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By P. Maraboutis

Iron removal by precipitation as jarosite from Fe-Ni-Co sulfate solutions, (synthetic or real, resulting from laterites leaching) has been investigated. Precipitation was carried out at 95 C, and at an initial pH 1.6, which was either kept constant with CaCO3 or Li2CO3 additions, or left to drift with the evolution of the reaction to lower values. The precipitation of K-, NH4- and Na- jarosite was initially examined using synthetic solutions. In all cases, hydronium ions were incorporated into the precipitate as well. Residual iron in solution was lower (0.2-1 g/1) and equilibrium was achieved faster (within 4-8 h) when precipitating K¬jarosite at constant pH, using CaCO3 for neutralization. Nickel and cobalt losses were small. Na- jarosite precipitation was also studied from real solutions with high initial iron content, under constant pH=1.5, controlled with CaCO3 additions, and it was shown that low residual iron concentration in solution (0.3-0.5 g/1) can be achieved again, with relatively small nickel and cobalt losses. The thickening and filtration characteristics of the precipitates were excellent in all cases examined.

Jan 1, 1988

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 C. A. Morais

The present work describes the development of an efficient and relatively simple process to obtain high grade CeO2 from a mixed rare earth chloride solution. The process involves cerium oxidation and precipitation by addition of a KMnO4-NaCO3 solution. The experiments were carried out at room temperature (25 1° C). The results indicated that the major parameters affecting cerium recovery are the molar ratio of KMnO4/Ce, the initial acidity of the chloride feed solution and final pH of Ce(OH)4 precipitation. In strong acid solutions (pH < 1), the oxidation of Cl to Clo took place in addition to the oxidation of Ce(III) to Ce(IV), so increasing the permanganate consumption. Conversely, low acidity (pH >3) led to coprecipitation of the other rare earth elements. Under the selected conditions, cerium was selectively precipitated as ceric hydroxide, together with some manganese dioxide. Further purification was carried out by the dissolution of Ce(OH)4 in HCl, followed by precipitation as cerium carbonate. The filtrate was neutralised with a Na2CO3 solution in order to recover the associated rare earth elements for further separation. The final product, assaying 99.7 % CeO2, was obtained with a recovery of nearly 100%.

Jan 1, 2003

By Mikiya Tanaka, Mikio Kobayashi, Mansour A. S. A1Ghamdi, Kenji Tatsumi, Yukinori Saiki, Hirotaka Senba

"In order to recover nickel ion in a spent electroless nickel - phosphorus alloy plating bath and, at the same time, to remove impurities such as iron and zinc, the applicability of solvent extraction with LlX84I as the extractant has been investigated using actual spent solution. Although the extraction efficiency of nickel from the spent solution is considerably lower than that from the nickel sulfate-nitrate solution, nickel in the spent solution is selectively extracted with high efficiency at the pH of 6 - 7. The extracted nickel is effectively stripped by sulfuric acid at a pH of less .than· 3. On the basis of these results, a· flowsheet for recovering nickel from the spent solution is proposed Chemical equilibrium calculations of the spent solution has shown that the complex formations of nickel with anions such as lactate and phosphonate ions become predominant in the pH range between 2 and 6. This results in the depression of nickel extraction efficiency from the spent solution as compared with that from the .nickel sulfate-nitrate solution. By combining these aqueous equilibrium calculations with the· extraction model considering the extraction stoichiometry and the aggregation of the extractant in the organic phase, the extraction behavior of nickel is quantitatively predicted.IntroductionElectroless plating is indispensable for the recent advanced industries such as the electronic and mechanical industries. Electroless plating baths are repeatedly used by supplying the metal salts; however, the accumulation of the counter anions of the metal ions, the components formed by the oxidation of the reducing reagents in the plating baths, and the metal ions as impurities dissolved from the surface of the objective materials degrades the· quality of the plating. Thus, the baths are finally treated by a precipitation method to form a large amount of metal sludge, which is disposed in dumping sites. Therefore, from the standpoints of environmental protection and resource preservation, it is highly desired to establish a recycling process of the plating baths with minimum emission. Solvent extraction seems to be one of the 'suitable methods to recover metals from the spent electroless plating baths, because the concentration of the metal ion in the baths is relatively high, which is advantageous to solvent extraction as compared with the ion-exchange and adsorption methods. Some studies about the application of solvent extraction have already been carried out using simulated spe11t electroless plating baths [1-3]."

Jan 1, 2000

By B. Manana

In heap leaching, the oxidative dissolution of value minerals encapsulated deep within large particles cannot be fully understood on the basis of the bulk solution conditions relative to variable solution conditions near the mineral surface. In the present study, the diffusion of the oxidising species through inner particle pores is simulated in a model apparatus that separates an inert platinum electrode under controlled reduction potential from the bulk solution through narrow pores of varying length. The Cu-NH3 system was selected as a model system and Cu(II)/Cu (I) as the redox couple of interest. Platinum probes inserted in the pores allowed the measurement of varying redox potentials along the pore length. Results showed that in a 10 mm pore, there exists a narrow (0.5 mm) zone near the reduction surface that is depleted of the oxidant and in which its supply is strongly diffusion limited, even if it is in abundance in the bulk solution. The consistent presence of this narrow diffusion region across all experimental results indicated that the transportation of the reduced species away from the reaction surface had the most significant influence on the potential variations within the pore. This was further supported by the minimal effect of varying concentrations of both Cu(II) and dissolved oxygen on the solution potential within this region.

By Joseph C. Milbourne

Tetra Technologies CCIX? (continuous countercurrent ion exchange) system has been involved in a wide range of uranium concentration, separation and purification applications over the past 40 years. Uranium ion exchange applications have ranged from the treatment of copper heap leach solution containing 5 parts per million of uranium to the treatment of high strength sulfuric acid solutions containing several thousand parts per million of uranium. The flexibility and the countercurrent mode of operation and other unique features of the CCIX? have resulted in successful uranium recovery from these solutions and many others.

Jan 1, 1995

By K. Morsi

Carbon nanotube (CNT) reinforced metallic composites have been recently generating significant scientific interest, due to their expected superior properties compared with other composites. Out of the metallic matrices investigated for reinforcement with CNTs, aluminum has received considerable attention. A major problem has been the dispersion of CNTs in metallic matrices. This paper discusses preliminary results on the mechanical dispersion of CNTs in aluminum powder, powder processing, stability and characterization of aluminum dispersed with CNTs at reinforcement levels equal to and below 5 wt.%.

Jan 1, 2009

By Yuanbo Zhang, Guanghui Li, Zhenyu Fan, Tao Jiang, Xiaohui Fan

"Iron ore sintering process is the main source of SO2 generated in the steel industry, of which the discharge amount of SO2 emission accounts for about 60% of the total. Aiming at the features of sintering flue gases and existing problems during the flue gas desulphurization, a technical route of flue gas circulation sintering (FGCS) for iron ores has been put forward. Under the simulated experimental conditions, effects of FGCS process on the main output and quality indexes and SO2 emission rule are researched using simulating flue gases. Compared the novel FGCS with conventional sintering process, SO2 in the final sintering flue gas is obviously enriched and the total exhaust gases can be reduced evidently. The decreasing of oxygen content in circulating gases has bad effect on the sintering indexes. Increasing the oxygen potential is beneficial to obtain high quality sinters. This investigation shows that the FGCS process is promising.IntroductionSteel is a kind of essential material for modern society, but steel-making process is characterized by high energy-consumption and emission as well as heavy environmental pollution. Chinese steel industry has developed rapidly in the last decade, and the environmental problem caused by ironmaking and steelmaking have also aroused the greatest concern, especially the atmospheric pollution caused by SO2, CO2, etc. Iron ore sintering process is the main source of SO2 generated in the steel industry, of which the discharge amount of SO2 emission accounts for about 60 % of the total. The development of the desulfurization process for sintering flue gases to reduce SO2 emission in sintering process is not only the requirements of sustainable development but also the most important environmental tasks for steel industry [1-5]."

Jan 1, 2011

By A. V. Tarasov

In order to improve technical, economic and environmental performance of hydrometallurgical processing of intermediate products containing copper and nickel, the Gintsvetmet Institute and the IMET Institute of the Russian Academy of Sciences have conducted studies into the efficiency of the use of alternating current of industrial frequency on processes applied for hydrochemical leaching of various copper- and nickel-containing materials. It has been found that: 1.Imposition of alternating current over the process of leaching of softly reduced nickel oxide with recycled copper sulfate solutions resulted in an increase by 20 to 30% of the rate of the copper cementation process and reduced by 20% its activation energy. At the same time, the recoveries of nickel, cobalt and iron to the leach solution increased up to 82.2%, 78.5% and 57.1%, respectively, and that of copper to the cement precipitate up to 74%. Optimal process conditions have been identified with respect to the current density, electrode material, copper concentration in solutions and the process temperature. 2.In the process of hydroelectrochemical sulfuric acid leaching of nickel and copper sulfides, the grain size, the phase form of sulfides, the solution composition (H2SO4, Cl?, Cu2+, Fe3+)and the current amperage had an effect on the nickel recovery to the solution, which reached 90%, while the degree of copper transfer to solution did not exceed 20%. The process of hydroelectrochemical sulfuric acid leaching of nickel and copper sulfides with an addition of Cl? made it possible to selectively recover nickel into the leach solution along with concentrating copper in the leach residue. 3.When subjecting samples of commercial-grade magnetic fractions of converter matte to sulfuric acid leaching, the imposition of electric current, the concentrations of sulfuric acid and chloride ion in the solution and the duration of the reaction process had an effect on the process. The nickel recovery was 85% and that of cobalt and iron was 95% and the recoveries reached 97.5%, 98.3% and 99.8% as a result of repeated treatment of the primary residue under similar process conditions. Up to 75% of copper, 75% of sulfur and 99.0-99.5% of palladium was concentrated in the solid reach residues. The experimental data obtained indicates that the use of AC for hydroelectrochemical sulfuric acid leaching for separation of copper- and nickel-containing intermediate products has favorable prospects.

Jan 1, 2003

By Bowen Li

Silicon Carbide is an excellent refractory material. Its physical properties make it extremely useful, particularly in applications where corrosion resistance and wear are important considerations. Commercial silicon carbide refractory is frequently manufactured by bonding silicon carbide particles with clay; however, clay may cause problems in the sintered products. This study investigates the potential of replacing a portion of the clay with andalusite powder. The results show that micron size andalusite powder can improve not only the strength of the refractory but also the sinterability. The mechanisms for these improvements are discussed.

Jan 1, 2006

By A. S. Mustafinova, A. A. Zharmenov

"Production of electrolytic copper is characterized by large volumes of acidic spent solutions the utilization of which requires considerable expenditures of neutralizing agents. At present, an economically substantiated technology does not exist for treatment of sulfuric acid rinse solutions and spent copper electrolyte which will allow for repeated use of the acid and the metal salts. Therefore, for this aim the most advantageous is the use of electromembrane methods. In the paper there is stated the essence of developed technologies which are distinguished by low waste and provide the extraction from the solutions of metallic copper, nickel and sulphuric acid. There are also considered methods of copper electrolyte processing allowing to regulate its composition by that or another component (H2S04, Cu, Ni, As).On the base of the detailed study of the behaviour of various types of ion- exchanger membranes in copper-, nickel-, zinc-, arsenic- bearing sulphate solutions there is realized the selection of the most suitable membranes (MK -401, MA-411, MB-2 and MKL-l/MAL-2).Some variants of electro membrane processing of spent solutions of the hydrometallurgy process have passed productions tests on a number of copper-electrolyte enterprises of the countries of CIS (cooperation of Independent States). These tests showed high efficiency of developed methods."

Jan 1, 1997

By Yasuhiro Konishi, Yoshiyuki Noda

"This paper describes a new processing of rare-earth oxide precursor, in which rare-earth carbonate powders are precipitated directly from emulsions of rare-earth loaded carboxylate solutions, using CO2 gas and water. This synthetic route of rare earth carbonate is a combined process of the stripping and precipitation stages in a conventional solvent extraction. Using this technique, lanthanum carbonate and yttrium carbonate were prepared at temperatures of 10 to 80°C and CO2 pressures of 0.1 to 3.0 MPa for 120 min. The rates of carbonate precipitation in a batch autoclave were sensitive to processing parameters such as CO2 pressure, temperature, and organic-phase composition. The particle size distributions of the carbonate powders were markedly dependent on temperature and C02 pressure.IntroductionSolvent extraction is the most appropriate commercial technology for separation and purification of rare earths. In typical commercial processes, the rare earths are stripped from loaded solvent extractants using aqueous solutions of mineral acid. After adjusting the pH of the aqueous strip solution, the rare earths are precipitated as insoluble powders of oxalates or carbonates, from which oxides can be produced by calcination. Such conventional processing can be simplified when the stripping and precipitation stages are combined by emulsifying rare-earth loaded solvent extractant with aqueous oxalic acid solution. It is likely that the single-stage precipitation stripping results in a marked decline in the consumed amounts of precipitating and neutralizing agents, thereby saving on both running and capital costs.Yoon and Doyle1) first demonstrated that oxalate powders of lanthanum and yttrium are directly precipitated from rare-earth loaded carboxylic acid solvent extractant when contacted with aqueous oxalic acid solution at ambient temperature and atmospheric pressure. Yttrium oxalate pow4ers were also prepared by precipitation stripping of di-(2 ethylhexyl) phosphoric acid. (D2EHPA) extractant using oxalic acid-hydrochloric acid solutions. 2) Moreover, neodymium oxalates were directly precipitated from organic solutions of tertiary aliphatic monocarboxylic acid and 2-ethylhexyl phosphonic acid mono-2- ethylhexyl ester using aqueous oxalic acid solutions, and powder characteristics of the resulting oxalates were compared with those of powders by the conventional solvent extraction routes. 3 • 4) Recently, attention has been directed towards the influence of processing parameters on the particle size distributions of yttrium oxalate precipitates. 5)"

Jan 1, 2000

By K:-I. Rhee

The recovery of tellurium from Te-cement obtained during the processing of copper anode slimes was carried out by a series of hydrometallurgical processes, i.e. leaching Te-cement in NaOH solution, precipitation of impurites with the addition of Na2S followed by direct electrowinning of tellurium in NaOH solution. The optimum conditions for each process were determined and discussed in terms of various parameters associated with each step to maximize the recovery and purity of tellurium. The final purity of tellurium from electrowinning in alkaline solution was found to be more than 99.9 %.

Jan 1, 1997

By Rui Mao, Ke-Xin Nao, Jian-Liang Zhang, Xiang-Nan Xu, Meng-Fang Wei

"In this research, fundamental characteristics of dust and sludge containing iron from the dusting system of sintering process, blast furnace, oxygen converter and rolling process in steel enterprise were studied by chemical analysis, X-ray diffraction analysis, optical microscope analysis, scanning electron microscopy analysis, particle size analysis and other analysis means. Development direction of resource utilization for dust and sludge containing iron from steel enterprise was put forward on the basis of above study.IntroductionDust and sludge containing iron for steel enterprise mainly come from the dusting system of sintering process, pelletizing process, blast furnace, oxygen converter, rolling process and other related process. Iron content of dust and sludge is between 30% and 70%, and they also contain certain content of carbon, calcium oxide, magnesium oxide and harmful elements [1-3]. Output of dust and sludge is determined by raw materials conditions, technological processes, equipment configuration and management level. Dust output in sintering process accounts for about 2% to 3% of the sinter production, while dust and sludge from iron making and steel making process respectively take up 3% to 4% of hot metal and crude steel production, and the solid waste from rolling process accounts for about 0.8% to 1.5% of the output of rolled products [4,5]. Dust and sludge contains Fe, CaO, MgO, C and other valuable resources, it will not only result in the waste of resources, but also cause serious pollution to environment ifthe dust and sludge are not recycled. China's crude steel production in 2012 is about 700 million tons and output of dust and sludge containing iron is nearly 60 million tons, so, it is of great significance to have a resource recycling for dust and sludge containing iron from steel enterprise."

Jan 1, 2014

By Guillermo J. Román

The precipitation of copper and zinc as cements from a copper alloys&apos; spent pickling solution has been studied at laboratory and pilot scale, with the objective of designing an economic process to recover both metals and render a solution to be either recycled to the pickling process or treated in a standard fashion and produce a non-hazardous sludge. The sulfuric acid spent pickling solution already containing copper and zinc was used first to dissolve another solid residue originated in the copper alloys foundry to neutralize part of the acidity. The resulting enriched solution was treated separately with two reductants,; sodium borohydride and iron powder varying pH and excess of reductant under constant agitation. Under the best conditions, precipitation of over 95 percent of zinc and copper was achieved together with the reduction of lead and cadmium contents respectively. A process for the combined residues treatment is proposed.

Jan 1, 1995

By H. K. Lin

Thermodynamics of Cu-C1-H2O system and the kinetics of copper dissolution in cupric chloride solution were studied with emphasis on possible difficulties which may occur during copper electrowinning. E,-pC1 diagram of this system wasestablished. Equilibriumdistributionof various copper chloride complexes of different valent states at the presence of metallic copper was computed through the relations of the simultaneous equilibria. The mechanism-of copper dissolution in the cupric chloride solutions was proposed and the mechanism of copper electroposition was discussed. The researched results were used for guiding the investigation of copper electrowinning from cupric chloride solution.

Jan 1, 1991

By T. Goda, H. Kiuchi, M. Iguchi

"IntroductionThe utilization of silver in the electronic industry has been increasing in recent years. It is desirable that valuable metals are recovered from the used scraps of these industrial goods. Condensor chips, for example, contain silver, palladium, and Ag-Pd alloy. The dissolution behavior of silver was studied assuming that scraps such as used condensor chips in which Ag-Pd paste is used are subjected to wet treatment.ExperimentalIn this study the powder, granules, and flakes of silver were used in these nitric acid leaching experiments. The nitric acid solution was agitated in a glass reactor with a magnetic stirrer and heated to the required temperature. The experiment was started by putting the silver sample in the solution. After the leaching, the solution was filtered and the concentration of silver in the filtrate was analyzed by ICP.ResultsIn dilute nitric acid of less than 5 N, silver powder dissolved easily with increase in the concentration of nitric acid and temperature. However, the more intensive the stirring of the solution was, the lower the dissolution quantity became. Fig. 1"

Jan 1, 2000

By R. F. Hammen

Copper is one of the most widely used metals in industrial processes and is also present in most mining operations. Extraction of copper from solutions often proves difficult due to the presence of complexing agents. ChromatoChem, Inc. has developed a Solid Phase Extraction (SPE) support (HiPAC) for removal and recovery of metals from wastewater. The HiPAC SPE support employs chelating agents covalently coupled to a long linker molecule. Several solutions containing copper and complexing agents were tested including 1) copper and carbonate, pH 9.8, 2) mixed metals and anions with copper and cyanide, pH 11, and 3) copper and the chelating agent EDTA, pH 11. The copper was extracted from solutions one and two at high pH, but the EDTA containing solution needed the pH lowered to make the copper available for capture. In each example, the copper concentration was significantly reduced by HiPAC SPE treatment.

Jan 1, 1994

By V. G. Papangelakis

The implementation of a flow-through yttria-stabilized zirconia (YSZ) sensor for pH measurements in high temperature and concentrated electrolyte systems relevant to hydrometallurgical processing of nickeliferous laterites is discussed. Instrumentation involved the use of a custom made flow-through titanium electrochemical cell. Accuracy and validity of the pH measurements at temperatures up to 250C were assessed using concentrated sulphate process solutions ranging from synthetic binary sulphuric acid ? water solutions to progressively multicomponent metal ? sulphate solutions simulating laterite Pressure Acid Leach conditions. The measurements were also compared with theoretical models using recently obtained thermodynamic data. A difference of ±0.25 pH units was observed between measured and calculated pH values at temperatures. This is an acceptable difference given that these are the first direct high temperature pH measurements ever on the concentrated acidic sulphate solutions. This result is encouraging more research for the development of industrial electrochemical systems for direct pH measurements in autoclaves.

Jan 1, 2003

By Bohumír Cech, Jirí Hanika, Václav Veselý

"PET bottles are separated and subsequently crushed into flakes. Except for PET, these flakes contain PE, PVC, paper, adhesives, beverages remainders and mineral impurities. PET itself usually is a glycol and terephthalic and isophthalic acid polymer.The suggested method consists in PET flakes crystallization at 255°C. In the meantime, volatile substances evaporate and PVC disintegrates. Formed crystalline PET is crushed into small particles and then is subject to the basic hydrolysis at an atmospheric pressure. In addition to lye solution, glycol is added in the hydrolysis. Water is eliminated by boiling, which gives rise to suspension of sodium salt of terephthalic acid and glycol. The suspension is skimmed and the filtered glycol is vacuum distilled. Pure glycol is then the distillation product.Crystals are dissolved in water and the solution is filtered, which eliminates PE and impurities. Electrodialysis removes pure terephthalic acid salt from the solution. Glycol solution is returned to the hydrolysis. Terephthalic acid is precipitated by a mineral acid. Subsequently, it is washed and dried. The filtrate is separated through electrodialysis to lye and acid. The lye gets back to the hydrolysis and the acid is used for precipitation. Terephthalic acid and glycol are products in a “polymer grade” quality. The waste is a part of washing waters, distillation residues after glycol regeneration and a filter cake after the terephthalate solution filtration."

Jan 1, 2008