measurement of emissivity and, consequently, of the true temperature even in the presence of scale, slag, and fumes. Such sensors are being used in blast furnaces, BOF's, and galvanizing lines. Laser sensors will be presented using different principles of physics, mainly time-of-flight, pulsed infrared lasers for level measurement and dimensional measurement; triangulation lasers for width and thickness measurements; and laser Doppler velocimeters for velocity and length measurements, including mass flow, elongation, and tension control, cut-to-length applications. These sensors and systems are based on state-of-the-art technical developments to improve productivity and quality and reduce maintenance and downtime.

Jan 1, 2001

By D. Q. Cang, G. Duan, H. X. Li, H. Bai

"Life cycle assessment (LCA) is a valid environmental evaluation method and enterprise environmental management tool used in industrial ecology areas. In this paper LCA was newly used to evaluate the environmental impact of manufacturing of alumina by Bayer process in china from two aspects of logistics and energy flow, GaBi software acted as analysis tools with evaluation model established, and several environmental impact assessment criteria were selected based on the actually typical date of Bayer alumina producing process. Evaluation results show that alumina manufacturing by the Bayer process has a great impact on the global warming and human health of respiration, even roasting process gives rise to the greatest impact of winter fog index. Scenario analysis proposed ways of reducing environmental load caused by Bayer process including: (1) the economic and efficient use of mineral processing technology; (2) optimization of energy use, saving power consumption or the use of new more economical source of energy; (3) actively promote the use of innovated technology and equipment in alumina manufacturing and waste such as red mud utilization process.1 IntroductionSince 2002, China is already the world's biggest producer of aluminium, in 2007, China aluminum production has accounted for above 1/3 all over the world, 2009 for 13 million tons and to the end of 2010, China aluminum production is expected increased to be over 15 million ton [1,2,3]. While as the raw material for producing aluminum the alumina production in china has up to 19.46 million tons of the world's total quarter in 2007, by the end of 2009 China alumina production has achieve to 23.78 million tons [4,5]. China has rich bauxite resources with proven reserves about 23 million tons, but the great majority of china bauxite is hard monohydrate diaspore type with low ratio of aluminium silicon, high impurity content and poor aluminum dissolution performance, that cause high energy consumption, long and complex process, high production costs and heavy environment load[6,7]. Before most used alumina production was sintering process rather than Bayer method in china, over the past decade Bayer method has been widely applied instead of sintering process or combination both forming joint process, premise is improving bauxite quality by mineral processing or adding imported rich bauxite mineral[6,8]. In general each ton production of alumina needs bauxite 1.6~2.20t, limestone 0.7~1.7t, soda 0.250kg, fresh water 12.30 cubic meters, in addition to consume large amounts of energy, and emission waste water over 8.0 cubic meters, dust 2.3~5.7 kg, red mud 0.8-1.5 tons. In china Red mud yield nearly 30.0 million tons every year, accumulated stock is approximately 0.2 billion tons, by 2015 accumulative total red mud is expected to reach 0.35 billion tons [9-13].We know aluminium industry and alumina production have produced large waste, make large energy consumption and its environmental impact could not be ignored. Expecting to optimize production processes and achieve resource recycling for this industrial process the proper environmental assessment is very necessary. Currently Life Cycle Assessment (LCA) is generally recognized as the approved tool to achieve the purpose. The essence of LCA tool is to examine, identify and evaluate a kind of materials, product, process, or a system of environmental impact in their whole life cycle. The life cycle of materials or products includes whole process from raw materials obtained to the final disposal, or more ideal with original or other forms of the whole process of recycling [14-17]."

Jan 1, 2011

By Tae-Hyun Kim, Kang-In Rhee, Jeong-Soo Sohn

The synthesis of Mn-Zn ferrite powder from spent zinc-carbon batteries was investigated using a series of physical treatment, sulfuric acid leaching and coprecipitation. Physical separation methods such as crushing, magnetic separation and sieving were applied to generate a non-magnetic material of 8- mesh undersize for subsequent leaching process. The 8-mesh undersize of the spent zinc-carbon batteries was assayed 23.9% Mn, 14.9% Zn, and 4% Fe. Metal extractions obtained in sulfuric acid leaching at the solid/liquid ratio of 1:10, 2 M H2SO4, and 60? with 6 vol.% H2O2 addition were 97.9% Mn, 98.0% Zn and 55.2% Fe. The leach liquor was finally adjusted to the Mn:Zn:Fe mole ratio of 1:1:4 suitable for producing MnZnFe4O8 ferrite powder by the addition of Mn, Zn and Fe sulfates followed by pH control. A co-precipitation test for Mn-Zn ferrite powder was performed at 80?, O2 gas flowing at 1.3 L/min. As a result of co-precipitation, Mn-Zn ferrite nanoparticles in 20 nm size with spinel structure were successfully synthesized. The saturation magnetizations of Mn-Zn ferrite powder (Mn1-xZnxFe2O4) were determined to be 39-91 emu/g with various zinc contents (X=0.2-0.8).

Jan 1, 2008

By G. H. Khoe

Although some hydrometallurgical process liquors contain significant amounts of ferrous and arsenate ions, no reliable thermochemical data for the aqueous complexes and the solubility of the ferrous arsenate precipitate are available. The complexation of iron(11) with arsenate has been investigated using the potentiomemc titration method. The results indicated that virtually no complexation of iron(@ with arsenate has been observed. This is in contrast to the significant complexing reported for iron(1n) with arsenate. The solubility product of the precipitate was calculated using the concentrations of appropriate arsenate species pertaining to the observed precipitation pH's. The fit of the observed precipitation points on the solubility curve of the computed stability diagram was used to assess the appropriateness of the equilibrium model.

Jan 1, 1991

By Xiang Ma, Halvor Dalaker, Kai Tang, Stefan Andersson

Silicon carbide (SiC) is one of the most important non-oxide ceramic materials for many industrial applications and is mainly synthesized by carbothermic reduction of silicon oxide by coke above 2200°C. Replacing natural gas (mostly methane, CH4) for coke in SiC synthesis could considerably reduce energy consumption and CO2-emissions owing to higher carbon activity of CH4 at lower temperature. The generally accepted reaction mechanism is that SiC is synthesized through gaseous intermediate silicon monoxide, SiO. In the present study, the reaction mechanism for the SiO and CH4 gaseous mixture has been examined using atomic scale modelling. Molecular dynamics (MD) using a reactive force field (ReaxFF) has been utilized to examine the initial stages of reactions involving a gas mixture of SiO and CH4 and surfaces of SiC. The MD results revealed some interesting SiC formation mechanisms. The reaction energies of the critical intermediate species were also estimated by density functional theory (DFT) calculations and the implications for the force field parameters used in ReaxFF was discussed.

Jan 1, 2015

By Yotamu Stephen Rainford Hara, Animesh Jha

The investigation focuses on a low temperature recovery of Cu and Co from a 40 wt% SiO2-(30 wt%Fe,6 wt%Al)2O3-10wt% CaO-7wt%CuO-7wt%CoO slag over a temperature range of 1173K to 1323K. The alloy phases containing Cu-Co and Fe-Co alloy formed via the carbothermic reduction of oxides: MO + C = M + CO(g), where M represents metallic copper, cobalt or iron. In the direct reduction of oxides, the recovery of metallic phase was well below 90% at 1323K, due to the kinetic barrier which was analysed and attributed to oxygen and metal-ion transport in the slag. This barrier was overcome by adding CaSO4 and carbon, which yields a matte (MS) phase via MO + CaSO4 + 4C = MS + CaO + 4CO reaction. Lime thus produced in situ participates in metal oxide/metal sulphide reduction reactions, which are analysed with the help of X-ray powder diffraction, scanning electron microscopy, and thermogravimetric analysis.

Jan 1, 2014

"Hematite pellets were electro-deoxidized to iron in molten sodium hydroxide to produce iron containing about 10-wt % oxygen. The anodic reaction was the evolution of oxygen on an inert nickel anode. Before the electrochemical reaction, there is a reaction between sodium hydroxide and ferric oxide to form sodium ferrite and, in order to compensate for the reduction in sodium oxide content, 1 wt % sodium oxide is added to the melt. In a laboratory cell, the cell voltage was 1.7 V with a current density of 5000 A m-2, a current efficiency of 90% and an energy consumption of 2.8 kWh kg-1.Introduction The iron and steel industry contributes about 2.3 bn tonnes/annum of the carbon dioxide to the atmosphere, which is about 10% of the total, and some believe that, in order to prevent a catastrophic rise in the earth’s temperature, carbon dioxide emissions must be reduced by 50% come 2050. However, by 2050, it is likely that the iron and steel industry would have grown significantly so that the production may have risen to 2 or 3 bn tonnes/year so in order to meet the 50 % reduction on today’s figure, the carbon dioxide may have to be reduced to 25% or less, which is a very demanding requirement. There are probably three ways of reducing the carbon dioxide output:1. By capture and sequestration, but this may be technically very demanding.2. Reduction using hydrogen in place of carbon."

Jan 1, 2009

By Jennifer Mager, G. P. Martins, Dean Mussatti

"The role of lead, at low concentrations in high pH cyanide-electrolytes, on the dissolution behavior of gold, has been a topic of scientific and industrial concern for well over a century. The recent paper by Kondos et al [1] at CANMET (1995) this continuing interest and apparent importance. Nevertheless, the mechanism(s) by which this (and other heavy metal) component influences the electrodics of this electrochemical system has still not been unequivocally demonstrated. Instead, several plausible hypotheses, by pioneering researchers in this field, have been advanced and reiterated OVer the ensuing years. While it is generally accepted, based on equilibrium elctrode-potential calculations, that reduction (or co-reduction when oxygen is present in the electrolyte) of lead on the gold surface may occur due to cementation (contact reduction), the cemented lead has never been characterized. The work presented has reexamined the role of lead in this system, by delineating the species distribution of these system components and by interpreting the results of potentiodynamic studies in conjunction with SEM analyses of a gold electrode.1. INTRODUCTIONThe leaching of gold ores in cyanide electrolytes has been practiced for well over a 100 years. Research conducted on this topic has been primarily focused on the effects of operating parameters such as concentrations of oxygen and cyanide, and the pH of the electrolyte; or the leaching behavior of carbonaceous and sulfitic gold-bearing materials.Mechanisms by which pure gold is leached in alkaline cyanide media, with oxygen serving as the oxidant, have been subjected to continual examination and re-examination in the published technical literature during this century. Recently, it has been speculated that without the presence in the electrolyte of trace heavy metals, such as lead or mercury, that gold would not be leachable. Researchers who have tackled this topic, have either considered heavy metals to be a natural occurrence in these systems and ignored the role they may serve in the leaching process, or they have deliberately focussed on controlling their concentrations in the system to undetectable limits. As a result, conflicting findings have been reported for what would appear - depending on the details provided in these reports - to be identical systems."

Jan 1, 1997

By Jewel Gomes

Green rust is an important intermediate in oxidative transformation of Fe(II) phase. This unstable compound contains a mixture of ferrous and ferric hydroxides that belong to a family of minerals known as layered double hydroxides (LDH). Its general formula is [FeII(6-x) FeIIIx (OH)12]x+[Ax/n-*yH2O] x-, where A is an n-valent anion mainly Cl-, CO3-2 and SO4-2, and in which either the bivalent or the trivalent iron can be replaced for other trivalent or bivalent metal ions. It was first identified as corrosion product, later in soils as a product of interactions between microbes and metals in soils. Due to its high reactivity, it is used in the reduction of organic and inorganic compounds, As removal, and the treatment of acid mine drainage. In this paper, we described the method of electrochemical generation of green rust, its characterization by XRD, SEM and FT-IR, and its implications to electrocoagulation.

Jan 1, 2009

By René Winand

The paper gives a synthesis of research work performed in the department during the last ten years and dealing with cobalt , copper and manganese electrodeposition in chloride aqueous solutions. Special emphasis is given to electrocrystallization. For copper, properties of the electrolyte such as solubility limits, electrical conductivity and complex ions stability are discussed in connection with leaching, purification of the electrolyte, and metal recovery. When possible, kinetic parameters and probable electrode mechanisms are given. Problems that are still to be solved are also listed.

Jan 1, 1985

By C. G. Anderson

Throughout the world, there are many orebodies or materials which have significant value but also contain arsenic. As regulations on the transport, exposure, disposition and emission of arsenic have become more stringent; it has become increasingly more difficult to derive the values from these resources. This paper will outline the fundamentals of alkaline sulfide hydrometallurgy and its successful application to arsenic bearing ores, concentrates and materials.

Jan 1, 2005

By José Sancho, Julia Ayala, Purificación García, Begoña Fernández

"Electrofilter dust, a residue generated in the last stage of the Bayer process in the hydroxide aluminum calcination, was characterized to evaluate the alumina that was potentially extractable with sulfuric acid. The process studied aims to produce aluminum sulfate for water coagulant uses, taking advantage of the residues that accumulate in large quantities in the proximity of plants with difficult recycling for storage. Acid leaching is carried out at different concentrations of sulfuric acid, at different temperatures, pulp densities, and times, to dissolve gibbsite and transition aluminas. The result is an aluminum sulfate solution without iron and with commercial specifications.IntroductionElectrofilter dust is a residue generated in the last stage of the Bayer Process [1] in the hydroxide aluminium calcination. The residue is a mixture of alumina and hydrates which have not completed their calcination process.Electrofilter dust, composed by alpha alumina, gibbsite and transition aluminas [2] can be leached in an acid medium by putting most of the aluminium in solution; the remaining residue should be mainly andisolved alpha alumina. In many hydrometallurgical processes, sulphuric acid has been selected as the cheapest and the most effective leachant [3,4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15]The aim of this study is to determine the effect of temperature, acid concentration and pulp density on the sulphuric acid leaching of electrofilter fines for aluminium dissolution, in order to produce aluminium sulphate for water coagulant uses. This will provide a commercial product and at the same time eliminate the environmental problem created as a result of the storage of large quantities of electrofilter fines in the vicinity of the Bayer plant."

Jan 1, 2008

By C. A. Pickles

At the present time, pyrometallurgical processes are employed for the recovery of lead from battery scrap. These processes have serious pollution problems, primarily due to the emfssion of sulphur dioxide and airborne lead in the form of dust and fume. In addition it is necessary to dispose of solid wastes and liquid effluents which contain lead and in some cases sodium sulfide-containing compounds. In this work an improved process was investigated for the recovery of lead from battery residue. This involved pelletization of the residue with sodium carbonate and moisture. Then, the pellets were melted without carbon and the .sodium sulphate salt was removed. Subsequently, the molten lead oxide was reduced with carbon. This process minimizes the sulphur dioxide emissions and leads to very low sulfide contents of the sodium sulfate salt

Jan 1, 1992

By Jennifer Murphy, Brad S. Schake, Karol Holmes, John R. FitzPatrick, Mike H. West

"The separation and purification of uranium from either nitric acid or hydrochloric acid media can be accomplished by using either solvent extraction or ion-exchange. Over the past two years at Los Alamos, emerging programs are focused on recapturing the expertise required to do limited, small-quantity processing of enriched uranium. During this period of time, we have been investigating ion-exchange as a method for extraction/purification of uranium from acidic media. In addition, waste stream polishing is associated with this effort in order to achieve more complete removal of the uranium prior to recycle of the acid. Extraction chromatography has been demonstrated to further polish the uranium from both nitric and hydrochloric acid media thus allowing for a more complete recovery of the actinide material and creation of less waste during the processing steps.We will discuss contact experiments for evaluation of eleven different resins for uranium removal from nitric acid, the evaluation (again by contact experiments) of uranium elution from the ion-exchange media by various chemicals, and small-scale experiments for the removal of 235U from nitric acid. Larger-scale (1 DO-gram) flow experiments, using depleted uranium, were done after the small-scale evaluation of the selected resin. A discussion is also included concerning the shortcomings of the contact experiments and how the flow experiments were modified in order to overcome these problems. We will also discuss the application of ion-exchange for some specific process needs at Los Alamos.Contact experiments were used to evaluate some commercially available solvent-impregnated resins in addition to evaluation of several resins of this type synthesized in our laboratory. These experiments involved both nitric and hydrochloric acid media. The data from these experiments will be used to determine the column size and amount of resin required to polish the waste stream produced by the ion-exchange process described above. Small-scale flow experiments will be described and data given on the mass balances achieved using this two step process.Future work for evaluation of new ion-exchange and solvent-impregnated resins as well as the search for new eluants will be discussed. Other future experiments for both processes, including large-scale experiments, will be discussed in detail."

Jan 1, 1996