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By R. W. Hammack

Results for the treatment of a problematic mining wastewater using bacterial sulfate reduction (BSR) are presented. Specifically, a BSR pilot treatment plant (250 L per day) was used to treat Berkeley Pit simulant to discharge standards with the selective recovery of separate Cu- and Zn-sulfide concentrates. Concentrates recovered in these tests contained greater than 50 % of the target metal and met specifications for sale to existing smelters. The biological component of the treatment was found to be surprisingly robust. Scaling and solid/liquid separation problems were encountered but considered normal for sulfide treatment. For Berkeley Pit water, capital costs for BSR treatment was found to be comparable to high-density sludge lime treatment. The value received from the sale of recovered copper ands zinc concentrates paid for all the operating costs.

Jan 1, 1999

By M. Rockandel

"Universal Dynamics Ltd. of Vancouver, Canada has developed, patented and commercialized the ""REMERC"" process for the treatment of mercury contaminated sludges and soils. Mercury is extracted into an acidified and oxidizing, sodium chloride brine solution. REMERC was initially developed to treat mercury contaminated EPA listed wastes (K106) generated by the chlor-alkali industry. More recent work has expanded the capability;' of REMERC to include remediation of mercury contaminated sites, equipment and building materials.In the process mercury is currently recovered from solution by cementation on iron powder in an agitated reactor. The process recovers high purity elemental mercury (99.9% purity). Cementation typically recovers about 90-95% of the mercury in 30 minutes. Higher recovery is not necessary because of the recirculation of the leach solution. When treating highly contaminated chloralkali wastes (5-13% mercury content), REMERC will reduce the mercury laden solutions from 400-1,000 mg/L mercury to 50-100 mg/L. In the treatment of less concentrated wastes «1,000 mg/kg mercury) such as those encountered in site remediation, the treated solutions will generally contain 10-20 mg/L mercury. Cementation while being simple and able to achieve the required recovery has the. undesirable properties of; requiring a solid-liquid separation and adding iron to solution which must be precipitated, ultimately increasing the weight of residue to landfill. .The potential advantages of electrolysis were recognized early in the development of REMERC. Mercury electrolysis is well known in gold and chloralkali processing. Initial testwork utilized a liquid mercury cathode and a coated titanium anode both common to chloralkali producers. The mercury cathode appeared susceptible to polarization and solution impurities significantly affected performance. Agitation of the mercury pool improved performance but it was still not possible to achieve the reduction objectives. Current efficiencies were low, near 10%, and it was apparent that a relatively large cathode pool would be required to limit the current density. A number of electrode combinations with and without a membrane were then tested in a vertical electrode' configuration but the desired performance was not obtained."

Jan 1, 1997

By M. I. Hoschke

The viability of pyrometallurgically treating zinc containing materials is enhanced by recovering zinc metal rather than oxide from furnace gases. During the history of zinc production, there has been continuing development on methods of recovering zinc metal that has resulted in three commercial designs in use today. The most widely used commercial technology, currently producing 13% of the world's zinc, is the lead splash condenser which is attached to the Imperial Smelting Furnace (ISF). The other remaining commercial designs are the zinc splash condenser and the Wheaton-Najarian vacuum condenser. The need to treat increasing quantities of secondary zinc materials, particularly Electric Arc Furnace (EAF) dust, has renewed emphasis on the development of ways to recover zinc metal. Development work in this area has proved to be difficult. Partly as a response to these difficulties, studies into the fundamentals of zinc condensation and absorption have been undertaken. Pasminco Research Centre (PRC), Newcastle, is also developing a. new zinc absorber to recover zinc metal from furnace gases:. The design attempts to address the problems associated with current devices.

Jan 1, 1994

By Lei Zhang, Shining Chen, Lina Wang, Pu Liu, Benquan Fu, Jiannyang Hwang

A PFS(polymeric ferric sulfate) coagulation-photocatalytic oxidation technology was used for advanced treatment of coking wastewater from secondary biological treatment. Effects of some key factors on TOC removal rate were investigated, and the results were compared with those of the common photocatalytic oxidation technology under the operating parameters of the photocatalytic oxidation defined. Single factor experimental results showed that TOC removal rate could reach 81%, when optimal operating conditions were as follows: TiO2 loading: 4.0g/L, irradiation time: 4h, initial pH is 5.1and PFS dosage:700mg/L. PFS coagulation and photocatalytic oxidation have synergistic effect, which is meaningful for highly efficient treatment of coking wastewater

Jan 1, 2015

By Jim Hardy, Tim McKnight

"The thermal mass flow controller, or MFC, has become an instrument of choice for the monitoring and controlling of process gas flow throughout the materials processing industry. In the semiconductor industry, these MFCs are used on over 70% of the processing tools. Reliability and accuracy are major concerns for the users of the MFCs. Calibration and characterization technologies for the development and implementation of mass flow devices are described. Sources of inaccuracy in process gas handling are described, and a model to correct for these inaccuracies is outlined. A gravimetric calibrator is described that allows flow sensors to be calibrated in corrosive, reactive gases to an accuracy of 0.3% of reading, at least an order of magnitude better than previously possible. All described capabilities are implemented in a Department of Energy User Facility which is available to industry and universities to test and develop gas flow sensors and controllers and evaluate their performance related to environmental effects, reliability, reproducibility, and accuracy.IntroductionMaterials processing is at the heart of semiconductor manufacturing. To make today's advanced integrated circuits, silicon wafers are subjected to over 200 process steps. Most of these steps involve processes such as etching, implanting, diffusion, annealing, deposition, and lithography (resist deposition and hardening). Often one or more process gases are used to complete the process step. To achieve the quality and performance required in the micro devices, accurate measurement and control of these gases is essential. The Oak Ridge National Laboratory (ORNL), in conjunction with the semiconductor industry, has been working to improve process gas measurement and control accuracy and reliability. Standardized test methods have been developed to characterize and benchmark the performance of mass flow controllers (MFCs), the method of choice for monitoring and controlling gas delivery. Testbeds have been designed and fabricated to produce repeatable and accurate data using these standards. Baseline testing was performed along with development of a unique mass flow instrument, the gravimetric calibrator."

Jan 1, 1997

By J. E. Murphy

Neodymium was electrowon into a Mg-Cd molten cathode at 650 °C from NdC1,-KC1 electrolyte. With the chloride system, neodymium was deposited into the molten alloy cathode until the neodymium concentration reached 20 wt pct. The alloy was then vacuum melted to remove the Mg and Cd. The current efficiency exceeded 80 pct under optimum conditions and the purity of the metal was 99.9 pct after vacuum melting. As an alternative approach, neodymium was electrowon at 1,030 °C from Nd,O, dissolved in a molten fluoride eleotrolyte. With the oxide-fluoride electrolyte, the metal was electrowon in a molten state with current efficiencies up to 60 pct. The purity of the metal was 99.8 pct with oxygen and carbon as major impurities. A number of problems were encountered including anode effect, low oxide solubility in the electrolyte, high neodymium metal solubility in the electrolyte, and reactivity of the metal with the cell materials. Approaches to improved cell, operation and prospects for commercial adoption of the electrolytic production of neodymium metal are discussed.

Jan 1, 1995

By V. A. Luganov

During the treatment of raw materials containing arsenic and antimony, problems in the distribution of these elements in the process products occur. In a number of cases in processing of copper-bearing materials, it is possible (or necessary) to obtain speiss. The purpose of the present research is to study the theoretical aspects and analyze the technological possibilities of producing copper-bearing speiss and the subsequent electrometallurgical processing with copper extraction as well as arsenic and antimony utilization. Copper arsenide (Cu3As) and copper antimonide (Cu3Sb) are the main components of the speiss. A thermodynamic analysis of the electrochemical oxidation of Cu3As and Cu3Sb, carried out using Pourbaix diagrams, showed that in a pH range from 0 to 2, oxidation potential 0.45-0.55V, ions of copper and arsenic and antimony trioxide are in the equilibrium. The kinetic study has shown, that with an increase in the polarization potential, the dissolution process changes from chemical to diffbsion control. An increase in temperature stabilizes the electrolysis process due to dissolution of arsenic trioxide forming on the anode. Electrolysis of speiss using a cathode diaphragm with the solution pH = 1-2, current density 150-200 A/m2 and temperature 60-70°C makes it possible to obtain cathode copper with a current efficiency of 95-96% and to remove the arsenic from the process during the electrolyte cleaning process. The arsenic content in the cathode copper did not surpass 0.002%. As the result of the research, a technological flowsheet for copper-lead speiss processing was developed. At the present time this technology is undergoing pilot testing.

Jan 1, 1999

By Shenghui Guo, Dongbo Li, Lijun Liu, Chengdong He, Jinhui Peng, Libo Zhang

In present study, partially stabilized zirconia (PSZ) was prepared by CaO doped fused zirconia heated by microwave furnace at the temperature of 1450 oC and holding time of 120 min. The XRD results showed that untreated fused zirconia mainly consists of crystalline compounds of cubic ZrO2 phase; while the roasted one mainly is composed of crystalline compounds of cubic ZrO2 phase and monoclinic ZrO2 phase. It is shown through the optimization of structures of two phases that structure of cubic ZrO2 and monoclinic ZrO2 reject each other, revealing its difficulty in forming coinciding interface and linkage of two phases being of Ca atom. Introduction Due to advantages of zirconia, such as high melting point, chemistry inertia, low heat transmission and so on. Zirconia is always taken as megathermal refractory material[1]. However, in the heating and cooling processes of pure zirconium oxide, martensitic transformation will take place associated with greater shear force and volume change, which severely limits the industrial application of pure zirconia in some areas. Such as: Refractory materials, grinding materials and high temperature insulation materials[2]. Through adding a certain amount of MgO, CaO, or Y2O3 stabilizer, etc.[3,4], the zirconia can change into fully stabilized zirconia, which exists in cubic phase. But this high purity fully stabilized zirconia cracks easily because of thermal stress. Therefore, the thermal shock resistance variation is one of the most important quality indicators of zirconia-based materials. According to the heat treatment, the fully stabilized zirconia can be changed into the partially stabilized zirconia (PSZ)[5], which exists in cubic phase and monoclinic phase and has superior mechanical properties, such as anti-heat, low thermal conductivity, large coefficient of thermal expansion and stability, as well as good wear resistance[6].

Jan 1, 2011

By Wenbo Luo, Kang Liu, Jilai Xue

"Coal fly-ash(CFA) from thermal power plants is rich in Al2O3, which has great potential as an alternative resource for alumina production. In this work, Alz03 contained in the coal fly-ash was extracted using an acid sintering-leaching process. This process was enhanced by aid of power ultrasound during the leaching. The recovery rate of Al2O3 was increased with ultrasound, compared with the similar process without ultrasound under the identical operation conditions. Leaching temperature can be lowered by about 10-l5°C and the processing time reduced by about 50%. The process kinetics were investigated in details for a better understanding of the fundamentals on the effects of power ultrasound. The obtained results demonstrate the potential application in reducing processing energy and increasing production rate.Introduction Coal fly ash is a typical solid waste generated from coal combustion in thermal power station. Vast amount of CF A accumulation lead to serious environmental problems such as air and water pollution, cropland occupation, radioactive contamination, etc. However, CFA is rich in Al2O3 and SiO2 content, so that it has a potential use as recourses for alumina and silica production [1]. Aluminum industry, especially in China, has made a rapid expansion in recent years accompanying with a large amount of bauxite consumption, resulting a urgent demand to develop secondary alumina resources like CF A to maintain a sustainable development of aluminum industry that faces grim challenge [2].Acid leaching is an efficient technology to use in alumina extraction from CF A. Since the particle of CF A is not naturally existed mineral but was formed in molten state at high temperature, the internal Al-O-Si bonds are so strong to separate alumina from the ash particle. Because of this reason, the direct acid leaching [3-6] operated at ambient temperature has low extraction efficiency, approximate 30% to 40%, which is attributed to self inhibition effect from CaS04 generated by reaction between CaO and H2S04 [7-8]. High pressure leaching can efficiently decompose mullite to release A12O 3 content in the fly ash particles, but this requires autoclave material having strong acid corrosion resistance, high temperature (100°C-300°C) and pressure (1.0MPa-2.SMPa) resistance while its operating security is low and its acid consumption is large [9]. Concentrated acid boil process is conducted at near acid boiling point (200 °C - 300 °C) in 4 mouth flask wrapped by electric heating jacket with high mass ratio of acid and ash to achieve high Al203 recovery rate from CFA. Its disadvantages are similar to the high pressure leaching technology except no-pressure, and also the operating solution at nearly boiling point acid may easily spill and splash with additional acid loss and potential safety hazard [10]."

Jan 1, 2014

By Qingzhu Li

The adsorption process of Pb2+ from aqueous solutions by spent grains modified with Imol/L NaCI solution was investigated. The effects of solution pH, contact time, adsorbent concentration, initial Pb2+ concentration, particle size on Pb2+removal were also studied. The initial adsorption process was rapid and 90.35% of Pb2+ adsorption occurred within 30 min. The absorption equilibrium was obtained at 4h. When pH was 5.5, Pb2+ concentration in aqueous solutions decreased from the initial content of 20 mg/L to 0.0 I mg/L after 5 hours by application of IOg/L adsorbent at 25?C, Pb2+ removal efficiency reached up to 99.95% and the Pb2+ remaining in aqueous solutions was under China Sanitary Standard for Drinking Water (GB5749-85). Adsorption data fitted well with Lanf+muir and Freundlich models. However,Langmuir isotherm model was better to descnbe Pb- adsorplion than Freundhch model, mdlcatmg that the applicability of monolayer coverage of Pb2+ on the surface of adsorbent.

Jan 1, 2008

By L. -C. Lai

A series of LaNi5-based alloys, with partial substitution of Ni by Al, Co, or V, were prepared The gas-phase hydrogen absorption kinetics and pressure-composition-temperature curves were measured The activation became easier and the plateau pressure was reduced as Ni was partially substituted by Al Substitution with Co reduced the hysteresis as well as the hydrogenation capacity, but enhanced the absorption kinetics Vanadium is often considered as a hydride former, but when it was added to LaNi5, it was found that V occupied the B site. A small amount of substitution of Ni with V led to a higher hydrogenation capacity and faster activation rate Based on these properties, an alloys LaNia 25CO0.5V0.1Al0. 15 was fabricated as an electrode. Compared with LaNi4.85Al0.15, it was found to exhibit faster activation, higher discharge capacity, and longer cycle life. The variation of the hydrogenation characteristics is discussed based on the physical and chemical properties of the alloying elements.

Jan 1, 1997

By Hiroshi Nakazawa

An acid mine drainage in abandoned Horobetsu mine in Hokkaido, Japan, contains arsenic and iron ions; total arsenic ca.10ppm, As(III) ca. 8.5ppm, total iron 379ppm, ferrous iron 266ppm, pH1.8. Arsenic occurs mostly as arsenite (As (III)) or arsenate (As (V)) in natural water. As(III) is more difficult to be remove than As(V), and it is necessary to oxidize As(III) to As(V) for effective removal. 5mL of the mine drainage or its filtrate through the membrane filter (pore size 0.45m) were added to arsenite solutions (pH1.8) with the concentration of 5ppm. After the incubation of 30 days, As(III) was oxidized completely with the addition of the mine drainage while the oxidation did not occur with the addition of filtrate, indicating the microbial oxidation of As(III). In this paper, we have investigated the microbial oxidation of As(III) in acid water below pH2.0.

Jan 1, 2006

By K. B. McTaggart, G. Owusu, P. J. Merrin

"This study was conducted at Hudson Bay Mining and Smelting's zinc electrowinning tankhouse to determine the effects of varying levels of antimony and continuous gelatin addition on current efficiency. The levels of antimony and gelatin were varied from 0.012 to 0.030 mg/l and 0 to 10 mg/ll2 • 31 respectively, based on neutral ZnS04 electrolyte. A non-linear mathematical model relating current efficiency with antimony and gelatin was produced. The optimum operating point for gelatin was 6.5 mg/l. On the other hand the current efficiency increased with decreasing antimony levels. An interaction term between gelatin and antimony is present but is not significant enough to improve the ability of the tankhouse to handle purification upsets in antimony. Individually, the current efficiency was linear (decreasing) with antimony, and parabolic with gelatin concentration. However, at low antimony concentrations stripping of the cathode sheet was difficult. IntroductionThe zinc electrowinning tankhouse at Hudson Bay Mining and Smelting was designed in the 1930's and consists of 120 rows with each row containing ten cells. This system cascades acid from cell to cell In a row, with neutral zinc sulphate solution added to each cell through manually controlled spigots. Animal glue additions are made manually three times per day by operations personnel. The problem with this type of cell design and operation is that feed solution flows and composition can vary from cell to cell and from row to row due to the large number of manual control points. A new system which reduces the number of manual control points was designed and tested to determine if improvement in control of cell conditions would affect current efficiency. This system mixes spent acid, neutral ZnS04 electrolyte and reagents (gelatin, antimony and strontium carbonate) in a separate mix tank, ensuring that all cells receive a uniform feed solution. Gelatin was used in the test system instead of animal glue (which is presently used) because of the poor solubility and supply of industrial animal glue. The study reported here is the first in a series of experiments designed to justify the need to modify the present cascading cell feed system (Figure 1) to the proposed feed system (figure 2)."

Jan 1, 1997

By In-Ho Chi

In copper metallization, resistivity of copper seed layer is very important since the thickness of seed layer is less than 200iun. Conventionally MOCVD has been used for this purpose however electroless copper plating is simple process and the resistivity of copper deposit is less than that of copper prepared by MOCVD. In this study eIectroless depositions of copper were conducted on different substrate to find optimum conditions of electroless copper plating for electronic applications. To find optimum conditions, the effects and selectivity of activation method on several substrates were investigated. The effects of copper bath composition on morphology were investigated. The effects of pH and stabilizer on deposition rate was investigated. The resistivity of copper with thickness was also measured.

Jan 1, 2001

By V. A. Shumsky, I. P. Polyakov, N. M. Ospanov, M. A. Lyamina, N. N. Ushakov

Studies on the kinetics of the competitive processes of PbS volatilization and PbS oxidation, as applied to the heat and mass transfer conditions in the flame of the Kivcet furnace, revealed that the rate-determining factor is the supply of heat. Therefore, low yields of fume in the autogenous flash smelting of lead sulphide feeds are noted despite the high volatility of PbS at 1,300-1,400°C. Dust formation in the autogenous flash smelting of Kivcet-smelters does not exceed 5-7%, of which fumes amount to ~ 80%. Using extra fuel during autogenous smelting involves the mismatch of the sulphide oxidation rate and the release of heat in the flame, and increases the fume yield. This is a major cause of the high dust formation in pilot plant trials. The analysis of dust formation in the Kivcet smelting of oxidized lead feeds in an industrialscale smelter shows an overall increase of dust formation (up to 10% of the feed), with fumes constituting ~ 80% of the dust. A pronounced increase of the zinc component of the fumes is also noted. Lead

Jan 1, 2000

By W. G. Davenport

All Outokumpu flash furnaces burn some hydrocarbon fuel. Hydrocarbon combustion supplements heat from Fe and S oxidation and provides local heating in cool; parts of the furnace. Adjustment of hydrocarbon fuel combustion rate is an effective way of controlling furnace temperature. More oxygen and more oxidation of Fe?and S in the flash furnace continue to diminish the need for1hydrocarbon fuel. Still, as Tables 2.1 and 3.1 show, all flash furnaces use it. Oil is the most common fuel -natural gas, coal and coke are also used. This chapter demonstrates how hydrocarbon fuel is included in our flash furnace matrix. It shows that: (a) three new variables, mass hydrocarbonfoel. mass CO2 in offgas and mass H2O in offgas are inserted (b) carbon and hydrogen balances are added (c) hydrocarbon fuel quantity is specified (d) ,the oxygen balance is modified to include CO2 and H2O (e) the enthalpy balance is modified to include hydrocarbon fuel, CO2 and H20.

Jan 1, 2001

By Toshihiro Kuzuya

A hydro metallurgical process has been developed for the recovery of metal values such as Co, Ni and rare earths from the electrode materials of spent nickel metal-hydride(Ni-MH) secondary battery. MmNis_xCo. (Mm : Misch metal) intermetallic compound could be separated from the electrode materials mixture by sedimentation. A typical chemical composition of MmN5-xCox was approximately, in mass%, 56.0%Ni, 13.4%Ce, 10.6%La and 7.9%Co. The time dependency of leaching intermetallic compound with sulfuric acid solution was examined with processing factors such as sulfuric acid concentration, temperature and agitation intensity, The leaching of rare earth metals proceeded very rapidly, reaching completion in less than 1.8ks. On the other hand, the slow leaching of nickel was observed. The percent of nickel leached at 328K could only reach about 70%.

Jan 1, 2003

By Ulrich E. Klotz, Gemot Pottlacher, Shahid Mehmood

"Platinum alloys are frequently used in technical applications and in jewellery. Their thermophysical properties such as density, heat capacity, thermal conductivity and surface tension play an important role in casting processes and are required as input data for casting simulation. Scope of this work was to investigate these properties by different methods. Platinum and four alloys namely, Pt96Cu4, Pt68Cu32, Pt50Cu50 and Pt25Cu75 were investigated. Melting range and thermal expansion was measured at fem by DSC and dilatometry, respectively.At TU Graz wire shaped samples were investigated by an ohmic pulse heating technique. This technique allows the calculation of specific heat capacity and the temperature dependencies of electrical resistivity, enthalpy, and density of these alloys in the solid and liquid phase. Experimental results were compared with available literature and data from thermodynamic calculation using the SNOBl database and ThermoCalc.IntroductionPlatinum is a precious element and its alloys are commonly used in jewellery. But Platinum is much more difficult to cast then other jewellery elements like silver or gold, because of its high melting temperature, large shrinkage during freezing, low thermal conductivity, high surface tension, and high viscosity. As a result there arise problems during casting. Hence to resolve these difficulties a detailed study of thermophysical properties of solid and liquid platinum and its alloys is necessary for simulation and casting. The Platinum alloy samples were prepared by vacuum induction melting and casting into copper molds. Rods of 3 mm in diameter and a length of 80 mm were prepared and drawn to wires of 0.5 mm in diameter."

Jan 1, 2011

By C. T. Philipp

Recycling of waste is much preferred over disposal. This paper discusses the Enviroscience, Inc. (ESI) process, now being commercialized by MetWool, Inc., to recycle hazardous wastes using an extractive metallurgical process which is followed by vitrification of non-reducible metal oxides. In this process, volatile and reducible metals are reclaimed as their respective oxides and elements.

Jan 1, 1995

By K. C. Mills, P. N. Quested, A. P. Day, R. F. Brooks

"Methods have been developed to measure the physical properties of molten materials relevant to the fluid flow in high temperature processes. Data for the densities, viscosities and surface tensions of Al-, Ni- and Fe-based alloys are compared with (i) values for the pure metals and (ii) estimated values obtained from models making use of chemical composition of the alloy. Experimental values for metallurgical slags are also given and compared with estimated values.1 IntroductionPhysical property data has proved very useful in improving process control and product quality. For instance, in the continuous casting of steel the viscosity (TJ) of the mould flux is important since it determines (i) the optimum casting conditions, nVc = 2.5±1 dPas (m min-1) where V c is the casting speed and (ii) the level of slag entrapment (which leads to inclusions) in the metal. Thus data for properties like viscosity are exceedingly useful in understanding the process and the problems encountered and the causes of defects and problems.Another interesting development which has helped to increase our knowledge of processes and improve process control and product quality is the development of mathematical models of the fluid and heat flow in the process. These models have been developed to the stage where one of the prime requirements is for good physical property data for the industrial materials involved. Recently, Oxley [1] has shown that the use of reliable, experimental, property values for the commercial alloy in a commercial software package produced a significant improvement in the prediction of casting defects. Thus reliable property data are required for liquid metals but also for (i) liquid slags since many processes involve the use of a slag to refine and protect the metal or to lubricate the mould and (ii) refractories, sand and investment moulds."

Jan 1, 1999