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By M. I. Zinigrad

A model of an ideal associated solution is presented. This model takes into account the existence of complexes of various compositions, sizes and geometries and allows calculating thermodynamic properties and phase diagrams of binary alloys. The model has been used formerly to calculate thermodynamic parameters and the position of the liquidus line for binary eutectic systems and also those having a stable compound in the solid phase. In all the cases the model parameters were not adjusted rather estimated from melting temperatures of the components. The recent studies dealt with the influence of arbitrary-stoichiometry associates on the equilibrium thermodynamic properties of liquid alloys. The application of the model to eutectic systems and systems having an unlimited solubility in solid and liquid states close to liquidus has been considered. It was shown that if the difference in melting temperatures of the components was small, different types of fusibility diagrams were possible: eutectic diagrams, cigar-shaped diagrams or diagrams with upper or lower azeotropic points. Peritectic transformations could take place when the difference in melting temperatures of the components was large. The present work is devoted to calculation of phase diagrams and thermodynamic properties of binary systems on the basis of chrome.

Jan 1, 2006

By Ho-Jung Shin

The influence of cooling rate from 1873 to 1473 K on the size and morphology of austenite grains was studied using a Fe-O.I5 % C-I.5 % Mn alloy. The experiments were carried out at three different cooling rates of O.33KJsec, O.67KJsec and air-cooling. The austenite grain showed an isotropy at 0.33KJsec but maximized anisotropy at O.67KJsec and become much less. anisotropic. In order to account for these phenomena, a model was developed for estimating the size and morphology of austenite grains as a function of cooling rate. The driving force for the )( phase formation from 0 phase is caused by undercooling degree due to cooling rate and energy barrier is restricted to the misfit strain energy which is caused by mismatch between )( phase and 0 phase. The )( phase from 0 phase could be formed on not random orientation index systems but specific orientation systems depending on cooling rate.

Jan 1, 2001

By Sergio N. Monteiro

Polymeric matrix composites reinforced with coir fibers are being used in many industrial applications such as automobile interior panels and cushions. These composites have relatively low mechanical strength due to the weak fiber/matrix interface. The objective of the present work was to investigate the effect of a surface alkali treatment of the curaua fiber on the mechanical behavior of polyester composites with different amounts of these fibers. The treatment, also known as mercerization, was performed with distinct concentrations, 0.1 and 10% of NaOH at 1 min and 1 hour, before incorporation of the coir fibers into the polyester composite. The results showed no significant change in comparison to similar untreated coir fiber composites. A microstructure analysis revealed that, in addition to reducing the hydrophilic characteristic of the fiber,the treatment also affects the surface morphology and impairs the fiber/matrix interfacial strength.

Jan 1, 2009

By Daniel C. McLean

Extraction data for Cu, Zn and Fe were obtained from 4.5" and 10" columns using massive sulfide ore and natural acid mine water. The purpose was to determine if recycling of solution through the column would produce leach liquors of 4 g/l Cu and Zn at extraction rates of 1 g/l per pass at typical flow rates of 0.002 to 0.006 gpm/sq.ft. Test results exceeded expectations. Cu and Zn concentrations of 4 g/l were obtrained within 4 to 6 cycles. Concentrations greater than 6 g/l Cu and 8 g/l Zn were reached within 10 cycles. Concentrations of greater than 40 g/l of Fe and free sulfuric acid were obtained with no decrease in biological activity being observed. No reagents were used.

Jan 1, 1995

By M. E. Ramos Rada

Mexicana de Cobre, which is part of Grupo Mexico, carried out studies for the construction of a copper refinery in the La Caridad Metallurgical Complex located in Nacozari, in the state of Sonora, Mexico. After the studies were concluded, the decision was made to construct a 180,000 t/y refinery using the state of the art permanent cathode Kidd Process. The basic engineering was developed by Fluor Daniel and the detail engineering and the construction were carried out in record time by the Mexican company Bufete Industrial. During the construction phase, Grupo Mexico decided to expand the refinery, and actions were taken to increase its capacity by an additional 120,000 t/y; the final result was a refinery capable of producing 300,000 tonnes of grade A cathode per year. Construction began in January 1996, and the operation of the first stage began on July 1, 1997. The operation of the second stage commenced on January 7, 1998. The capacity of the first stage was reached in November, 1997 and the total capacity of the refinery was achieved in May, 1998. This presentation describes the process and equipment installed in the refinery, the steps leading to the start-up, the operation and the results obtained during the first two years, the handling of anodes with high impurity contents, and the problems confronted and the way they have been solved. It also includes personnel productivity, the control parameters and the most relevant data on the operation of the process.

Jan 1, 1999

By XUEWEN WANG, Xingming Wang, Xuehui Liu, Mingyu Wang

The Panzhihua titanium concentrate contains high contents impurity of Mg and Al, and it is difficult to prepare high grade titanium slag. To solve this problem, a sodium salt roasting-acid leaching process was proposed for removing the impurities in titanium concentrate. Na2CO3 and titanium concentrate were mixed with the proportion of 1:4, and then the mixture was roasted at 700 for 2h. After roasting, the calcine was leached with HCl solution. The experimental results showed that the removal rate of silicon and aluminum can reach more than 85% and 80%, respectively, at leaching temperature of 70 , leaching time of 4h, HCl addition of 5ml and liquid-solid ratio of 4:1.

Jan 1, 2016

By Mark R. Jolly, Jean-Christophe Gebelin, Aleksander Cendrowicz

"Injection of wax patterns is the first stage of the multi-stage process of investment casting. The quality of the final casting and its dimensional accuracy is highly dependent on this stage of the process. Pattern waxes used in the industry behave in a complex visco-elastic-plastic manner. The modelling of such material behaviour is therefore not simple.In this paper a number of configurations of die will be shown in which the injection of the wax has been carried out for a range of processing conditions. Some of the dies are transparent and the movements of wax front observed can be compared with those predicted by simulation. Surface defects in final components will also be shown and compared with the location predicted by simulation software. Some discussion will be presented on the limitations of the software used and the time-scales achieved for practical use as a design tool within the foundry environment. IntroductionThis paper presents the research activities carried out at the University of Birmingham on the modelling and prediction of the behaviour of industrial investment casting waxes during the injection of wax patterns. These research activities are done in the context of a more global study of the fundamental aspects of the investment casting process, the FOCAST project. Regarding the wax injection process, the aim of the project is to achieve a better understanding of the key factors that will lead to better castings. The filling of the die during the injection has been studied. Some other phenomena such as shrinkage/warpage or creep under residual stresses are also studied, but not presented here. Two commercial investment casting waxes have been characterised in order to model their behaviour and predict mould filling and subsequent defects.This paper will present the models that have been used in our work, the simulation packages used, the experiments carried out to validate the modelling and exhibit the defects due to bad filling, and finally the numerical simulation results."

Jan 1, 2001

By Frank Field, Elsa Olivetti, Randolph Kirchain, Elisa Alonso, Gabrielle Gaustad

"The primary technological challenge to increased use of secondary raw materials is the presence of undesirable elemental species in scrap streams. Recent literature indicates that this may become exacerbated by accumulation of impurities over time. Devising strategies to mitigate this problem depends upon understanding the mechanisms of accumulation. This paper takes a first step at characterizing the extent of this issue by presenting a simple analytical model of recycling rate for materials experiencing exponential growth. Low potential recycling rates limit accumulation due to dilution. Empirical analysis of several major materials indicates that, even for current recovery rates, theoretical recycling rates can reach above 60%, making accumulation issues a possibility.IntroductionIt is well known that recycling of secondary materials can provide significant environmental and economic benefits. Energy savings, in particular, can be quite large when substituting secondary materials for primary. Nevertheless, over the past decade, the recycling rates within the U.S. of many materials appear to not be increasing as rapidly as one would predict or even at all (Figure 1). While many barriers exist to increasing materials recycling, one that is cited consistently by the literature and producers[1-3] is compositional limitations; that is the mismatch between the characteristics of secondary materials and those desired for the finished goods into which they would be transformed..One particular aspect of compositional limitations that is receiving increasing attention is the potential for progressive deterioration of the quality of secondary raw materials streams. For some materials, for example paper or polymers, this phenomenon is inherent and relatively rapid[4, 5]. As such, it is well documented and plays a significant role in recycling decision-making even for prompt or in-house material recycling. Conceptually, this issue can manifest in other secondary materials as well, albeit through a different mechanism.As materials are mixed, used, and reprocessed during recycling, they come into contact with and often pick up other elements. The presence of these, so-called, tramp elements alters the original known composition, possibly requiring additional measurement and processing and may even preclude economic, productive reuse; ultimately, this unintentional pick up is unwanted. A growing number of studies and literature would suggest that accumulation of unwanted elements is an emerging problem, in most recycled material streams. Table I provides a brief literature review of various recycled material streams and the accumulated elements noted as problematic by various authors"

Jan 1, 2008

By D. M. Hausen

Multiple drill sections through many of the numerous breccia pipes in the American Eagle copper deposit at Copper Creek, Arizona, have been evaluated by means of alteration and geochemical data. Contoured plots indicate vertically plunging, concentric, cylindrical shells of alteration and mineralized rock that are similar in structure, geometry, magnitude and petrology to the San Manuel-Kalamazoo Deposit, located about 14 miles to the southwest. Both deposits are similar in dimension and consist of multiple, irregular, rod-shaped injections of porphyry into a granodiorite host. Analogous to the San Manuel-Kalamazoo Deposit, most of the porphyry plugs are oriented parallel to the cylindrical axis of the "ore shell". A continuously mineralized, elliptical shell, inferred from deep drilling, is capped by a flatter zone of copper mineralization. Above this flat zone, copper-bearing fluids were channeled upward along conduits that correspond with quartz-sericite "breccia pipes". At depth, zones of sericite and K-feldspar alteration products exhibit conformable relationships with the copper deposition. A "bullet-shaped" ore shell, with a nearly vertical axis, is proposed to explain the conformable zones of altered and mineralized rock. The "nose" or top of the "bullet" is 1800 to 2300 feet below the surface, and structurally controlled in part by steeply dipping Hi and ENE faults. If correct, this model suggests that the vertical ore shell may extend to great depth.

Jan 1, 1988

By R. Padilla

In most of the Chilean copper and gold concentrates, arsenic is present mainly as enargite, Cu3AsS4, which at the conventional roasting or smelting temperatures decomposes liberating arsenic as gaseous compounds. The objective of this investigation was to study the decomposition reaction of enargite in an inert atmosphere in the range of 500 °C - 750°C. The results obtained indicated that the decomposition begins at about 525 °C. Two distinct regions in the temperature dependence of the decomposition rate were observed: a low temperature region between 525 °C to 650°C and a high temperature region between 650 °C to 725 °C. The X-ray diffraction analysis suggests that the decomposition of enargite occurs through the formation of intermediate tenantite, according to the following sequential reactions: 4Cu3AsS4(s) ? Cu12 As4S13(s)+ 3/2S2(g) Cu12 AS4S13(s) ? 6Cu2S(s) + 2As2S3(g) + 1/2S2(g) The decomposition kinetics was analyzed by using the model for a topochemical reaction of spherical particles: 1-(1-X) 1/3 = kt, which represented well the data. Apparent activation energies of 113 kJ/mol and 60.5 kJ/mol were found for the low and high temperature regions, respectively.

Jan 1, 1999

By Beatriz Amarai Campos, Jorge Alberto Soares Tenorio1, Denise Crocce Romano Espinosa, Adriana Johanny Murcia Santanilla

"The aim of the present work is to investigate the recovery of nickel from obsolete cell phones printed circuit boards. The printed circuit boards were firstly submitted to a grinding process and then leached in sulfuric acid. Nickel was extracted from aqueous solution using Cyanex 272. Aqueous/organic ratio was 1/1. The effect of both pH and modifier addition on selectivity of extraction was investigated.IntroductionCurrently, electric and electronic equipments (EEE) have become a necessity to the modern life. Associated with this necessity comes the continuous and increasing replacement of those equipments by new ones. The accelerated technology advances are responsible for the generation of electric and electronic waste. This waste can be dangerous not only to human health but also to the environment. Waste of electric and electronic equipments (WEEE) has a variety of components and metals in its composition becoming a potential pollutant to the environment when not properly discarded. Its wrong disposal causes a loss of materials that could be recovered and reused. Therefore WEEE treatment is an important matter because it can assist the reduction of waste generated and the recovery of valuable metals.Printed circuit board (PCBs) is an essential component of EEE and is typically very complex from a chemical point of view. Several metals may be present in its composition, such as cooper, nickel, iron, zinc, lead, tin and silver1''. This characteristic hinders the development of a simple treatment, making it necessary the application of chemical and mechanical processing for their recycling'4'. The UN estimates that approximately 20 to 50 million of tonnes of WEEE are generated worldwide each year."

Jan 1, 2011

By Milton Manrique, Edgar E. Vidal, Patrick R. Taylor

"Ultrafine zirconium carbide powder has been synthesized using zircon concentrate and methane in a thermal plasma reactor. The effect of several experimental variables, such as power used and zircon particle size, on the conversion has been studied. A thermodynamic analysis of the possible reactions and stable compounds was performed. A mathematical model that describes the in-flight decomposition of zircon particles was developed based on a description of the temperature and velocity profiles calculated in the reactor. It was shown that the formation of zirconium carbide from zircon and methane is thermodynamically possible. Complete 'vaporization of zircon in the reactor is predicted when the particle size is below 45flm and the effective power entering the reactor is 15 kW. The powders were collected and characterized by XRD, SEM, TEM and chemical analysis using ICP. Results of the product analysis indicated the presence of zirconium carbide, zirconium oxide, silicon carbide and silicon oxide.IntroductionIn recent years there has been an increased interest in the production of nanometric sized powders of ceramic materials for use in advanced materials applications. One possible method to produce these powders is with a thermal plasma reactor, which offers high temperatures and fast quenching rates. This technology has been called - Thermal Plasma Synthesis - [1].Zirconium Carbide (ZrCx) has typical properties of transition metal carbides: elevated hardness - between alumina and diamond - a high melting temperature of 3420°C and high chemical stability at room temperature [2]. ZrCx has a Bl crystal structure with deficiencies in the number of carbon atoms in the cell with x between 0.6 and 1 [3]. Different methods have been used to produce ZrC, one method is by direct reaction of zirconium hydride or halide with carbon. Other methods used are direct reduction and carburization of zirconium oxide (Zr02) and reaction of metallic zirconium with a caburizing gas such as acetylene [3]. Recently small films of ZrC have been obtained using a sputtering device [4,5]. ZrC has been used in nuclear plants as a low neutron absorbing and high mechanical resistant refractory material and also as a constituent in cathodes made of UC-ZrC [6]. It is also used in the form of tubes, boats and crucibles to handle molten metals and as part of electronic devices used for thermoionic transducers. Recently ZrC has been used along with zirconium diboride (ZrB2) to produce composite materials [7,8]."

Jan 1, 1996

By Hideki Yarnarnoto

The simultaneous removal for NH4+ and PO43- in aqueous solution was carried out by using Ca type zeolite synthesized from coal fly ash. The effect of pH on the cation exchange capacity and adsorption properties of the obtained zeolite, the simultaneous removal of NH4' and ~04'. in various solutions and the mechanism of simultaneous removal were investigated respectivel? ,The Ca type zeolite used in this study can simultaneously remove NH4+ and PO43- In aqueous solution without releasing counter ion, and this method gives great advantage over the other ordinary removal methods.

Jan 1, 2002

By Min Chen, Cui-huan Huang, Zhen Tian, Jian-hong Dong

"The present work studied the production of Fe-Si-Mn alloy from adjusted converter slag by thermodynamic analysis. The results showed that solubility of SiO2 in the molten slag increased with increment of temperature, and it is about 80% at 1800 ?. With increment of SiO2 content, a(MnO) and a(CaO) decreased, and a(FeO) increased to the maximum when w(SiO2) is about 30%. As a result, the reduction of the slag was in the order of Fe?Mn?P before SiO2 reduction, the reduction order was Fe?P?Mn?Si when SiO2 content in the slag was from 46.4% to 54.2%, and changed to Fe?Si?P?Mn when SiO2 content exceeded 54.2%. The mass fraction of Si in the alloy phase increases with increasing of w(SiO2) in the slag, and the mass fraction of Si in the alloy reached to 62.2% at 1800 ?.IntroductionFerroalloy production is a high energy consumption and high pollution industry[1-2]. If ferroalloy production could be produced from molten slag by addition of carbon-reducing agent, the valuable metal and oxide in the slag can be recycled, most importantly, if the high-temperature resource carried by molten slag can be made full use in the field of ferroalloy production, the power consumption of ferroalloy production could be cut down greatly.Converter steel slag is a kind of byproduct in steelmaking processing increasing rapidly with the increment of crude steel, but the utilization ratio is low. Most heat recovery research is still in the experimental stage except the heat recovery of blast furnace slag by water quenching method, at present[3-4]. It is of great significance for enterprises to energy saving and emission reduction if the molten steel slag could be utilized directly. Not only the reuse methods of liquid steel slag material can be promoted, but also the use of heat carried in the slag could be achieved. The basicity of converter slag is high and the activity of SiO2 is low so the reduction of SiO2 in the slag is little. The compositions of slag and metal phases were calculated by Factsage program on different conditions to explore the reduction of converter slag for recovery of valuable metals and an efficient new way to use the high-temperature heat combining with the current reuse and research status of converter slag. Further, the improvement of components activity in slag and the increase of Si concentration in the metal were also dicussed."

Jan 1, 2012

By B. Fresz

Before aluminum is utilized in automotive bodies, the longevity of the electrodes employed in the resistance spot welding of aluminum must increase. This paper explores the affects of electrode composition on electrode life. To compare these variables, electrode tests were completed on a Taylor Wield welding machine using, Cu-Cr, Cu- Zr, Cu-Cr-Zr, Cu-Be, and Glidcop electrodes tested to 12.5%, 25%, 50%, 100%, and 150% lifetimes. Electrode diameters were found via a magnification technique using a PULNIM video camera attached to a low magnification Wild Heerbrugg stereo-zoom microscope. From these measurements, graphs of electrode life verses face diameter and weld number verses face diameter were created. Analyses of these graphs suggest that a single failure mechanism is responsible for electrode failure, though the number of welds until failure (100% electrode life) varied with composition (700-2000 welds).

Jan 1, 1999

By Qian Li, Haiyan Leng, Kuo-Chih Chou, Haoyuan Xiao, Zhigang Yu

Magnesium borohydride and Magnesium alanate were synthesized by mechanochemical metathesis reaction. The thermal decomposition behaviors of Mg(BH4)2-nMg(AlH4)2(n=0.5,1) systems were investigated as potential hydrogen storage materials. The results showed that the systems started to desorb H2 at 120 ℃ and desorbed 3.9 wt. and 4.9 wt.% H2 below 300 ℃ when n equals 0.5 and 1, respectively, while individual Mg(BH4)2 started to desorb H2 at 250 ℃ and desorbed only 0.82 wt.% H2. Because of the exist of the Mg(AlH4)2, the isothermal desorption kinetics of Mg(BH4)2 in the Mg(BH4)2-0.5Mg(AlH4)2 systems was 50% faster than that of pristine Mg(BH4)2. In addition, the re-hydrogenation rates also increased 49.4% and 37.9%.

Jan 1, 2015

By Toshitaka Ota, Hisao Suzuki, Minoru Takahashi

"Perovskite-type lead zinc niobate (PZN) exhibits excellent electrical properties such as high dielectric constant, high electrostrictive coefficient and superior piezoelectricity. Therefore, PZN ceramics are very promising for high performance electronic devices. However, perovskite phase PZN is not stable under the ambient atmosphere. Accordingly, it is very difficult to prepare single-phase perovskite PZN ceramics. In this study, A-site cation of lead was partially substituted for barium to stabilize the perovskite phase of the PZN (Ba-doped PZN) powder. In addition, molecular design of an alkoxide precursor was controlled for a low-temperature processing. As a result, molecular design to suppress the lead-volatilization during calcination was preferred for a low-temperature processing. Processing temperature for a single-phase perovskite was depended on the amount of barium dopant. Doping of20 mole% of barium resulted in the single phase perovskite at 900 °C. The temperature for the single phase perovskite of Ba-doped PZN powder, which depended upon the amount of Ba-doping, was lower than that of the powder prepared by the atmosphere controlled conventional powder processing at least by 150 °C.IntroductionFerroelectric thin films and powders with perovskite structure are of renewed interest for micro-electronic applications, including ferroelectric random access memory (FRAM), dynamic random access memory (DRAM), and thin-layer capacitors integrated onto a silicon wafer [1-3]. In addition, recent advancement in micro-machine requires a high performance micro-actuator [4]. A perovskite type relaxor of Pb(Zn113 Nb213)03 is one of the promising materials for a high performance capacitor and microactuator because of their high permittivity and electrostrictive coefficient [5]. Therefore, this paper focuses on the low temperature processing of Ba-doped PZN powders.Chemical solution deposition (CSD) from molecular-designed alkoxide precursor solution is one of the most promising techniques for processing high-performance powders and thin films because it offers precise control of compositions on a molecular scale as well as a low processing temperature [6]. However, chemical solution deposition of perovskite type PZN powders and ceramics are very difficult because of the formation of stable pyrochlore phases. Therefore in the past, PZN powders and single crystal have been prepared by the hydrothermal method or flux method as well as the partial substitution method of a A-site cation [7-10]. In this study, a suitable molecular design for a preparation of perovskite type Ba-doped PZN powders with a chemical solution deposition process is investigated as well as the effect of A-site cation substitution. Chemical solution deposition from molecular-designed alkoxide precursor solution is expected to decrease the amount of a A-site substitution and/or a crystallization temperature for a single phase perovskite. This paper describes ""the relation between molecular-design and processing temperatures for a single-phase perovskite of Ba-doped PZN powders in comparison with the conventional oxides mixing method."

Jan 1, 2000

By Jianhui Wu, Jing Zhan, Chuanfu Zhang, Zhijian Wang, Chu-ping Xia

"A novel technology about interactive roast of complex bismuth sulfide ore with low grade and Pyrolusite was put forward using the low-grade bismuth sulfide ore and pyrolusite as raw materials. The predominance diagram of Bi-Mn-S-O system was drawn by thermodynamic calculations. Stable coexistence area ofBizO3 and MnSO4 and its control condition was obtained. The interactive roast conditions including roasting temperature, roasting time, the ratio of n(MnO2)/n(S), ventilation rate and so on are investigated systematically. The results show that the sulfur-retained ratio reaches about 98%, in which formation rate of MnSO4 was 94.04%, most of the residual sulfur in the ore exist in the form of BhsO32(SO4)10 in the roasting products The optimum roasting conditions were as follows: roasting temperature of 650°C, roasting time of2h, 1.4 for n(MnO2)/n(S) and 140L/h for ventilation rate.IntroductionBismuth is a ""green"" rare metal with the characteristics of safe, nontoxic and low melting point[l].The use of bismuth and its oxides is extending from traditional fields such as pigment, fusible alloy, bismuth class of drugs and metallurgical additives to the high-tech fields such as semiconductor, high-temperature superconducting materials and nuclear power and so on. Bismuth is one of the precious advantageous resources in China which owns the most abundant bismuth resources in the world. Bismuth metallurgical process is divided into the pyrometallurgy and hydrometallurgy [2-4]. Hydrometallurgy for bismuth is mainly used for the processing oflow-grade complex bismuth ore, whose key steps are oxidative leaching process of the bismuth sulfide ore by strong oxidants(FeCb, Clz, HNO2 etc) in hydrochloric acid system. Therefore, the corrosion of strong oxidants, high demand for equipments and poor operating environment are its inherent disadvantages. Pyrometallurgy for bismuth is mainly used for the processing of high-grade bismuth raw materials or concentrate, which is the main method for bismuth metallurgy at present."

Jan 1, 2013

The physico-chemical principles of chloride hydrometallurgy are reviewed to rationalise the complex chemistry in chloride-based processes for metal sulphides in terms of the predicted Eh-log[Cl-] relationships, measured changes in activity of H+, Mz+, Cl- and solubility of Ag(I), Cu(I), Cu(II), Pb(II), Ni(II), Au(III), Sb(III) and Bi(III). These changes reflect the nature of chemical speciation, competing effect of hydration/hydrolysis and chloro-complexation,composite effect of increasing acid and/or salt concentration and decreasing water activity. Rate data for the dissolution of PbS and ZnS in HCl containing Fe(III) or Cu(II) are compared and contrasted to highlight the effect of acid and chloride concentration, water activity, and the nature of oxidant. It is shown that LiCl, NaCl and HCl influence the kinetics of oxidative PbS leaching based on their effect on solubility of PbCl2 co-precipitated with elemental sulphur on the mineral surface. Evidence for the beneficial effect of Cu(II) in sulphide leaching is discussed.

Jan 1, 2003

By M. A. Rabah, F. E. Farghaly, M. A. Motaleb

"Wastewater from industrial galvanization industry was reclaimed under current flow stream conditions. Results showed that the raw water contains 0.7 % by weight total suspended solids (TSS) causing turbidity amounting to 30. Measurements of Zeta potential as a function of pH revealed that solid separation takes place at pH 9. Addition of H2O2 to the polmer solution helps to oxdize ions of iron and zinc metals toinsoluble ferric oxide and zinc hydroxide to a higher state of oxidation. Addition of 5 mg/L of cationic magna flocculants polymeric solution helps the rapid separation of the turbidity. Separation of floccules so formed takes place by filtration. Addition of peroxide ions to the turbid wastewater confirms the physical stability of the flocs so formed. Impurity flocculation takes place in few seconds. Maximum temperature for safe solid removal was <30°C. The treated water was pure and safe for recycling or use in domestic purposes.IntroductionStocks and et. al. [1] show that the galvanizing process introduces spent pickling acid waste production, but its major constituent, could be used. Survey of the operational procedures adopted and the acid wastes produced by UK Galvanizers are reported. Various methods to recovery spent acid of suitable composition and to eliminate zinc contamination was considered. Application of the Kleingarn acid management system reduces waste volume, saves hydrochloric acid (HCl) and increases component throughput whilst, in conjunction with zinc elimination, could allow recycling of the majority of galvanizer’s acid wastes.Dahab [2]; Kerney [3] reported recycling of galvanizing products, including pickleliquor. Kerney suggested a mobile treatment plant for recycling pickling acids. Dahab found that pollution reduction could be achieved by relatively simple operational changes to the process that gave fairly short payback times.Rozenblat and et. al.[4] studied the extraction of zinc (II), iron(III) and iron(II) with Tributyl phosphate (TBP) from hydrochloric acid solutions containing high zinc(II) concentration. Two technological approaches for the separation are considered. Firstly, the selective extraction of iron(III) (iron(II) is oxidized to iron(III)) over zinc(II) with TBP deficiency. Secondly, iron(III) reduction to iron(II) followed by zinc(II) selective extraction with an excess of TBP. Prior stripping, the organic phase was washed with small amounts of water. Scrubbing of TBP solutions containing iron(III) contaminated with zinc(II) gives always a mixture of zinc(II) and iron(III) which must be recycled to the extraction step in continuous process. The following technological concept is proposed: reduction of iron(III) to iron(II), extraction of zinc(II) with 5-10 volume excess of TBP, washing of TBP phase contaminated with iron(II) with small volumes of water and recycling of the scrubbings and stripping of zinc with water."

Jan 1, 2008