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By René Winand

Due to chemical and electrochemical behavior of the most common additives in copper electrorefining i.e. gelatine, thiourea and chloride ions, it is essential to simulate as far as possible true industrial practice while performing laboratory experiments. The three additives must be studied simultaneously, and added continuously to the electrorefining cell. Ratio electrolyte volume to cathode area; ratio bleed flow to cathode area; hydrodynamic conditions; residence time of electrolyte in the cell; current density; electrolyte and soluble anode must be as near as possible to industrial ones. Experiments performed in the author's laboratory show that under these conditions, reproducible results can be obtained at normal industrial current density and at high current density as well. Problems are however still encountered when developing a sensor for additives monitoring, due to electrolyte redox potential and to substrate influenced thin layer deposition.

Jan 1, 1995

By M. Omneya El-Hussaini, M. Galal Abdel Wahab, A. Mohamed Mahdy, M. Fathi El Shahat

"Um-Gheig Pb-Zn representative sample was collected from the main adite of Um-Gheig mine along Red Sea coast in Egypt. Its chemical analysis shows that, it contains 16% Zn, 2.3% Pb, 0.1% Cd and 0.1% B as elements of interest. After H2SO4 agitation leaching, the chemical composition of Um- Gheig Pb-Zn deposit ore residue assayed 2.26% Pb, 1.5% Zn, 0.085 % B and 0.01% Cd. This residue was leached with 20% HCl at S/L ratio 1/3 for 2 hours at 80o C. The chloride leach liquor was found to contain 18 g/l Pb, 13 g/l Zn, 0.1 g/l Cd and 0.75 g/l B with the corresponding leaching efficiencies 79%, 86%, 100% and 88% respectively. Lead was precipitated from the chloride leach liquor using concentrated H2SO4 to obtain PbSO4 with precipitation efficiency 96%. While boron was extracted by the selective resin Amberlite IRA743 with loading efficiency of 80%. On the other hand, Zn and Cd were precipitated using Na2S solution with 86.7% and 100% recovery efficiencies respectively.IntroductionLead-zinc ores occur in Egypt in a few localities distributed along the Red Sea coast between El Qusier and Ras Banas.. The reserve of the ore deposits has been estimated by Soviet and German Experts to be about 900,000 Ton, [1]. Onal et al., [2] recovered Pb from Pb–Zn sample containing 10.17 % Pb and 10.98 % Zn from Aladag in Turkey. El-Sherif, [3] used concentrated HCl to leach lead-zinc ore sample of Um-Sammuki area in Egypt. As had been published by Marchioretto et al. [4], the precipitation of heavy metals with lime, sulfide and caustic soda are the most commonly used economical methods for metal removal. Lead was completely removed from the anaerobically digested sludge by precipitation with NaOH and Na2S at waste water treatment plants. Mahdy et al., [5] had successfully extracted boron from the bittern solution of Qaron Lake by ion exchange resin (Amberlite IRA 743). The extraction of boron was mainly depending upon the pH value. They extracted 80% of boron at pH 5.5, while at pH 3.9 about 74% boron was extracted. Kabay et al. [6] used the column-mode to remove 1g/l of boron from geothermal waste water of the Kizildere-Geothermal Power Station by using Diaion CRB 02 Nglucamine- type chelating resins. In this regard, the removal of lead, cadmium and boron allow the residue to be reclassified as non hazardous material."

Jan 1, 2008

By Ozgul Dere Ozdemir, Muge Sari Yilmaz, Sabriye Piskin, Deren Sibel Kasap

"Galvanic sludge is generated at the end of the waste water treatment process of metal plating system. The waste sludge is one of the main hazardous solid wastes produced by metallurgical industries. It is caused the harm of human health and damage of the environment due to containing reasonable amounts of toxic metals (e.g., nickel, zinc, copper, chromium, iron, lead, cadmium, etc). The concentration of those toxic metals in the wastewater might reach 30% (w/w, dry weight) making their removal and recovery an interesting issue.In this study, synthesized titanium dioxide is used as adsorbent to remove nickel in leachate of galvanic sludge. The adsorption experiments were carried out isothermally at four different temperatures. The effects of pH, temperature, and contact time on nickel adsorption efficiency were investigated, and the optimum parameters were determined from the experimental studies. The experimental results indicated that pH, temperature, and contact time played a significant role on the adsorption capacity of nickel.IntroductionRapid industrialization has caused increasing the heavy metal concentration in biosphere with the industrial wastes. These wastes are generated in various industrial processes such as electroplating. Galvanic sludge is a hazardous waste that generates from metal plating industry by chemical precipitation of heavy metals from acidic or alkaline solutions during the waste water treatment process. Heavy metals are tend to bioaccumulate thus they are treated the living organism [1-2].Galvanic sludge is mainly disposed on landfills for these reason it is a big problem for environment. Galvanic sludge containing nickel (II) is common because nickel (II) is used in electroplating process [3]. In drinking water, nickel may cause health problems if found in amounts greater than the health standard set (MCLG: 0.1 mg/L) by the United States Environmental Protection Agency (EPA). The higher concentration of nickel (II) in ingested water may cause severe damage to lungs, kidneys, gastrointestinal distress, e.g., nausea, vomiting, diarrhea, pulmonary fibrosis, renal edema, and skin dermatitis [ 4]. For these reasons, it must be treated before disposed to landfill."

Jan 1, 2011

By Hong Liang-shi

Olivine lithium iron phosphate (LiFePO4) is considered as one of the most promising materials for lithium-ion secondary batteries because of its high theoretical capacity, low cost, good safety, benign environment and good cycle performance. In this paper, carbon-free and/or carbon-coated olivine lithium iron phosphate composite ultrafine powders were successfully synthesized from aqueous precursor solutions of (NH4)2Fe(SO4)2?6H2O, H3PO4 and LiOH?H2O by co-precipitation method. The obtained LiFePO4 or LiFePO4/C powders were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). Their electrochemical performance was investigated in terms of cycling behavior. As confirmed by X-ray diffraction and scanning electron microscope, the material obtained by co-precipitation within the temperature range of 60ºC to 100ºC and then followed by moderate heat treatment are a single-phase olivine LiFePO4with the particle size of about 300nm. An improved carbon-coated olivine LiFePO4/C material was prepared by adding conductive carbon materials, such as glucose, activated carbon and acetylene black, into the precursor. The carbon dispersed in the materials increases the electronic conductivity of LiFePO4/C composite, and consequently, leads to high rechargeable capacity of the material. The carbon-coated material with carbon amount of 7.64%wt obtained from glucose has the first discharge capacity of 150.3mAh/g at the rate of 0.1C and 129.3mAh/g at the rate of 1.0C, respectively. After cycled for 50 times, the capacity retention rate is 95.13% at the rate of 1.0C in the voltage range of 2.5 to 4.3 V vs. Li/Li+.

Jan 1, 2006

By V. Kamavaram

Ionic liquids are novel salts used as potential non-aqueous electrolytes for aluminum electrolysis at low temperatures. In the current research di-alkylimidazolium chloride ionic liquids such as 1-butyl-3-methylimidazolium chloride ([BMIM]Cl) and 1-hexyl-3-methylimidazolium chloride ([HMIM]Cl) were investigated for aluminum electrolysis. Melt formed by mixing ionic liquid with AlCl3 is termed as chloroaluminate and is composed of several polymeric chloroaluminate anions. Ionic liquids are studied as electrolytes for aluminum electrowinning and electrorefining of aluminum based materials (A356, A360, & Al-MMC) at low temperatures. Mechanism of aluminum electrodeposition in these chloroaluminate ionic liquid electrolytes was investigated using electroanalytical techniques such as cyclic-voltammetry and chronoamperometry. Aluminum electrodeposition on pure copper substrate in AlCl3-[BMIM]Cl (1.5:1.0) electrolyte at 30°C melts was found to be quasi-reversible process with a charge transfer coefficient ( of 0.40. Chronoamperograms obtained at different voltages in the range (-0.1 to -1.0 V) revealed that the initial stages of aluminum deposition in AlCl3-[BMIM]Cl melts was instantaneous nucleation followed by diffusion controlled growth of three-dimensional aluminum nuclei. The diffusion coefficient of electroactive species Al2Cl7¯ in AlCl3-[BMIM]Cl melts was found to be 6.5×10-7 cm2 s-1 from Cottrell?s equation and 3.9×10-7 cm2 s-1 from the dimensionless current-time transients.

Jan 1, 2006

By T. Manlyama

The Tamano Smelter of Hibi Kyodo Smelting CO., Ltd. went into operation in 1972. The Flash Smelting Furnace that was originally adapted was equipped with electrodes that were attached to the settler substitute of the slag cleaning furnace. Later the development of our own original coke combustion technology was promoted and a new Tamano Type Flash Smelting Furnace (T-FSF), without electrodes, was put into operation in 1988, T he technology of coke combustion and combustion the burner have continued to improve. As a result the copper losses in the Wag have been reduced as well as a stable operation has been achieved, Furthermore; this has been accomplished while increasing the concentration feed and the matte grade. The current objective is to continue to strive for high matte grade operation and to raise production efficiency while paying attention to the important subject of copper losses in the slag. In this report, the data related to the copper loss in the slag reduction are presented along with the influence of the thickness, settling time and coke. The recent operation conditions of the T-FSF are also presented.

Jan 1, 2003

By J. Brent Hiskey

Recently basic concepts of semiconductor electrochemistry and solid-state electronic structure theory have been applied to the dissolution of mineral electrodes. In this paper, fundamental aspects of semiconductor electro- chemistry and interfacial charge-transfer processes are reviewed. Information regarding the electronic and semiconductor properties of chalcopyrite is summarized. The electrochemical response of chalcopyrite in acidic solution is analyzed in terms of initial dissolution processes. The initial charge- transfer reaction involves the consumption of holes. It has been shorn that Fermi level pinning is consistent with observed electrochemical and dissolution behavior. Semiconductor electrochemistry has proved helpful in explaining the formation of intermediate surface films produced during the initial stages of chalcopyrite dissolution

Jan 1, 1993

By Xiang Lan

A strain of Thiobacillus ferruuxidans No. 8 was isolated from the acidic mine water of an arsenopyrite deposit, South China. It has been found from the experimental results that the growth of bacteria was inhibited by flotation agents. The order of toxic effect of different flotation agents on the growth of Thiobacillus ferrooxidans is ethyl xanthate > butyat ammonium aerofloat > butyl xanthate ? isobutyt xauthate >? flother No. 2 oil. The bioteaching treatment of arsenic and antimony-bearing gold concentrate in Longshan mine, Hunan province, China, was influenced considerably by the presence of flotation agents. The possible causes of the influence of flotation agents were discussed and an improved method was suggested.

Jan 1, 1991

By Thomas Niehoff, Yin Qing, Wei Zhongling, Liu Yongguo, Zhang Deliang, Tang Le

The gold ore of Shandong Gold Mining (Xinhui) was a refractory ore, which contained multi metallic sulfides (ZnS and PbS etc.) and carbonaceous. The gold ore concentrate came into leaching process and thickener and zinc replacement to recover gold. In order to improve gold recovery, the GOLDOX™ hydrometallurgy process was studied in Shandong Gold (Xinhui) by bench scale and 6 month plant scale test supported by Linde Gas. It was shown that the process promoted the leaching kinetics and improved gold recovery. The residue grade reduced 0.22 g/t in average after oxygen was applied. This indicates an operating profit increase 850,000 yuan/a in the plant. It was setting a good example for similar gold mine plant and would promote the oxygen application in Chinese gold mining industry.

Jan 1, 2015

By Kafui Nyavor

The indirect, and the direct contact mechanisms of bacteria oxidation of sulfides were studied using Thiobacillus ferrooxidans and pyrite. The aim was to determine which of the two generally aeeepted mechanisms played a dominant role, if any, during acid mine drainage (AMD) formation from the oxidation of sulfide minerals. The results show that at a pH of 4.5 where T. ferrooxidans are quite active, but where initial chemical oxidation of pyrite to Fe2+ is limited, the bacteria were unable to directly oxidize pyrite to any significant extent. Whereas, in the presence of Fe2+, T. ferrooxidallS assisted oxidation of pyrite by the indirect mechanism was observed and sustained over the pH and Eb range where the bacteria is active. The results lead to the conclusion that the direct contactmechanism of pyrite oxidition by T. ferrooxidans is insignificant. The predominant, and possibly the only, pathway involves the indirect bacteria oxidation of available Fe2+ to Fe3+, which in turn oxidizes FeS2 to generate additional Fe2+ and acidity in a cyclic process.

Jan 1, 1996

By Niander A. Cerqueira, Pâmela Berçot, Afonso G. Azevedo, Victor B. Souza, Victor T. Bartolazzi, Bruno Padilha

In recent years, concern about environmental issues has become a parameter to consider in the projects in engineering. In order to reduce the impact that the tire improper disposal may result for the environment, we sought a solution to this problem. This article proposes the use of rubber scrap tires as fine aggregate in concrete production. The material produced was analyzed by a bending test, resulting in product quality, in particular for application in situations requiring a more ductile material.

Mar 1, 2017

By Martin Reyes, Juan Hernández, Julio Cesar Juárez, Isauro Rivera, Ma. de los Ángeles Hernández, Francisco Patiño

The dissolution of Ag contained in metallurgical tailings was studied by adding ions Cu2+ and Zn2+ in S2O3 2- medium. Chemical analysis of mine tailings by cupellation revealed a Ag concentration of 71 g/ton. The XRF and XRD analysis confirmed the preponderance of SiO2 in the mineral matrix. The experimental dissolution process was conducted in alkaline solution using six concentrations of NaOH and five of S2O3 2-, at different temperatures, also using five concentrations of Cu2+ and Zn2+ as a catalyst. The results showed similar values for both systems (96.8% and 97.13%). The ion Cu2+ and Zn2+ increases the dissolution of Ag, and decrease the reaction time of dissolution. Under the conditions used, pH and stirring rate did not affect the dissolution of Ag.

Jan 1, 2015

By M. Sizgoric

Certain types of mineralogical alteration due either to weathering or serpentinization, and the effects these transformations have on the flotation of nickel sulfide ores are discussed. These effects are generally deleterious due to: (a) the poor flotation properties of the alteration minerals (as in the case of tochilinite), (b) the nature of the alteration texture (as in the case of violarite), or (c) .close association of the alteration products with other undesirable minerals (such as nickeliferous smythite). Several examples from INCO Metals Company's mines and mineral prospects are given as illustration.

Jan 1, 1981

By Krzyszof Borowiec

With the aim of determining the thermodynamic conditions for sulfation of impurity elements, in particular magnesium, in titaniferous slags the equilibrium gas composition for the sulfation reaction: MO + so2 + 1/2 02 = MS04 has been studied by an EMF technique with a solid zro2 + Cao electrolyte. Here M denotes the impurity elements: Mg, Ca and Mn, and the following _oxide systems have been studied: Ti02-MgO-Fe2 o 3 , Ti02-MnO-Mn2 o 3 , and Ti02 -CaO-Si02 , all in the . temperature range 700-1000ºc. Reproducible EMF values were obtained by adding small amounts of -Na2so4 to the oxide-sulfate mixture. From the observed results the Gibbs energy of formation of the phases Mg 2Ti04 , MgTi03 , MgTi 2o 5 , MnTi03 , CaTi03 , and CaTiSio5 , as well as the activity of MgTi05 in the solid solution with Fe2Ti05 have been calculated. The results show that, from a thermodynamic viewpoint, sulfation of these impurities in titaniferous stags i:s favorable- at around and below 800ºC.

Jan 1, 1985

By Allan J. MacRae

A copper alloy to be used for coils in cast copper cooling blocks has been identified and samples prepared for metallurgical examination and destructive testing to compare with cast cooling blocks manufactured from copper and nickel-copper alloy pipes. The copper alloy allows for the formation of a metallurgical bond between the pipe and the cast copper during the casting process, which does not normally occur with pure copper or nickel-copper alloy pipes. The alloy's coefficient of thermal expansion is also much closer to that of pure copper compared with nickel-copper alloys, so there is less strain induced at the pipe-cast copper interface due to differential thermal expansion. It is expected that this new pipe coil alloy and associated casting techniques will allow for the production of cast copper cooling blocks that have greatly enhanced service life in high heat load applications compared to existing technologies.

Jan 1, 2002

By Jose Hector Figueroa P.

Mexicana de Cananea, S.A de C.V. is a major copper producer mining a large deposit of the disseminated porphyry type considered one of the largest copper resources of the world with 2.7 billion tons of 0.60% copper for the mill plus 4.1 billion tons of averaging 0.26% copper for leaching. Mining of low grade sulfide leach ore, has been an important part of the overall production of the open pit mine which started in 1944. Before this time all the mining in Cananea was by underground methods. The leaching process in Cananea began on the 1920's with in situ operations in the underground mine and small dumps up to the 1950's. Large scale leaching operations began in 1960 and the copper solutions produced were treated in precipitation plants until 1,980 when the first SX/EW Plant was put in operation in Cananea. Leaching action is essentially ferric-bacterial, with no fiesh acid added to the leaching solutions. Traditionally, 5540% copper extraction is recovered fiom ROM, 70- 120 meter high leach dumps in 80 months of leaching. Cananea has successfully improved copper recoveries by implementing several actions that include: 1. Stripping of old dumps. 2. Leaching of old dumps through slotted casing. 3. Crushing conveying leach ore to minus 8 inch and stacking it in 30 meter lifts. As result of these actions, copper recovery has been increased' to about 70% of total copper with actions 1 and 2 and up to 85% in half the time by crushing-conveying the leach ore, based on the same solubility index of the run-of-mine ore. This paper describes the above actions that were implemented to enhance the leaching recoveries from. sulfide leach dumps and the economics of such actions.

Jan 1, 1999

By Thomas Havlik

It is proposed to realise the direct leaching, during which will be generated elemental sulfur and not sulfate or sulfuric acid as end product, under conditions that sulfur will not cover the leaching surface and Hot hinder the leaching course. The following improvements have been considered: -use of organic sulfur solvents -ultra high-frequency leaching -ultrasonic leaching -use of surface detergents or surfactants in leaching processes -simultaneously crushing and leaching These proposals are under investigation and preliminary results are promising

Jan 1, 1996

By Robert W. Bartlett

Hazardous metal contaminants in liquid and solid wastes and from ground spills are important environmental problems in many metallurgical production operations. Acid rock drainage, from mines and huge quantities of permeable mine waste, is probably the most ubiquitous example. Fixing mine waste contaminants in situ has been practiced, using sulfate reducing bacteria (SRB) and organic reagents as electron donors to create anaerobic conditions and precipitate metal sulfides. Aqueous solutions of sugar and alcohol have been percolated into mine wastes with good results. However, maintaining anaerobic conditions permanently is unlikely, as these solutions are eventually washed out of solid waste and contaminated ground by inflow of either groundwater or meteoric water, allowing re-oxidation from entering air. Emulsions of inexpensive, non-aqueous organic microdroplets dispersed in water provide earth wettablility equal to aqueous solutions and easy percolation into both the ground and mine waste. Subsequent breakdown of the O/W emulsion provides permanent retention of the organic phase, attached to earth particles, that secures lasting anaerobic conditions, precipitates metals as sulfides and prevents re-oxidation of these sulfides. This process and its optimization are described, including experiments with sand-filled columns representing a vertical section through solid waste. Results of organic and metal retention in solid waste are provided from analyses of acid mine water drainage before and after waste treatment.

Jan 1, 2006

By Motang Tang, Chaobo Tang, Shenghai Yang, Lulu Guo, Yun Li, Yongming Chen, Jing He

A new innovative process for one-step and cleaner extraction of lead from spent lead-acid battery by reductive sulfur-fixing smelting was presented. This paper summarized and discussed several potential sulfur-fixing agents and molten salts which can be used in this new technique. Thermodynamic analysis involving reaction mechanism, ΔGT and predominance-area diagrams of different smelting systems were performed, respectively. The results proved the technical feasibility and high-efficiency of this process. Copper oxide ash (CuO), zinc oxide ash (ZnO) and iron oxide bearing residues (FexOy) can be used as sulfur-fixing agent to extract lead through exchange reactions. Sulfur-fixed efficiency of CuO, ZnO and FeO decrease slightly in turn. Sulfur contained in PbSO4 is fixed in form of Cu2S, ZnS and FeS respectively which avoids SO2 emission. The addition of molten salt can significantly decrease temperature of reductive sulfur-fixing reactions. Molten salt can be regenerated and recycled in smelting system after filtering solid residues.

Mar 1, 2017

By Ian G. H. du Preez

It is illustrated how differences in the basic chemistry of individual metal ions can be exploited to develop new or improved separating agents. Factors like coordination number preferred by the specific metal ion, the degree of coordinate saturation reached by the metal ion and its relation to the phase transferability of the complex species, kinetic factors as opposed to thermodynamic factors controlling the success of the separation, the nature and type of the donor atom employed in a separating agent in relation to the preferences of the metal ion, the significance of stereochemical factors and the hydrophobicity of the media are some of the important factors which are discussed and applied for the development of pa1ladiwn(TI) and nickel(TI) specific separating agents, respectively.

Jan 1, 1999