Search Documents

By A. M. Alfantazi, M. Boissoneault, D. B. Dreisinger, J. Synnott

"The effects of five commercially available foaming reagents (range of 0 to 25 ppm) namely Dowfroth 250, Saponin, Yucca, Licorice and Meta-Para Cresol on acid mist control, current efficiency, polarization behavior, and deposit morphology and orientation were investigated. The deposition was carried out using a bench scale electrolysis apparatus (cell volume 3L) at 500 Nm-2 and 38°C for 3 hours from Kidd Creek zinc electrolyte. The acid mist control capability of the various reagents was studied and compared by characterizing the foam layer generated during actual electrowinning conditions and by direct quantitative measurements of acid mist levels on top of the electrowinning cells. Within the range considered, the addition of these reagents reduced the current efficiency, refined the grain size of the deposit, and changed to preferred orientation of most of the deposits. Among the reagents tested, acid mist measurements indicated that Licorice and Dowfroth 250 were the best acid mist suppressant at emissions of 0.30 mglm3 and 031 mg/m3 respectively while Yucca and MPC produced the most mist at 3.0 mg/m3 and 33 mg/m3 emission rates, respectively.IntroductionMost of the world's primary zinc is produced via a combined roast-Ieach-purificationelectrowinning process. Depending on the electrolysis conditions, several additives may be added to the electrolyte. Some (e.g. glue, antimony, sodium carbonate) are added to mainly counteract the detrimental effects caused by impurities while others (e.g. licorice, Saponin) are used as foaming reagents to prevent excessive acid mist formation. Acid mist emission is a problem in many electrolysis operations because it corrodes the equipment and is a health hazard to the workers in the tankhouse as well as it pollutes the environment. Due to recent trends towards more environmental protection and more stringent in-plant hygiene, there is an increasing need to minimize these aerosols. In order to eliminate or minimize these aerosols foaming agents are usually added to the electrolyte to produce a foam layer on top of the electrolyte, thus trapping most of the mist. The ideal foaming agent would trap all of the mist and would not interfere with the electrowinning process. It is also evident that the reagent toxicology, cost and availability are important factors that need to be considered.Review of the available literature clearly indicated that very little work has been done in the past on the subject of acid mist control in electrowinning operations particularly in the area of foaming and anti-misting properties of surfactants. Two papers [1,2] have reviewed briefly the existing technologies for acid mist control. Recently, most of the work in this area has focused on the development of special mechanical devices that could be attached to the electrodes and control the mist generation at the source before it is emitted to the cellhouse [2-5]. On the other hand, extensive body of literature exists that deals with the effects of anti-misting reagents on the electrowinning aspects [6-7]."

Jan 1, 1997

By Erich Hovestädt, Hans-Jürgen Odenthal, Christian Wuppermann, Herbert Pfeifer, Antje Rückert

"During the argon oxygen decarburization (AOD) process high-chromium steel melts are decarburized by oxygen and inert gas injection through sidewall nozzles and a top-lance. Due to the large amount of the injected processing gas, low frequency oscillations of the vessel can be observed. It is suspected that these oscillations can influence the converter's structure. The exchange of forces between fluid and the surrounding vessel is the focus of this study. An oscillation model was developed and tested, one objective being to limit the computational effort which is necessary for fully coupled and time resolved CFD and FEM simulations. Experimental results obtained from water-model studies as well as from on-sight measurements are available and were used in order to validate the numerical results. The authors' intention is a contribution towards a more in depth understanding of the factors influencing vessel vibration during the AOD process.IntroductionDuring the last four decades the AOD process has been established as a reliable and efficient refining process in stainless steel making. The injection of process gases (O2, N2, Ar) through sidewall nozzles shows advantages in mixing effectiveness compared to other injection geometries e.g. bottom blowing [1]. Stainless steel grades contain usually more than 10% chromium. With decreasing carbon content during the decarburization periods the tendency of chromium oxidation increases according to the varying chemical equilibrium which depends on the partial pressure of carbon-monoxide (CO) in the gas phase. That's why oxygen is gradually replaced by inert gases, usually argon or nitrogen, in order to lower the CO partial pressure and thus to minimize chromium oxidation. Despite the high injection velocity of approximately Ma = 1, the kinetic energy of the gas jets is consumed within a short distance from the nozzle exits due to the large density ratio between gas and melt of approximately 1:8000. With increasing distance to the nozzle exit, the initial horizontal velocity of the gas jet decreases and due to buoyancy force motion of the detached bubbles turns into a vertical direction. Subsequently a gas plume develops with its typical conical shape described by various authors [1-4]. Due to the drag force between gas bubbles and melt also the liquid phase is forced into a vertical motion. Near the free surface and the wall regions the melt flow is deflected in different directions. Subsequently, the typical flow pattern in the AOD vessel arises, as sketched in Figure 1 and described in literature [5-9]."

Jan 1, 2012

By Ledjane Barreto, Tulio Flávio Accioly de Lima e Moura, Wilson Acchar, Antonio Carlos Silva da Costal

"Clays are common ingredients in pharmaceutical products both as exclplents and active substances. Clay minerals are naturally cationic exchangers and they may undergo ion exchange with basic drugs in solution. Smectites, and montmorillonite have been studied due their high cation exchange capacity as compared to other silicates. Recently a patented study reports the use of attapulgite as the encapsulating agents both for the protecting the active substance and modulating release into the body. Some clays such as kaolinite, smectites, talc, etc are also used as dermatological protectors. Sepiolite and smectites have the ability to form complexes with organic compounds with absorb ultra-violet radiation, enabling them to be used in sun screens with protection factors. The objective of this work is to characterize the attapulgite in order to study the potential use of this clay material in the human health.IntroductionSince the begimling of time, nature has served humanity as a source of various raw materials. Among these, clays such as kaolinite and ilitte are common ingredients in the tile production. Recently, special clay materials have been investigated in order to identifY new potential uses of these class of materials. Clay materials are natural raw material and have excellent properties such as low toxicity, good biocompatibility, making them a good material to be used in biological applications. Attapulgite (paligorskite) and sepiolite is so called special clays. These special clay materials are very sin1ilar and have a great potential to be used in some technological areas due their special catalytic, sorptive and colloidal-rheological properties [1-8]. Recently some works have reported the use of these special clays materials for many applications such as drug delivery, wound dressing, oil absorbent, pesticides, fertilizers [9-12]. Brazil has a significant reserve of attapulgite located in Piaui state, making the study of the potential of this mineral in special areas, very attractive. Attapulgite is classified a fibrous alluminous silicate material and shows the presence of micro pores and channels, fine particle size and high surface area making this material a good candidate alternative material to be used in many industrial applications [6,8,9,11,12]. The objective of this work is to characterize the physical and microstructure of attapulgite."

Jan 1, 2012

By José Antonio, Silva Souza, Luis Alves Venancio, Emanuel Negrão Macedo, Antonio Ernandes M. Paiva

"The production of alumina from bauxite using the Bayer process generate 1.25 ton of the residue known by red mud and 460 kg of CO2 per ton of alumina.The direct use of exhaust gases from the alumina refineries to react and neutralize the bauxite residue may allow a double gain: open a wide range of new applications for bauxite residue reducing the reactivity of red mud and sequester approximately 15% or 67 kg of CO2 per ton of alumina.This paper shows the reaction of a suspension of bauxite residue-water with a simulation of the calcinator exhaust gases of the refinery. The influence of the temperature and the ratio water red mud is also analyzed.2 IntroductionThe production of millions of tons per year of alumina around the world generates around 1.25 tones of the residue known as red mud and 0.4 ton of CO2 per ton of alumina . The vast majority of the red mud is stored in large sealed lakes. Due to the high reactivity is considered dangerous and currently there is no operating process capable of reuse all the material at any refinery. These lakes after filled of solid material eventually have the surface revegetated. Otherwise will need monitoring for decades and remain as an environmental passive. The search of a industrial process that combine the reduction of the CO2 emission and the reduction the pH of the red mud opening the possibility of use in large scale in a economically viable way is the main objective of this work.The use of the exhaust gases of the refineries to neutralize the bauxite residue may allow a double gain: Open a large array of new applications for the residue with the reduction of its reactivity and sequester million of tones of CO2 plus other gases like SO2 [7] and NOx.This project main objective is to study the reaction of the CO2 with the Bayer process residue in order to obtain the basic parameters to design an equipment capable of process this reaction on a pilot scale. With this objective compositions of red mud on spray were processed with flow of gas containing CO2 at different temperatures and with concentration similar to the exhaust gases of the calcination process of the refineries. With the results, basic concepts of a pilot scale equipment were evaluated.A revision of the work already done on this type of residue were done [3, 9, 10]. Alternatives and potential barriers on chemistry and environmental fields were discussed. With the objective of industrial application the potential use of these materials were evaluated through the pH control, mass balance and x-ray diffraction."

Jan 1, 2010

By James Vaughan

Ionic liquids are solvents of interest for applications such as electro- plating, winning and refining of metals. Of particular interest is the possibility of processing reactive metals such as aluminium, magnesium and titanium that cannot be deposited from aqueous solutions. Aluminium has been electro deposited from AlCl3 : ionic liquid mixtures at low temperatures relative to conventional Hall-Héroult smelting. Imidazolium ionic liquids are have been used in the past due to their relatively high ionic conductivity and cation stability. The less studied and less expensive phosphonium ionic liquids systems may provide a viable alternative to imidazolium ionic liquids for certain applications. New information regarding the physical properties and electrochemical behaviour of phosphonium ionic liquid systems is presented.

Jan 1, 2006

By Bo Björkman

Four different arsenic containing dusts from the Boliden plant, Boliden mineral AB, Sweden have been examined. A kinetic study of the As elimination was performed in a laboratory scale roasting furnace for roasting furnace ESP dust and smelting furnace ESP dust. Characterisation and thermodynamic calculations were carried out to determine the mineralogy, and the stability of compounds in the dusts studied. The characterisation methods used were chemical analysis, X-ray diffraction analysis and microprobe analysis. It was found in the experiments that a high degree of As elimination was obtained for roasting fumace ESP dust and a low degree for smelting fumace ESP dust. Derived kinetic models are given. A prediction of the As-elimation for settling furnace dust and converter ventilation dust is presented.

Jan 1, 1994

By Shoji Taniguchi, Lifeng Zhang, Kaike Cai

"In the present paper, based on the two-phase (Eulerian-Eulerian) model, the 3D fluid flows in gas-stirred systems, i.e., air-stirred water vessel and argon-stirred liquid steel ladle, are simulated. In the Eulerian-Eulerian two-phase model, gas and liquid are considered to be two different continuous fields. The phases are assumed to share space in proportion to their volume fractions. The exchange between the phases is represented by source terms in conversation equations. Turbulence simulated by the k- e model is assumed to be the property of the liquid phase. The following effects of mathematical treatments and operational factors on the fluid flow are discussed, such as interphase drag force, turbulent model, the size of bubble, and gas injection mode.Some interesting results are derived. Except the interphase drag force, the interphase lift force should be taken into accounted in order to exactly simulate the fluid flow in gas-stirred systems. Suitable turbulent model and drag coefficient have effect on the mathematical simulation. Injecting small bubbles can realize a well mixing flow condition. The distance between the two gas-injection nozzles has effect on the fluid flow."

Jan 1, 2000

By E. Ilgar

"Deposition studies were conducted in acid copper electrolyte to determine the influence of chloride ions on cathode morphology. A statistically designed screening test was carried out in the absence and presence of 20 ppm CI- using a three factor, two level factorial design, in an electrolyte containing 36 gl'! Cu2+ and 150 gl-! H2S04, The independent variables evaluated were agitation; current density and temperature and their influence on surface roughness was determined. The copper deposited at current densities where activation was the primary control mechanism appeared similar in morphology whether stirring was used or not. The addition of 20 ppm CI- to the electrolyte gave rougher deposits under the same conditions. In the mixed control regions, considerably rougher, dendritic deposits were obtained when CI- was present. Agitation was effective in reducing the copper surface roughness both in the apparent activation and mixed control regions in the presence ofCI-. The results of this study showed that 20 ppm Cl- polarized the copper deposition at low overpotentials but caused depolarization at higher overpotentials.IntroductionChloride ion is inherently present in copper electrolyte, either as an additive or from other sources such as make up water. The behavior of the chloride ion is well documented in electrorefining operations, but its role in copper winning is less obvious. However in both cases there is evidence that cathode growth and solution chemistry are strongly influenced by its presence. The mechanism and electrochemical action of the Cl"" have been shown to be very complex, therefore a better understanding of its influence on electrocrystallization is essential for improved cathode deposit growth control. It was proposed that Cl"" polarizes the copper deposition reaction at low concentrations due to CuCI formation but depolarization occurs at higher concentrations due to the formation of a soluble CuCI2"" complex [1,2]. Franklin [3] reviewed the mechanism of additives in the electrodeposition process and proposed that the Cl"" complexed with copper, adsorbed on the cathode as an induced anion leading to an increase in the reduction rate. At cathodic overpotentials less than 100 mY, lppm NaCl had a polarizing effect, i.e. an increase in impedance of the charge transfer step. At higher Cl"" concentrations up to 100 ppm, depolarization occurred as evidenced by a decrease in impedance, which was attributed to soluble cuprous complexes [4]."

Jan 1, 1997

By Jianxun Song, Hongmin Zhu, Qiuyu Wang, Jungang Hou, Shuqiang Jiao, Xiaobo Zhu

This work presents the results of a study on the Ti3+/Ti2+ couple redox potentials vs. Cl–/Cl2 at the temperature range (673 to 1073 K) in fused LiCl-KCl eutectic by direct potentiometric method. Initial concentrations of TiClx in solvents did not exceed 5.0 mol%. Basic thermodynamic properties of the reactions TiCl2+1/2Cl2(g)=TiCl3 were calculated using the temperature dependencies of apparent standard potentials of the couples E* Ti3+ /Ti2+.

Jan 1, 2014

By Z. Zak Fang, P. Fan, S. Middlemas

"Titanium dioxide (T1O2) has been widely used as pigment in paints, paper and cosmetic products, as well as high-tech applications such as PV Cells, semiconductors, biomedical devices and air purification. T1O2 pigment is primarily produced by the high temperature chloride process, resulting in considerable CO2 emissions. A novel hydrometallurgical process for making T1O2 pigment without direct CO2 emission is investigated. The new method promises to eliminate direct CO2 emissions, consume significantly less energy, and produce minimal environmental waste. The novel process involves molten salt roasting of titania slag, with subsequent washing, leaching, solution purification, hydrolysis, calcination and post-treatment stages, resulting in high-purity anatase or rutile pigments while realizing significantly reduced environmental impacts. Pigment whiteness is critically sensitive to trace amounts of discoloring impurities such as iron and chromium. Several methods for reducing the levels of these impurities are investigated. Energy consumption and emission models are also developed.IntroductionTitanium dioxide (T1O2) is one of the most commonly used minerals in the chemical manufacturing industry. It has been commercially processed since the early 1900's, and has a wide variety of applications. Pigment is used in paints [1], plastics and paper [2], sunscreen [3], cosmetics and even as a food additive [4]. T1O2 has also been used in photovoltaic cells [5], biomedical devices [6], and in air purification [7]. T1O2 pigment has a refractive index of 2.7, which imparts a high level of opacity (and hence whiteness) to whatever material it is added [8]."

Jan 1, 2012

By Xiao Yang

Calcium oxide is one of the major fluxing agents used for steel refining. Because unreacted CaO remains in slag in most cases, discharged slag is difficult to be recycled smoothly. With the growth of environmental concerns, improving utilization efficiency of CaO is required to reduce the amount of discharged slag and energy consumption. The authors have reported a resource and energy-saving process by using multi-phase flux for dephosphorization. Reaction behavior of phosphorus in multi-phase CaO–FeOX–SiO2–P2O5 flux system was investigated. Formation mechanism of P2O5-rich phases was clarified at the interface between solid CaO or 2CaO, SiO2 and molten CaO–FeOx–SiO2–P2O5 slag. Phase relationship and thermodynamic properties of 2CaO, SiO2-3CaO, P2O5 solid solution were observed to confirm the condensation of P2O5 in solid phase. Based on these results, reduction of CaO consumption, discharged slag curtailment, and energy-saving effects in the novel refining process by using multi-phase flux were discussed.

By Alana Pereira Ramos, Walman Benicio de Castro

Amorphization and martensitic transformation (Ms) characteristics of Ti–Ni-Cu alloy ribbons prepared by melt spinning were investigated by means of differential scanning calorimetry and X-ray diffraction. In these experiments particular attention has been paid to change the wheel linear velocity from 21 to 63 m/s. Then the cooling rates of ribbons were controlled. The effect of this cooling rate and alloy composition on martensitic transformation behavior is discussed.

Jan 1, 2015

By Hongmin Zhu, Suning Liu, Kai Huang

"Recovery of silicon particles from the cutting slurry for the manufacturing of solar grade silicon is very important to recycle this kind of special resource. The challenge is to separate the silicon particles from the mixed abrasive particles which contain SiC. Various methods such as sedimentation, centrifugation, and flotation have been conducted, while in present work, a simple and effective novel method was proposed to study the separation of Si and coexisting SiC particles in the cutting slurry. The new process is based on the size difference between the two kinds of microparticles. And the membranes with the different pore sizes of 1µm, 2µm, 3µm and 5µm were used to test the pass ratio and separation efficiency of the suspension. Results shows that the effective separation of Si and SiC microparticles was obtained under the optimal conditions, and indicating great potential of practical enrichment of Si from the coexisting abrasive particles.IntroductionWith the development of the world economy, energy shortage and environment problem is becoming more and more seriously. Solar energy, which is regarded as one of the most important new energy in the word, has received much attention and interest from the scientists [1, 2]. More than 80% solar cells are manufactured by the high purity polysilicon as the raw material. The main process of producing silicon wafer is by multi-wire slicing. In this slice processing, large amount of slurry is produced. The slurry contains more than 30% wt silicon powder, silicon carbide powder as the abrasive, scraps of metal chips, as well as cutting abrasive suspension polyethylene glycol (PEG). The high-purified silicon powders are worth recycling and reusing as the materials for preparing solar-grade silicon though it is a big challenge [3].Most of the current studies were focusing on the recycling of the silicon carbide and PEG, while work on the recycling of the high-purified silicon is not so been focused since there is lacking of very effective separation and recovery technologies till up now. Nishijima utilized the method of superconducting magnetic to recycle the abrasive [4]. Wang applied a combinational process of chemical treatment, high-gravity centrifugation, high-temperature precipitation technique and directional solidification to enrich the silicon [5]. And other purification methods, such as centrifugation [6], froth flotation technologies [7], electrical filed separation [8] and phase-transfer process [9] have been employed. The disadvantages such as using poisonous media or complex equipments decrease the feasibility and efficiency of the above mentioned techniques."

Jan 1, 2014

By Seung-Chul Lee

Transparent conducting tin(1V) oxide thin films have been studies and developed for the electrode materials of solar cell substrate. Fabrication of tin oxide thin films by sol-gel method is process development of lower cost photovoltaic solar cell system. The research is focused on the establishment of process condition and development of precursor. The precursor solution was made of tin isopropoxide dissolved in isopropyl alcohol. The hydrolysis rate was controlled by addition of triethanolamine. Dip and spin coating technique were applied to coat tin oxide on borosilicate glass. The resistivity of the thin film was lower than 0.18-cm and the transmittance is higher than 90% in a visible range.

Jan 1, 1999

By J. G. Peacey, P. Hancock, R. -Q. Li

A pyrometallurgical process for the direct recovery of zinc from zinc concentrates and zinc/iron residues has been proposed and tested extensively by Noranda. The process consists of smelting bone-dry zinc containing materials (sulfide concentrates and secondary zinc/iron materials) in a molten iron oxysulfide bath to volatilize metallic zinc into a SC^-free offgas. Sulfur contained in the feed materials is fixed as an iron oxysulfide matte for disposal. Thus, this process not only is capable of treating zinc sulfide concentrates and secondary zinc materials simultaneously, but also eliminates the need of sulfuric acid production. Detailed thermodynamic analysis and experimental test work are described in this paper.

Jan 1, 2000

By Uday B. Pal

In the electrochemical vapor deposition (EVD) process, gaseous cation precursors are passed over one side of a porous substrate, and oxygen is passed on the other side of the substrate. The gases diffuse and react within the porous substrate, and the pores get filled with the desired solid oxide. Subsequent solid state electrochemical transport through the solid oxide in the pores continues the reaction, and the film grows over the porous substrate. The EVD process has been used to deposit lanthanum chromite interconnection films and yttria stabilized zirconia electrolyte films over porous air electrodes. The EVD growth of these solid oxide films is found to be parabolic in nature, which indicates that the solid state transport (diffusion) of ions through the film controls the growth. This solid state transport can be analyzed using Wagner's treatment of the electrochemical transport. Conductivity measurements and the information on the defect structure of the oxide can be combined with the EVD growth rate measurements to calculate the solid state transport properties (transport numbers and partial conductivities) of the rate-controlling minority species in the oxide. Using this approach, the EVD growth of other electronic, mixed conducting and ionic solid oxide films can also be analyzed.

Jan 1, 1992

By Tan Pengfu

By using computer-aided techniques of equilibrium calculations for multicomponent and multiphase systems, a computer model has been developed to simulate QSL, KIVCET and Outokumpu flash lead smelting processes. A mathematical description is studied using two zones or three zones, namely smelting zone and slag reduction zone for QSL furnace, or offtake shaft zone, smelting shaft zone and electric furnace zone for KIVCET furnace. The amount of each component in lead, slag and gaseous phases under equilibrium is calculated by using the data of free energies of formation and activity coefficients. The predictions by the present computer model are compared with the known data from QSL-Plant at Korea Zinc Co. in Korea, KIVCET-Plant at Nuova Samim Co. in Italy and Outokumpu Co. in Finland. The agreements between the computer predictions and the known data are excellent, so that the present computer model can be used to monitor and optimize the actual industrial operations of direct lead smelting.

Jan 1, 1998

By J. Huisman

With the introduction of ever-stricter environmental operating guidelines, capital expenditure restrictions and operational budget cutbacks, the biological method of SO2 removal becomes more and more attractive. Biological treatment of dilute flue gases is a more cost effective technology in comparison to conventional sodium hydroxide scrubbing. Although the investment costs for sodium hydroxide scrubbing is lower, the operational costs are significantly higher. In addition, the end product of the biological installation is sulfur instead of sodium sulfate; and no further wastewater treatment of the bleed from the biological installation is required since heavy metals are removed simultaneously. Another option for the treatment of SO2 containing gas at a sulfuric acid plant is the production of extra sulfuric acid of the discharged SO2 by applying an additional converter. Comparing biological treatment with this option shows much lower investment costs for the biological installation. Sulfur is produced which can be converted to sulfuric acid, so the bio-route will be more cost-effective than an additional converter. In principle, the biotechnological gas cleaning system is an integration of an absorber with a wastewater treatment facility. In the absorber, the SO2 containing gas is brought into contact with the washing water. The effluent absorber liquid contains a mixture of sulfite and sulfate that is converted into elemental sulfur. This conversion takes place in an integrated system; first, the sulfite/sulfate mixture is converted anaerobically into sulfide; secondly, the sulfide is converted aerobically into elemental sulfur. Subsequently the sulfur is separated and the water is returned to the absorber. Due to the buffer capacity of the washing water, removal efficiencies over 98% are possible. In addition to SO2 removal, it is possible to convert for example other bleeds streams such as scrubber acid or weak acid to sulfur in the same SO2 installation. Recent evaluations concluded that biological desulphurization of flue gases is not only economically attractive in comparison to convention sodium hydroxide scrubbing but also in comparison to gypsum producing systems and even seawater scrubbers. This paper describes the technological and economical viability of biological flue gas desulphurization.

Jan 1, 2005

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 F. Ríos

Fundamental research, at laboratory scale, on the biomass adsorption capacity of a liquid mining effluent has been done. The biomass used corresponds to a Chilean seaweed called Gracilaria chilensis. The waste water effluent corresponds to clear water coming from thickeners of a Chilean copper mining operation. The biomass was dried, washed, treated with an acid solution, and then reduced in size. A characterization of Zeta potential was made, finding negative values in a wide pH range with a ZPC equal to 2.5 1. Adsorption tests were made- in an agitated system containing an artificial solution of CuS04 at a controlled temperature of 25 degrees Celsius; also, the effect of pH over the copper adsorbed was studied. Maximal adsorption of copper was found at pH equal to 6, and the Langmuir model indicated values for saturation of 52.08 mg/g and for standard free energy of about -21 KJ/mol. Kinetic adsorption was very high and fitted very well with a second order model equation, finding that 90 per cent of the adsorption occurred during the initial 10 minutes. After stoichiometric when 1 mol of copper is adsorbed, 2 mol hydrogen are released, showing that the main mechanism to remove heavy metals is the ionic exchange, and the seaweed ensures total discharge of copper adsorbed when the pH value is about 1. Experiments done with real waste water from thickeners lead us to conclude that optimal results for copper and molybdenum adsorption are at pH around 3.25 and the remaining treated water may be partially discharged into the water currents, thus showing that Gracilaria chilensis can be used to remove heavy metals easily from liquid effluents in the copper mining industry.

Jan 1, 1999