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By Laila A. Guirguis

Impurities are removed from crude phosphoric acid (57.75% P2O5) with a mixture of low and high molecular weight alcohols, one of which is hydrophilic and the other is hydrophobic i.e. methanol and hexanol. In a single stage, the phosphate values segregate to the high molecular weight alcohol fraction and the impurities segregate to the low molecular weight alcohol fraction. The optimum ratio for the extraction is found to be 0.5 part methanol, one part impure acid and four parts hexanol where an extraction percent of more than 95% is achieved. Re-extraction of the phosphate value from the solvent is obtained by 6% phosphoric acid and the different factors affecting the re-extraction process have been studied. Finally, the purified acid is concentrated under reduced pressure and passed through activated carbon column, whereas the alcohols are re-circulated. The produced phosphoric acid was found to be in good match with the international specifications of food grade quality acid. A technological flow sheet is elucidated.

Jan 1, 2006

By Hongmin Zhu, Guihua Wang, Xiangsheng Wang

"The anode process of carbon electrode in fluoride melt was studied by voltammetry and chronoamperometry. Anode gases were analyzed by gas chromatography on-line during controlled-potential electrolysis. Two peaks were observed on the cyclic voltammograms. According to the results of gas chromatography, the first peak was corresponded to the discharge of residual oxide ions, with the formation of CO and CO2. Discharge of fluoride ions occurred at 4.1 V vs. Li+/Li, and leading to the anode effect. With the occurrence of anode effect, small amount of CF4 was detected. As the potential reached 4.5 V, CF4 and C2F6 gas evolution occurred, and the current increased to form the second peak.1.IntroductionIn the primary production of Aluminum and some rare earth metals like neodymium, a departure from normal cell operation known as anode effect results in the generation of perfluorocarbons (PFCs), which have high global warming potentials [1]. Owing to the pressure of environmental protection, considerable research has been carried out to clarify the mechanism of anode effect and PFC generation of industry and laboratory cells in the aluminum electrolysis system [2-9]. The common result on PFC generation is that the PFCs are emitted from Hall-Heroult cells only when they are on anode effect. In this article, we selected LiF, the main electrolyte for the neodymium electrolysis [10-11], to perform further investigation on the underlying kinetics of PFC generation and the nature of the reactions at the electrode.2. ExperimentalAll experiments were carried out in an alumina tube reactor, which was filled with high purity helium atmosphere. Spectrographic graphite crucibles were used, which played the dual role of molten fluoride container and the counter electrode. Lithium fluoride was analytical grade. The experiments were carried out at 900 °C."

Jan 1, 2011

By Xiaorong Liu

Interfacial emulsion generated in copper solvent extraction is an inhomogeneous O/W emulsion that consists of organic phase, aqueous phase and solid particles. In order to determine what kind of components in organic phase promotes the emulsion, the organic phase separated from the interfacial crud provided by Dexing Copper Mine in Jiangxi, China was analyzed for its components by combined gas chromatography-mass spectroscopy. It was found that many kinds of emphiphiles containing such hydrophilic groups as carbonyl, carboxyl, or acylamine existed in organic phase, most of which were originated from the reagent degradation. Conclusively, Lix984N would degrade gradually during a long-term contact with the acidic aqueous feed and strip reagents. Lix84 and nonylphenol, as effective components of Lix984N, degraded almost completely after long-term recycling. As a result, the effective components of Lix984N were far lower in concentration than the dense-aromatic impurities derived from the diluent and the degradation products in total. The degradation of Lix984N would deteriorate solvent extraction, disengagement performance and result in more serious interfacial emulsion.

Jan 1, 2006

By David Dreisinger

The pressure oxidation of pyrite is an important hydrometallurgical technology, especially in the total oxidation of refractory gold ores and concentrates (gold is locked in the pyrite structure preventing direct cyanide recovery). It has been noticed in some commercial applications and benchscale studies that the leaching of pyrite may be slow and apparently can be inhibited by the presence of molten elemental sulfur in the leach pulp. The purpose of this study was to determine whether Ortho-Phenylene-Diamine (OPD) could be used as a surfactant or dispersant for sulfur in the pressure oxidation of pyrite. OPD has previously been shown to be useful for pressure leaching of zinc and copper sulfides at 150 C.In this work, the interfacial chemistry of sulfur was studied at temperatures of up to 190 C in the presence and absence of OPD and other surfactants. The contact angle between molten sulfur and pyrite was also measured. Finally, the impact of OPD on the kinetics of pyrite oxidation was measured in bench-scale pressure oxidation experiments. The essential finding of this study was that OPD lowers the interfacial tension between molten sulfur and acid solutions and increases the contact angle (reduces wetting) between molten sulfur and pyrite. The work of adhesion between sulfur and pyrite was reduced by more than an order of magnitude in the presence of OPD. In bench scale tests, addition of OPD was found to significantly accelerate the rate of oxidation of pyrite. Conveniently, it was found that OPD was also fully degraded during high temperature oxidation processes. No residual OPD was detected in solution or solid samples from the leach testing. OPD is recommended as a sulfur dispersant in the pressure oxidation of pyrite and/or elemental sulfur containing feeds.

Jan 1, 2003

"The pyrometallurgical method of recycling car batteries suffers from a potential for air pollution violations, which prompts the desire for a viable hydrometallurgicaJ alternative. Several Processes have been proposed, including leach-electrowinning routes using HBF4 and/or HzSiF6 based electrolytes, along with anodes of PbO2 on inert substrates.A study has been carried out to evaluate the proposed systems, with the intention of demonstrating a six month life of an electrolyte-anode combination. The work, which focused on the use of HzSiF6, has indicated that there was no acceptable anode, and has lead to the development of a technique to produce smooth, glassy, adherent coatings on graphite, and to the development of an anode composed of a series of copper cored graphite rods.The paper will present results on leaching and electrowinning experiments, as well as the description of a flowsheet for a pilot plant that will be used to produce one tone per day of refined lead from spent battery paste."

Jan 1, 1997

By R. Chiarizia

Third phase formation, i.e., the splitting of the organic phase in two layers, is a common feature observed, under conditions of high loading, for many solvent extraction systems of both analytical and industrial interest. Although this phenomenon has been investigated in a large number of works, a structural and physico-chemical description is still lacking. In this work, small-angle neutron scattering (SANS) data for the tri-n-butylphosphate (TBP)-n-octane,Th(NO3)4-HNO3 solvent extraction system have been interpreted using the Baxter model for hard-spheres with surface adhesion. The increase in scattering intensity in the low Q range, observed when increasing amounts of HNO3 and/or Th(NO3)4 are introduced into the organic phase, has been interpreted as arising from interactions between small reverse micelles containing three TBP molecules plus solutes in their polar core. This intermicellar attraction, under appropriate conditions, leads to third phase formation.

Jan 1, 2003

By Kimura. E.

Continuous estimation of phosphorus content of molten copper is required to produce phosphorus deoxidized copper in a continuous casting operation. The phosphorus content of molten copper was related to its electric resistivity, which was measured by the four-probed technique with a specially-shaped cell. In a laboratory scale, the linear relationship between the above factors was confirmed in the temperature range of 1083OC through 1200°C. The phosphorus concentration range measured was from 40 to 500 ppm. The phosphorus content was monitored successfully by measuring the electric resistivity of the molten copper in the distributor of a continuous caster in an industrial scale.

Jan 1, 1992

By Phillip B. Messersmith, Emmanuel P. Giannelis

"A versatile in-situ polymerization approach is described for the synthesis of polymerceramic nanocomposites consisting of two-dimensional layers of mica-type silicate (MTS) within polymer matrices. Functionalized, organically modified mica-type silicates (OMTS) were used to promote delamination/dispersion of the host layers and initiate polymerization of organic rrionomer. Epoxy nanocomposites prepared in this manner exhibit substantial modulus reinforcement at low silicate loadings. The water vapor permeability of the poly(?-caprolactone) nanocomposite containing 4.8% silicate by volume was reduced by nearly an order of magnitude compared to pure poly (?-caprolactone).IntroductionPolymer matrix nanocomposites are a relatively new class of materials with dimensions typically in the range of 1-100 nm.1 In general, because of the ultrafine phase dimensions involved, nanocomposites exhibit new and improved properties when compared to their micro- or macrocomposite counterparts. We as well as others are currently investigating the design, synthesis and characterization of polymer-ceramic nanocomposites. Our effort, in particular, has focused on the use of mica-type silicates (MTS) with various thermoplastic and thermosetting matrices.2-5MTS's belong to the general family of 2: 1 layered silicates. Their crystal structure consists of layers of two silica tetrahedral sheets fused to an edge-shared octahedral sheet of either aluminum or magnesium hydroxide. Stacking of the layers leads to a regular van der Waals gap or interlayer.6 Isomorphic substitution within the layers generates negative charges that are counterbalanced by cations residing in the interlayers. Although the natural forms of MTS's usually contain hydrated Na+ or K+ ions, ion exchange reactions with organic cations (e.g. alkylammonium ions) can render the normally hydrophilic MTS's organophilic."

Jan 1, 1994

By T. Kozuka, K. Sassa, S. Asai

"A new atomization process is developed. The principle of this process is completely different from that of conventional processes. This process uses electromagnetic energy induced by direct electric current and direct magnetic field instead of kinetic energy produced by fluid impingement or disk rotation.Experimental work of this process was carried out using pure tin, and it was found that the crucial factor for a stable operation is the contact state of molten metal with the electrode. In order to control the condition, a delay time controlling unit was developed and combined with this process. It is noticed that this controller works well to produce uniformly sized particles.A linear relation between the impulse and the momentum of atomized particles is found by use of experimental data and is explained by theoretical analysis.IntroductionIn atomization processes prevailing in metal powder technology, kinetic energy is currently employed for atomizing molten metal. That is, molten metal is broken into small particles by other fluid (e.g. water, argon gas, etc) or by impinged upon a rotating solid disk. This splashing process is always accompanied with uncertain factors for shape and size of the particles. The diameter distribution of products, therefore, comparatively spreads over a wide range. From another standpoint, the restriction of atmosphere is inevitable in some of these processes. As a pulverizing technology, the process which can produce uniformly sized particles and permits the choice of atmosphere is strongly desired.On the other hand, a great attention has been paid to the spray casting process as a new near net shape casting. In this process, a small size spraying device is favorable."

Jan 1, 1988

By M. Sahoo

The development of new alloys containing bismuth and selenium for potable water supplies are reviewed. The new alloys are replacements for the leaded red- and semi-red brasses by the low-lead alloys, SeBiLOYS I and II, for sand casting, and SeBiLOY III replaces the lead containing yellow brass, C85800, for permanent mold casting. As the new alloys use bismuth and selenium, the supply and demand of these elements are discussed. The key casting characteristics discussed are: tendency to dross formation, freezing range (liquidus and solidus temperatures), fluidity, resistance to hot tearing, microstructures, mechanical properties, machinability, grain refinement and corrosion behaviour.

Jan 1, 1999

By Wayne C. Stewart

Freezing of high pressure air lines and pneumatic equipment has been a recurring problem in the Thompson Smelter. The particular severity during the winter of 1989-90 resulted in costly process disruptions and repairs. A process improvement team with representatives from operations, engineering and both maintenance supervision and the shop floor was established to develop solutions. Their mandate included process evaluation, design, equipment and in-plant commissioning. In 1990, upon recommendation of the team, we installed three Refrigerant/Desiccant air dryers with a total capacity of 20,000 S.C.F.M. to service the Smelter. This paper discusses processes and process improvements associated with this installation.

Jan 1, 1993

By A. V. Tarasov, V. M. Paretsky

"The design is based on the thermal processing of the wastes in· the intensively bubbled melt in the Vanyukov furnace at the relatively high temperatures (1350- 1450 °C), In this case: -the secondary wastes are not formed; - the especially toxic substances at the outlet from the furnace are absent. The technology was tested on a large scale (on semicommersial bases). Technical and economical basis show profitability of recovery complex for processing of hard garbage waste (HGW) using this technology: the period of capital, investments refunding for the, recovery, complex construction with process annual capacity of 240 thousands tons of wastes is 1,5-2,5 years,"

Jan 1, 2000

By Glenn Stevens

After 40 years of operation with the original design, Pan Pacific Copper determined it was necessary to rebuild the Saganoseki Flash Smelting Furnace to continue safe operation. The original design employed a rigid steel frame, which, through hearth growth, led to severe distortion of the frame. Contributing to the continued growth of the hearth were thermal cycles that occurred during the government mandated annual shutdowns. Hatch designed a unique sprung bound, pivoting binding frame to maximize crucible size within the existing furnace footprint, while integrating the PPC designed cooling jackets. The bound system maintains tight brick joints, while the new conductive hearth design with integrated bottom cooling produces a protective freeze layer to accommodate higher furnace throughput. Minimization of furnace downtime for the rebuild was achieved through effective construction planning, highly trained contractors, and through an efficient start-up and ramp-up to full production.

By S. H. Castro

The El Teniente molybdenite plant (Chile), with a nominal capacity of 3,200 tpd of bulk Cu-Mo concentrate, produced approximately 3,385 metric tonnes of Mo during 1998 by using the phosphate Nokes process (LR-744 reagent). This is the only Chilean moly plant which traditionally has depressed copper and iron sulfides with LR 744 reagent, which is a hydrolysis product of P2S5 and NaOH. El Teniente's ore Mo grade is 0.02%Mo and is concentrated to 0.45%-0.50% Mo in bulk Cu-Mo flotation. Subsequently, molybdenite is floated by selective flotation to depress Cu and Fe sulfides, such as chalcopyrite, bornite, digenite and pyrite, to produce typically a 49%-50%Mo molybdenite concentrate. An optimisation program during the last two years was undertaken to improve molybdenite recoveries. Current molybdenite plant technology at El Teniente and use of phosphate Nokes in the process process is reported. Use of phosphate Nokes reagent has increased average Mo recovery from 70.5% in 1977 to a mean 74.7% for the first 4 months of 1999. The global Mo recovery, including bulk flotation, incresed from 42.3% in 1997 to 46.8% in 1998, with a projection of 55.5% for 1999. Mo production per year has increased from 3,181 tons in 1997 to 3,385 tons in 1998 and a projected 4,000 tons for 1999.

Jan 1, 1999

By Junji Shibata

The waste acid mixture whose main component is phosphoric acid, is discharged from the etching process in the liquid crystal production industry. In order to separate impurity acids from the phosphoric acid, trioctyl phosphate (TOP) is used as an extractant. TOP can extract acetic and nitric acids selectivity. The extraction and stripping operations are carried out for the acid mixture by beaker-scale experiments and countercurrent multistage operations with mixer-settler equipment. TOP selectively extracts the acetic and nitric acids in the acid mixture. From the results of the McCabe-Thiele analysis obtained by beaker-scale tests, the extraction for acetic and nitric acids are approximately 100%, respectively, by 6-stage extraction with a phase ratio (A/O) of 0.4. On the other hand, almost all of acetic and nitric acids are stripped with water from the organic phase by 4-stage stripping with a phase ratio (A/O) of 1.0. About 95% of acetic and 98% of nitric acids can be removed from the acid mixture without extracting phosphoric acid in case of the mixer-settler equipment operation. There are several steps such as slicing, lapping, chemical etching and mechanical polishing in the silicon wafer production process. The chemical etching step is necessary to remove any damaged layer caused in the slicing and lapping steps. The typical etching liquor is the acid mixture comprising nitric acid, acetic acid and hydrofluoric acid. The waste acid is treated by a neutralization method with a high alkali cost and balky solid residue. A solvent extraction method is applicable to separate and recover each acid. Acetic acid is first separated from the waste liquor using 2-ethlyhexyl alcohols as an extractant. Then, nitric acid is recovered using TBP (Tri-butyl phosphate). Finally hydrofluoric acid is separated with TBP solvent extraction. The expected recovered acids in this process are 2mol/L acetic acid, 6mol/L nitric acid and 6mol/L hydrofluoric acid. The yields of this process are almost 100% for acetic acid and nitric acid. On the other hand, it is important to recover and reuse the metal values contained in various industrial wastes from a viewpoint of environmental preservation. Most industrial products are made through processes to separate impurities in raw materials, solid and liquid wastes being necessarily discharged as industrial wastes. Chemical methods such as solvent extraction, ion exchange and membrane separation, and physical methods such as heavy media separation, magnetic separation and electrostatic separation are considered as the methods for separation and recovery of the metal values from the wastes. Some examples of the application of solvent extraction to the treatment of wastes such as Ni-Co alloy scrap, Sm-Co alloy scrap, fly ash and flue dust, and liquid wastes such as plating solution, the rinse solution, etching solution and pickling solution are introduced.

Jan 1, 2003

By Brian Lightfoot

Ausmelt Technology uses a furnace/slag/lance system in a way analogous to the way a chemical engineer would use a mixed reactor. The technology is sufficiently versatile to treat materials under a very wide range of temperature and chemical conditions. At one extreme the system has been operated at temperatures high enough and oxygen potentials low enough to make iron. At the other extreme it has been operated of temperatures as low as 800°C and oxygen potentials high enough to cupel lead from silver. This versatility permits the treatment of a great variety of wastes including asbestos, mixed organic\heavy metal wastes, incinerator ash smelter residues, waste water treatment sludges, organochlorine compounds and many others.

Jan 1, 1994

By S. Kurama

Incorporation of de-watering sieve waste of borax (TSW) from Etibor Kirka Borax Company (Turkey) on the mechanical and physical properties of a commercial floor tile composition was investigated. In order to achieve this aim, TSW was partially employed in place of feldspar in the standard composition up to 20 wt %. The formulated compositions were wet milled, dried, shaped and then fired at 1190C for a total firing time of 38 minutes (from cold to cold) under industrial conditions. It was found that using of TSW up to 15 wt % improved the physical and mechanical properties of final product. The results indicated a good prospect for TSW as a co-flux in floor tile formulations.

Jan 1, 2006

By Yotamu Stephen Rainford Hara

"The study focuses on the reduction mechanisms of copper, cobalt and iron during carbothermic reduction of copper-cobalt mineral sulphide concentrates in the presence of lime, in the temperature range of 1073K and 1273K. We have used three types of mineral concentrates which were derived from froth flotation from the Copperbelt region in Zambia. The reduction mechanisms were studied using thermogravimetric analysis in which selected reactions were stopped at different times for characterising the reaction mechanism using optical microscopy, XRD and SEM-EDX analyses. Using SEM-EDX analysis, we have analysed in details the stages of metallic phase formation during reduction process. Metallic cobalt and iron were embedded into copper, thereby permitting magnetic separation of the reduced metals even though copper is diamagnetic. Methods of preferential reduction of metal values were investigated by analysing the metallic phase formation.IntroductionIn conventional smelting or converting of copper sulphide minerals, metallic copper forms by giving off S02 gas on. Although in terms of overall energy balance the selective oxidation for metal production has major advantages, the process suffers from drawbacks in smelting complex concentrates containing copper, cobalt and iron sulphides minerals and these are: (i) cobalt and iron are oxidised, and consequently cobalt is lost into the slag phase. (ii) The volume of S02 gas produced is in low concentrations, which is insufficient for extracting sulphur or manufacturing sulphuric acid. The release of dilute S02 causes serious environmental pollution. The major cause for the loss of cobalt and iron into the slag, is due to that fact that the oxides of these metals are more stable than their sulphides. Since cobalt and copper are more valuable than iron, reducing conditions are required in a separate slag treatment reactor using electric arc melting for recovering the lost metal oxides from slag. This energy-intensive step makes metal making expensive.During chemical beneficiation of mineral sulphides (Cu2S, CoS, FeS) in the presence oflime (CaO), two types of equilibrium conditions may be set up either by forming CaS under reducing conditions, or by stabilizing CaS04 under oxidising conditions [l]. By comparison in the presence of carbon, CaS and metallic phases form, enabling the recovery of metals from sulphide minerals, which have been investigated by a number of authors [2-9]. During reduction of metal sulphide in the presence of lime and with carbon, it has been proven that the overall reaction le proceeds via two main steps: [5, 8, 9] (i) the anion exchange reaction between metal sulphides (MS) and CaO as shown in equation la, followed by (ii) the reduction of metal oxide (MO) via reaction lb."

Jan 1, 2013

By Rudolf Keller

In the electrolysis of neodymium oxide from a molten fluoride electrolyte, anode effects may occur at the carbon anodes, interfering with smooth cell operation. In laboratory experiments, we attempted to circumvent this problem by selecting electrolytes with a high oxide concentration, possibly at relatively low rare earth content, but cathodic deposition was not satisfactory. A regime at higher cell voltage was discovered to yield good cell performance, but evolution of considerable amounts of fluorocarbon compounds suggested that a reactive treatment of the off-gases would be necessary for environmental acceptability. Subsequent experimentation at low cell voltage revealed conditions for satisfactory operation without occurrence of anode effects and without formation of any CF4 or C2F8.

Jan 1, 1997

By Seshadri Seetharaman, Nurni N. Viswanathan, Haijuan Wang

"In order to make the stainless steel making process efficient and environment friendly, it is essential to minimize the loss of chromium to the slag phase. With a view to investigate the advantages of using CO2 to attain moderate oxygen partial pressures in the oxidant gas during the decarburizations of stainless steel, the present experiments were carried out to understand the oxidation kinetics of Fe-Cr alloys and Fe-V alloy with gas mixtures containing CO2. In the present work, the oxidation behavior of Fe-Cr and Fe-V was examined by thermogravimetric analysis (TGA). Various mixtures of O2 and CO2 were used as the oxidant gas and the oxidation rate was followed by the weight changes as a function of time.The experiments demonstrated that the oxidation rate is independent of temperature at present experimental situation, but has strongly related to the Cr-content of the alloy as well as the oxygen partial pressure in the oxidant gas mixture. The wetting of alumina by the iron drop and the change of the drop shape during the course of the oxidation were investigated by X-ray radiography."

Jan 1, 2010