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By S. P. Rivers

The stainless steel industry re1ies on nitric-hydrofluoric acid (HNO,/HF) pickling solutions to remove surface contaminants and maintain the corrosion resistance of the steel. More stringent environmental guide1ines are expected to be placed on the disposal of these solutions which could significantly increase processing costs. The U.S. Bureau of Mines has been conducting research to develop a process for recycling depleted pickling solutions, thus reducing the quantity of by product acids generated. Research has shown that F- can be liberated from the predominant iron fluoride species (FeF,') by using oxalic acid in an electrodialysis cell. Ion selective membranes allow dissolved metals in the depleted solution to be replaced with hydronium ions by metathesis, thereby regenerating the HF. The regenerated HN03/HF is then retained in the pick1ing solution. This paper reports on the research effort at the U.S. Bureau of Mines Rolla Research Center to apply electrodialytic recycling to HN03/HF pickling solutions.

Jan 1, 1993

By S. L. Pohlman

Physical characteristics of possible importance in the acid leaching of Chrysocolla have been evaluated. Surface area studies and pore size distribution indicate: 1) a large surface area (350 m /gm); 2) an average pore size of 13 or 16 Å , depending upon use of the adsorption, or desorption, branch of the Type IV isotherm in the evaluation; ) the presence of a significant fraction of pores of size less than 15 Å determined by the accumulation surface area method. The initial structure is micro- crystalline on the basis of x-ray powder patterns; the silica leach residue is amorphous and has only 24 m2 /gm surface area, and loses integrity when dry. However, readsorption of copper onto the wet leach residue gives a product with integrity and 100 m2 /gm surface area. Visual observation of the leach residues supports evidence of a non-protective diffusion mechanism of leaching which is well correlated by the shrinking core model previously presented.

Jan 1, 1976

By Sepp Härkki

The energy crisis in Finland after World War I1 together with a sharp rise in the price of energy caused Outokumpu Oy to consider replacing the electric furnace smelting of copper concentrates by some other method. The flash smelting method developed under these circumstances offered a considerable saving of fuel through the utilization of the reaction heat of sulphides and yielded a high recovery of sulphur in the form of acid. The pilot plant testing of the new process was carried out in the years 1947 - 1948. The process was adopted for the smelting of copper concentrates (1) (2) (3) on a commercial scale in 1949 and applied successfullv to the smelting of -nickel concentrates' at the Harjavalta Works in 1959 (4) (5) (6). In 1962 Outokumpu adopted another type of flash smelting where elemental sulphur is recovered from the gases after the thermal decomposition of pyrite in the flash smelting furnace (7) (8): In recent years, the copper-nickel flash smelter and pyrite process have been combined to produce elemental sulphur instead of SO2 from the smelter gases (9) (10). The basic idea of the Outokumpu flash smelting process for sulphidic ores is that the conventional methods with separate roasting and smelting operations are replaced by a combined roasting, smelting and part-converting process carried out in one unit. The heat generated from the exothermic reactions can thus be used for smelting the ore so that only a small amount of additional fuel is needed. The characteristic of the method is also that the dried, fine-grained concentrate is smelted in suspension, which offers the best conditions for rapid reactions. The recovery of waste heat from the furnace off-gases had been considered already in the original flash smelting system. A

Jan 1, 1976

By Shaik Jeelani, Esperidiana A. B. Moura, Vijaya K. Rangari, Roberta A. Lima, Rene R. Oliveira

This work present the preparation and characterization of biodegradable nanocomposites based on aliphatic-aromatic copolyester (PBAT)/polylatic acid (PLA) blend reinforced by TiO2 nanoparticle. The biodegradable polymeric nanocomposites were prepared by melting extrusion process using a twin-screw extruder machine. The influence of the TiO2 nanoparticle addition on mechanical and thermal properties of PBAT/PLA blend was investigated by tensile and impact tests, SEM, DSC and XRD analysis and the correlation between properties was discussed.

Jan 1, 2015

By Kohei Yajima

The dusts and fly ash generated from the steelmaking processes and municipal solid waste incineration processes contain metallic elements such as Fe, Zn, Pb and Cd with considerable amount of halogens. In Japan, zinc in dusts is recovered by Waelz kiln or MF process, etc. However, the presence of halogen in the dust affects the evaporation and condensation behavior of zinc and other metals, and disturbs the direct recycling of dust to steelmaking processes, because alkali or heavy metals reacted with halogen vaporize easily as halides and/or oxyhalide compounds in pyrometallurgical process. Recently, the formation mechanism of zinc oxychloride vapor was investigated and the formation of zinc oxychloride such as ZnOCl was proposed. However, considering the practical operation, the effect of water vapor on the evaporation behavior of oxychloride is not fully clarified yet. This study is focused on the investigation of evaporation behavior of ZnO with Ar- O2-HCl-H2O atmosphere.

Jan 1, 2008

By Paul O. Malan

"The Tusc gold deposit is located along the Carlin Trend approximately 13 kilometers north of Carlin, Nevada and 2.5 kilometers northwest of the Gold Quarry mine. Tusc is one of several structurally controlled oxide gold deposits located along the Good Hope fault within the Maggie Creek subdistrict. Mining commenced in 1994 with an oxide reserve of780,000 troy ounces of gold at an average grade of 1.34 g/t Au. The Good Hope fault forms the southwestern edge of the Schroeder Mountain uplift (also known as the Carlin Window) and juxtaposes carbonate rocks of the Siluro-Devonian Roberts Mountains Formation against siliceous mudstone, siltstone, and silty limestone of the Devonian Rodeo Creek unit. Submicroscopic gold mineralization is disseminated in the Good Hope fault system and in fractured hanging wall carbonate rocks. Wallrock alteration includes silicification, deca!cification, sericitization, and late alunite replacement and veins. All Tusc ore is transported 2.5 kilometers to Gold Quarry for processing. Leach-grade ore (0.2 - 1.7 g/t gold) is placed on the oxide leach pads, and mill-grade ore(> 1.7 g/t gold) is processed through the CIL oxide mill. IntroductionThe Tusc gold deposit is located in Eureka County, Nevada, U.S. A, approximately 13 kilometers north of the town of Carlin and 2.5 kilometers northwest of the Gold Quarry mine (Fig. 1 ). Tusc is one of several open-pit, oxide, gold deposits within the Maggie Creek subdistrict of the Carlin Trend. Tusc is a structurally controlled gold deposit located along the Good Hope fault. Submicroscopic gold mineralization is disseminated in the brecciated and silicified Good Hope fault zone and along intersecting northeast and northwest striking structures."

Jan 1, 1997

By Guoqiang Lv, Xi Yang, Wenhui Ma

Cast multicrystalline silicon ingots are widely used in photovoltaic manufacturing. A key issue to achieve high solar cell efficiencies is to attain an optimized temperature field during directional solidification (DS) process. This paper reports numerical investigation of multicrystalline silicon (mc-Si) ingot production using two major types of DS furnace. Specific examination is made on thermal distribution, interface shape and stress field. Evaluation is performed for the applicability of thermal system design to reduce thermal stress, improve crystal quality and enhance energy efficiency. The effects of procedure parameters and geometric configuration on temperature distribution are discussed as well to provide the viable solutions for systems optimization.

Jan 1, 2015

By John P. Hager

One possible approach for the recovery of mercury from acid plant blow-down sludge in smelters is the use of a vacuum retort reactor for the vaporization of the mercury with subsequent collection of metallic mercury in an attached condenser. An experimental study was undertaken to investigate the vaporization of mercury when present as a compound in the Hg-S-O and Hg-Se systems. A transpiration reactor was modified to operate under reduced pressure and with a continuous flow of inert sweep gas. A water-cooled cold finger was inserted into the exit end of the reactor to provide for the rapid quenching of the exit gases and the collection of the mercury. Rates of vaporization were measured at several temperatures for each compound and were generally found to be constant at a given temperature and reactor pressure. The results were used to determine the minimum operating temperature for 100% vaporization of the compound in 60 minutes. For Hg2SO4, HgSO4, and HgSO/2HgO the required temperatures. for a reactor pressure of 50 Torr. were determined to be 634°, 622°. and 603°C. respectively. For HgO, HgSe, and HgS the required temperatures were 557°. 451°. And 382°C. respectively. For HgS the rate of vaporization was also measured at a reactor pressure of 1 00 Torr. The rate of vaporization was found to be slower resulting in an increased vaporization temperature of 423°C. It was also determined that the mercury vapor present in the exit gas stream can back-react with the other gas species to a significant extent and can result in very little condensed metallic mercury. For the vaporization of both HgS and HgSe. the mercury vapor was found to have back-reacted to the extent that virtually none of the vaporized mercury was collected in metallic form. For the vaporization of Hg2S04? HgS04, and HgSO4*2HgO the amount of metallic mercury recovered varied from approximately 50% for HgS04*2HgO to approximately 10% for Hg2S04 and HgS04. Only for HgO was the recovered mercury in primarily elemental form. The application of the results to the operation of a vacuum retort and condenser system is discussed.

Jan 1, 2001

By B. Ozturk, K. Ito, R. J. Fruehan

"A simulation model for bath smelting processes for the production of iron was developed which predicts the coal, flux, ore, and oxygen consumptions and the off gas volume, temperature and composition. The model is comprehensive in that it takes into account all of the important variables including coal composition, metal composition, ore composition, slag basicity, post combustion ratio, (PCR), prereduction degree (PRO), heat transfer coefficient (HTC) , flux, scrap charge, and heat losses. Four basic cases were considered: I. 30% PRO-50% PCR; II. 90% PRO-O% PCR; III. 60% PRO-30% PCR; and IV. 0% PRO-50% PCR. Several different coals were considered and a sensitivity analysis of the critical variables was performed. The model also estimates the sulfur content of the metal. The major conclusions included:1. Post combustion significantly reduces coal consumption but above 20% PCR little reduction of FeO to Fe can be performed with the off gas.2. Prereducing to FeO (Case I) and having as much post combustion as consistent with good heat transfer is an attractive process. This process only requires a simple pre reducer, uses less coal, and is relatively insensitive to the type of coal used.3. High off gas temperatures may pose a potential problem. The off gas temperature can be reduced by using an 02-Air mixture for post combustion, limiting post combustion or adding water to the gas.4. The use of CaC03 in place of CaO or of supplemental electricity does not appear attractive.5. The melting unit is theoretically an energy efficient scrap melter. For Case I using 200 kg of scrap as part of the charge the coal consumption decreases by about 80 kg.6. With PCR > 30% the FeO content of the slag is expected to be 2-5%, and the metal will not be saturated with carbon. These factors and the increased sulfur load since coal is the fuel indicate the sulfur content of the metal may exceed 0.25%"

Jan 1, 1988

By O. Ryosuke Suzuki

A new metallurgical process via sulfide is proposed: a sulfide is produced at a high temperature from its metallic oxide using gaseous CS2, and this sulfide is electrochemically reduced to its metallic state using molten salt. This combined process via sulfide is effective to obtain high purity of metallic powder, even if the metal in its oxide is strongly combined with oxygen. For example, it is not easy to reduce stable oxide TiO2, and only Ca can remove oxygen to form α-Ti. However, a fairly large amount of oxygen remains as Ti–O solid solution. Because the solubility of S in Ti is very small, this proposal was examined experimentally both on the conversion of TiO2 to TiS2 and on the successive reduction of TiS2 to Ti. TiO2 powder was exposed to CS2 gas flow at 1073 K, and the conversion to TiS2 was confirmed. TiS2 could be reduced to Ti powder either by calciothermic reduction or electrolysis in a CaCl2 melt. By Ca reduction at 1133 K in CaCl2 melt, sulfur concentration decreased to 0.03 mass%S when the amount greater than twice the stoichiometric calcium amount is added. By electrochemical reduction at 1173 K in CaCl2–CaS melt, S concentration significantly decreased to 0.01 mass% S when four times larger amount of electric charge was supplied.

By Shaik Jeelani, Mahesh Hosur, Esperidiana A. B. Moura, Rejane D. Campos, Emilia S. M. Seo, Kerry Kirwan, Francisco R. V. Díaz, Maria Sotenko

The use of natural fibers with polymeric resins has spread rapidly. In order to improve the mechanical properties of material, in this work, two variables were used: mercerization and electron beam irradiation. This paper describes the preparation and characterization of biocomposites that were prepared in two different routes using green high density polyethylene (HDPE) and Brazil nut pod fiber (BNPF): the first was to irradiate the composite with 150 kGy and the second was to irradiate the matrix with 15 kGy followed by composite preparation. In both cases mercerized and non-mercerized fibers were used. The irradiation process was carried out using a 1.5 MeV electron beam accelerator, at room temperature and in the presence of air. The material was characterized to evaluate the effect of treatment on mechanical properties of material.

Jan 1, 2015

By Marietta Canty

A paper is presented in which an innovative biological process is described for the treatment of cyanide-, metals-, and nitrate-contaminated mine process water. The technology was tested for its ability to detoxify cyanide and nitrate and immobilize metals in wastewater from agitation cyanide leaching. A pilot-scale demonstration is described in which a pilot plant was constructed to demonstrate the technology on a mine process waste stream at a mine in Nevada. The demonstration was performed Jointly under the Mine Waste Technology Program (MWTP), which is funded by the U.S. Environmental Protection Agency (EPA) and is jointly administered by the U.S. Department of Energy's (DOE) Western Environmental Technology Office (WETO) and the Superfund Innovative Technology Evaluation (SITE) Demonstration Program under Interagency Agreement Number DW89938513-0 I-0. MSE Technology Applications, Inc. (MSE) located in Butte. Montana, was the contractor responsible for conducting the project, and Pintail Systems, Inc., of Aurora. Colorado, was the technology provider. The pilot-scale unit was field-tested at the Echo Bay McCoy/Cove Mine southwest of Battle Mountain, Nevada. The biotreatment process was considered to be successful in destroying cyanide in the mine process water. The process was also determined to be effective in removing metals. The pH was consistently neutralized, and nitrates were successfully removed from the mine process water. As a result of conducting these pilot-scale tests, the biotreatment process was concluded to be an innovative, cost-effective alternative for the treatment of mining wastewaters.

Jan 1, 1998

By E. Burgos Cruz

The behaviour of S, N and P during refining of Fe-18 wt%Cr-10 wt%Ni with calcium carbide was investigated. The effects of the initial contents of C and N in the metal phase, as well as the supply method of calcium carbide to the melt on the removal degrees of S and P were evaluated. Heats were carried out at 1873K, in MgO crucibles, using a laboratory induction furnace. It was observed that simultaneously with S and P, N and O have also participated in the reactions. It seems that, in fact, O governs the behaviour of the other elements dissolved in the melt and that N is had to the removal of P with calcium carbide. It was also noticed that high C content in the metal phase have not altered the dephosphorization and desuffirization degrees, but that the supply of calcium carbide done by injection led to a lower dephosphorization degree than the one obtained by dumping it.

Jan 1, 1995

By N. Choi

The distribution behavior of cobalt, gold, and silver in nickel sulfide smelting was investigated between 1250-1300 °C under inert gas atmosphere. The distribution coefficients of these elements between nickel-copper-iron matte and silica-saturated iron silicate slag were determined as a function of matte and slag compositions. The effect of slag additives such as CaO, MgO, and Al2O3 on the solubility of cobalt, gold, and silver in slag was also investigated. It was observed that the distribution coefficients of these &nor elements were strongly dependent on matte grade. For cobalt and silver, the distribution coefficients decreased as the matte grade increased. However, the distribution coefficients of gold increased as the matte grade increased. The solubility of these minor elements in iron silicate slag was considerably decreased by the addition of basic oxides. Temperature dependence of the distribution of the minor elements will also be discussed.

Jan 1, 1995

By Matti Hämäläinen

Outokumpu has developed a new chloride leaching process, HydroCopper?, for copper concentrates. The process utilizes the cupric ion as oxidant, which is able to dissolve chalcopyrite. After solution purification monovalent copper is precipitated as cuprous oxide, Cu2O, using sodium hydroxide. Copper product is produced from Cu2O by reduction, melting and casting. An essential part of the new process is chlor-alkali electrolysis, which regenerates the reagents used. All impurity metals are removed before Cu2O precipitation, because otherwise they would report to the copper product, impairing its quality. A multistage solution purification scheme has been developed consisting of firstly, chemical precipitation of impurity metals by pH increase, secondly, cementation of silver and thirdly, removal of trace multivalent ions using ion exchange. This paper describes the characteristics of solution purification in the HydroCopper? process based on the laboratory tests and pilot runs made by Outokumpu Research Oy.

Jan 1, 2003

By K. Osseo-Asare

Aqueous stability diagrams (25°C) are presented for the systems M-H2O and M-Oxalate-H2O where M=Sm, Nd, Co, and Fe. With the aid of these diagrams (i.e., Eh-pH and log[Metal]- log[Oxalate]), the solution-chemical constraints on metal dissolution and precipitation are identified. By comparing the corresponding stability diagrams, conceptual flowsheets are developed for metal recovery from Sm-Co and Nd-Fe-B magnet scrap.

Jan 1, 1997

By Takahiko Okura, Satoshi Okano, Hiromichi Takebe

"Fine zinc concentrates tend to become sticky when roasted in a fluidized-bed reactor. The oxidation of high-purity ZnS powders and ZnS concentrates with different particle sizes were studied in terms of phase changes and particle morphologies. The sample materials were directly oxidized to ZnO in a roasting process performed over 700°C. Zinc oxide particles with diameters less than 0.5 ìðé formed at 700°C; the particle size increased by grain growth at 900°C. The coarse ZnS concentrate formed the oxysulfate ZnO2ZnS04 when roasted at 700°C; the sulfate transformed to ZnO at higher temperature.1. IntroductionRoasting is an important step in zinc extractive metallurgy because more than 80% of the world's zinc is produced from zinc sulfide concentrates using the roast-leach-electrowinning [1,2]. Currently, zinc concentrates with a finer particle size distribution are used to enhance recovery rate. However, the finer zinc concentrates tend to produce a sticky calcine in a fluidized-bed roaster [3].The factors that affect products in a fluidized-bed roaster include particle size, contaminant, O2 and SO2 partial pressures, and the feeding method of ore to the roaster. This study examined roasting behavior of high-purity ZnS powders and ZnS concentrates with different particle sizes. The phase changes and particle morphologies of the calcine samples producted from theZnS powders were studied."

Jan 1, 2012

By Hande Cavus, Ibrahim Yusufoglu, Cem Kahruman

"In this study, ammonium tetramolybdate (ATM) was obtained as the intermediate product of ammonium heptamolybdate tetrahydrate (AHM). The thermal decomposition mechanism of ATM was investigated under nonisothermal and isothermal conditions in air and inert gas atmospheres. Nonisothermal experiments were carried out by TGA/DTA/MS while TG was used for isothermal conditions. Characterization of the decomposition products were carried out by XRD and FT-IR. The thermal decomposition of ATM in air proceeds in a single step and forms M0O3 while [(ÍÇ4)2è]ïïï83Ìïè3 and molybdenum suboxide (Ìïè3.÷, ÷=0.025) were obtained in the first and the second steps of thermal decomposition in He, respectively. Activation energies, frequency factors and kinetic model equations were determined for thermal decomposition reactions. Fractional conversion-time diagrams were compared with diagrams drawn according to kinetic model equation.IntroductionM0O3 is usually used as catalyst in industry [1]. AHM is the basic source to produce molybdenum containing catalysts used in petrochemistry [2]. The oxides of Li, V, W, Te, Bi and Sn are doped in M0O3 to produce catalysts, which find commercial applications in the industry. The properties of M0O3 are affected by dissolution, settling, calcination, drying and thermal decomposition processes [1]. There are several studies in the literature about the thermal decomposition of AHM and the characterization of the decomposition products in different gas atmospheres and at various heating rates [3-19]."

Jan 1, 2012

By Alexandre Bonan

This paper reports the results of a kinetic study on the oxidation of free cyanide and Cu-cyanide complex ions with HO,. The variables and respective ranges studied were the following: [CN] total =10 - 500 mg/l; pH=10-11; (H2O2/CN) mole ratio = 1- 3; (Cu/CN) mole ratio = 0.10 - 0.25. The results were interpreted by a semi-empirical model that incorporates the useful oxidation reactions and the parallel alkaline decomposition of H2O2

Jan 1, 1994

By T. T. Chen

Secondary copper anodes are generally rich in Sn, Pb, Ni and Sb, but are notably deficient in Se, Te and Ag. In the secondary copper anodes, most of the Ni, virtually all of the Ag, slightly more than one-fifth of the Pb, about one-third of the As and Sb, and approximately one-tenth of the Sn are in solid solution in the copper. The remaining impurity contents occur as 1-5 µm grain-boundary inclusions in the anodes, and these are mainly Cu2O, SnO2, Cu-Pb-As-Sb-Bi oxide, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide, Cu-Sb-Ni oxide (Kupferglimmer) and trace Cu2(Se,Te). Barium sulphate, which originates from the mold wash used in casting, is also present in the anodes. During electrorefining, the BaSO4, SnO2, Pb-Sb oxide, Sn-Ni-Zn oxide, Cu-Sn-Ni oxide and Cu- Sb-Ni oxide inclusions are liberated and accumulate in the slimes layer. Solid solution Ni dissolves and the Ni accumulates in the electrolyte. Solid solution Sn and Pb dissolve, but partly reprecipitate as Sn arsenate and PbSO4, respectively. Solid solution Ag dissolves but rapidly reacts to form Ag2(Se,Te), Ag powder, Ag-bearing Cu2O, (Cu,Ag)SO4 or a complex oxidate phase. Partial dissolution of the Cu-Pb-As-Sb-Bi oxide particles takes place; the Pb component is converted to PbSO4, whereas Cu, As, Sb and Bi dissolve. The reacted particles retain the morphology of the original Cu-Pb-As- Sb-Bi oxide phase. Some of the solubilized As, Sb and Bi remains in solution, but much reprecipitates as SbAsO4, As-Sb-Bi oxide, and as a poorly defined oxidate phase which consists mostly of Cu-Ag-Pb arsenate-sulphate. The high Sn contents of secondary copper anodes do not seem to affect the behaviour of the anodes during electrorefining.

Jan 1, 1999