Search Documents

By R. Mehta, M. Misra, X. Su

"The conventional methods to assess Acid Mine Drainage (AMD) potential of the waste rocks and tailings are based on wet chemistry and leachability tests. These methods are time consuming and expensive. There is a growing interest to develop alternate techniques to establish the reactivity of acid mine tailings and stability of treated waste forms. The Electrochemical Impedance Spectroscopy (EIS) is a reliable non-invasive technique which can be used for quick estimation of reactivity of the potential acid generating tailings. In this paper the utilization of the EIS technique for the estimation of reactivity of tailings is discussed. EIS can also be used to predict the long term stability of different stabilized waste forms.IntroductionMetal contaminated mine drainage is one of the most persistent environmental problems facing the mining and mineral processing industries today. Of all the mine drainage pollutants, acid mine drainage has become a substantial concern because of the potential long-term environmental implications and the accompanying liabilities. The main source of acid mine drainage is the tailings containing sulfide-ores which are generated during the ore processing. When these sulfide minerals, particularly pyrite and pyrrhotite, are exposed to oxygen and water they begin to oxidize. The initial chemical reactions produce acid and the acid dissolves heavy metals present in the tailings. Rainfall and snow-melt flush the toxic solutions from the waste sites into the downstream environment [1-2]. In addition to mining tailings, several Department of Energy (DOE) sites contain wastes which are contaminated with radionuclides and heavy metals."

Jan 1, 1999

By Jingbo Liu, Zhimin Wang, Wenchao Li

"IntroductionThe advantages of non-stoichiometric perovskite material are highlighted in many papers[l]and many of this family of materials are well-suited to integration into microsensor devices. Among them, barium titanate is the most promising due to it's piezoelectric, pyroelectric, dielectric properties. Through modification, BaTiO3-based materials can be utilized in many kinds fields, such as surface wave probe; pholoconducting devices, field-effect transistor, permanent memory permanent storage, and ultrasonic transducerl2-3l. In this Paper, a series of BaTiO3-based polycrystals were synthesized by sol-gel processing which appears to be a very promising method for the manufacture of ceramic, because it offers significant advantages such as high purity, chemical homogeneity, controlled particle sizes of ceramics, and lower processing temperatures [4]. In a sol-gel process, alkoxides of the constituent elements show different reactivity toward water so that the preparation of multi-component homogenous system is difficult. In the experiment, inorganic salt was substituted for some of the alkoxides. Acetic acid which is employed for the solvent and catalyst, acts as donor ligand to titanium alkoxide and controls, the hydrolysis polycondensation reaction. Taking these aspects into consideration, we select the system Ba(OAc)2, , La(OAc)3, Ti(O11Bu)4 and acetic acid which is used as both solvent and homogeneous catalyst for the first time.ExperimentalA series of La3+-doped BaTiO3-based nano-crystals were prepared with sol-gel technology using various parameters. The precursor solution was prepared in the presence of barium acetate, lathanium acetate, and titanium tetrabutoxide monomer in butyl alcohol. According to the flow chart (fig. I.), Ba(OAc)2, La(OAch dissolved in the glacial acetic acid (0. lmol/40ml) in a three-neck flask were mixed with a solution of titanium tetrabutoxide monomer in butyl-alcohol(l 7ml/20ml) at room temperature and under constantly, vigorous stirring conditions. In most cases, the resultant solution was golden yellow and stable in the air. To this precursor solution, containing Ba, La, Ti in the desired ratio, water was added incrementally for hydrolysis under continuous stirring until sol was formed. After aging for more than 2 hours, sol was transformed to gel at room temperature. If heated during aging, the gel was formed in a shorter time. The wet gel was allowed to dry at 50°C for more than 10 hours. The dried gel was transparent or light yellow. In order to obtain BaTiO3-based nano-crystals, the amorphous dry gel was calcined at 600°C, 700°C, 800°C, 900°C, 1000°C respectively[5]. The ceramic humidity sensor was formed through the cold-pressed, aged, capsulated routes. The dried gels were crushed in an agate mortar and then pressed into discs of ? 1.5 X l.5mm (l.5mm diameter and l.5mm thickness), then held at about 16.5 MPa pressure for 3 min [6]. The disc was sintered at 1350°C and 1400°C for I hour respectively. During the processing, an Ag-Pt electrode was inserted in the sensor [7]. (See the flow chart.)"

Jan 1, 2000

By Tamas Kekesi

Anion exchange in HCl media is considered an efficient alternative to the combination of the conventional purification methods. Anion-exchange distribution functions have been determined for cobalt and the main impurity elements by the technique of batch equilibration. Results were confirmed by spectrophotometric investigations and elution tests. Based on the new and the available distribution functions, combined with the assessment of thermodynamic stability, a procedure of anion exchange separation has been devised to eliminate virtually all the impurities from the cobalt-chloride solution. Separation of copper has been enhanced by the introduction of a preliminary step under reduced conditions. The rest of the impurities are eliminated in a second anion-exchange step applying rinsing and elution stages under oxidized conditions. The optimum parameters of the procedure have been determined according to performance characteristics (purification ratios, yields and volume efficiencies) derived from the analysis of elution curves obtained with laboratory scale ion-exchange columns. Special computer programs have been developed to facilitate thermodynamic simulation, analytical correction and data processing.

Jan 1, 2003

By Na Wang, Chao Du, Hongmin Zhu, Kai Huang, Shuqiang Jiao

"Niobium aluminides were directly synthesized by a sodiothermic reduction process of NbC15 - AlCb which was dispersed into LiCl - KCl - NaCl - CaCb melts. The melt supplied a homogenous reaction medium which was substantially beneficial to the co-reduction of Nb and Al to form niobium aluminides in situ. The reduction was performed at 500°C for 4 hours. The products were analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM). The corresponding results indicated that niobium aluminides powders were successfully synthesized.1. IntroductionNiobium aluminides have received considerable attention as high-temperature structural materials, due to their high melting points, relatively low density, high strength, excellent oxidation and creep resistance [1-4]. Figure 1 shows that there are three intermetallic compounds in the Nb - Al binary [5], which includes Nb3Al (A15 structure, Cr3Si type), Nb2Al (D8b structure, cr-CrFe type) and NbAb (D022 structure, TiAb type). These niobium aluminides have been used in turbine blades or in stationary gas turbines [6-8]. However, despite their attractive features, the ir applications are still limited by the long and costly fabrication process [9, 10].Niobium aluminides were industrially fabricated by the mechanically alloyed process [11-13]. Traditionally, niobium is extracted from Nb2O 5 or K2NbF7 by a metallothermic reduction process while aluminum is produced by the Hall-Heroult process of Ah03 electrolysis. Based on the extraction of Nb and Al, respectively, niobium aluminides is synthesized by a mechanical powder alloying process. The present process for making niobium aluminides requires a set of complicated equipment, has high production cost and time consuming [14, 15].The purpose of this work is to present the simple, economic and direct synthesis of niobium aluminides powders utilizing a sodiothermic reduction from NbC15 - Al Cb dispersed into molten salts."

Jan 1, 2011

By Bo Zhou

During secondary aluminum recovery, complex aluminum scraps are melted and refined often in a rotary melting furnace and the aluminum metal has to pass through a molten salt layer and melt down in a bottom aluminum bath. Previous experimental study and industrial observations have indicated that salt shell formation and re-melting on the metal solids in the early stage plays a critical role in the overall melting process of the scrap. In the present paper, mathematical models are developed to simulate the process of salt shell formation and its re-melting, as well as aluminum melting in the molten melt. Influence of the salt layer properties, the residence time of the metal particles in the salt layer, the particle size, the temperature of bulk melt were investigated. Reasonable agreement with the measurement data was reached. The developed melting model will be used to construct a population balance model of the scrap melting behavior for a rotary melting furnace, taking into account the distributed characteristics of the scrap. Finally, an overall process model based on Computational Fluid Dynamics (CFD) for the rotary furnace will be constructed, coupling with the population balance model for the scrap melting.

Jan 1, 2003

By Guojun Ma

The entrainment of charge materials, evaporation or volatilization of elements and ejection of slag and metal by spitting or the bursting of gas bubbles are mechanisms whereby stainless steel plant dust are generated from the electric arc furnace and refining converter. TCLP and ASTM D 3987-85 tests on dust that was collected from the baghouse filter system of a South African Stainless Steel plant showed that this dust can be considered hazardous according to South African legislation, due to the high degree of Cr (VI) leachability (~13mg/l for TCLP and ~8mg/l for ASTM vs. regulation threshold of 0.05mg/l in drinking water). The dust is therefore considered to be harmful to both the environment and human health, due to its high solubility in water and carcinogenic properties. It should therefore be treated before being stockpiled or land filled. This paper consequently describes an investigation into the formation of Cr(VI)-containing stainless steel plant dust and the stabilisation thereof in a sintering process, whereby the dust was mixed with a silica-rich clay. It is postulated that Cr(VI) form when the (Mg,Fe,Mn,Cr)3O4spinel phase, CaO, Ca(OH)2 and CaF2 (all of which are present in the dust) react. This reaction was found to take place both at ambient and at high temperatures (1100°C). Stabilization of Cr(VI) in the dust could be achieved at an optimum sintering temperature of 1100°C for a 50mass% dust : 50mass% clay mixture. Chromium emission during the sintering process was found to be low, and within environmental limits.

Jan 1, 2006

By Cristiän Vargas, Jaime Simpson, Gerardo Cifuentes

"This paper presents a new process for the precipitation of Sb and Bi present in copper refinery electrolytes in the presence of Pb02 (Chilean Patent No. 45,037). To establish the conditions under which the precipitating compounds form, it was necessary to evaluate the amount of PbCh consumed, antimony extraction efficiency, precipitate stability, reaction kinetics, diffraction analysis and X-ray fluorescence, separation of size, plus observation of the precipitates in the electron microscope. Preliminary tests were carried with synthetic copper refinery electrolyte, and then the final testing was done with electrolytes from Chilean refineries. This process provides a real alternative for the treatment of copper refinery electrolytes for the control of Sb and Bi in solution; it is very simple to operate and is low cost compared with competing processes.Introduction.A high quality copper cathode implies a cathode free of impurities. The electrorefining process seeks to eliminate these impurities from the copper anode (99.5% purity) by its dissolution in an acid electrolyte using chemical and electrochemical reactions. As a result of this process, a cathode (99.99% purity) is obtained. If the concentration of impurities in the electrolyte, from the dissolved anodes, begins to increase; particularly if the antimony concentration in the electrolyte increases up 500 ppm, the formation of floating slimes which are a major cause of contamination of the cathode is favoured. The most important impurities from the point of view of their effect on the quality of the cathode copper, are Ag, As, Sb, Bi, Pb, Se and Te. Silver is necessary for the control of Se and Te. To control all of these impurities, it is necessary to establish different methods or parameters of control in copper electrorefining. These parameters are anode composition, additives, purification of the electrolyte, current density, acidity, etc."

Jan 1, 2012

By L. Béjar-Gómez

The aim of this research work is to study and characterize precipitates in structural microalloyed steel by transmission electron microscopy and analysis by high resolution (HRTEM). Microalloyed steel with titanium was produced by casting in an electrical induction oven of 25 Kg. capacity. Carbon content in steel was less than 0.1 % and titanium content of 0.04%. Steel was processed thermomechanically; reheated to 1250ºC and hot rolled on a laboratory mill to a 13.0 mm thick plate with a finish rolling temperature of 900ºC and thickness reduction of 80%. Analysis by High Resolution Transmission Electron Microscopy (HRTEM) identified precipitates in the steel; type and morphology. Energy Dispersive Spectroscopy (EDS) analysis was applied to obtain the chemical composition of precipitates and the matrix. STEM-EDS analysis was also applied to obtain the element profile of precipitates. The results showed the presence of carbonitride precipitates of titanium, Ti (CN), with a circular morphology and size of 10 nm and less.

Jan 1, 2006

By Keith Rozenburg, Ivar Reimanis, Jesus Chapa

"Experiments in conjunction with finite element analysis (FEA) are used to better predict crack propagation in ductile/brittle graded composites. Cu/W graded composites were fabricated by stacking discrete layers of powders and hot pressing. Crack propagation was studied by loading a notched beam in four point bending and examining the subsequent crack deflection. The notch was placed within a particular composition of material, oriented in a direction perpendicular to the gradient direction. Elastic and plastic mismatch between different constituents in the graded composite induce shifts in the phase angle of loading, thereby causing the crack to deflect. FEA indicates that thermal residual stress has a negligible ""influence on the crack path. The combined FEA and experimental results suggest that elastic mismatch is the single most important material property-related factor in controlling crack deflection.IntroductionMany 'applications would benefit or may even require materials whose performance or functionality must vary spatially. While the concept of functionally graded materials has existed for nearly one hundred years, it is only within the last fifteen years, that research efforts have focused on generic issues in processing, properties and performance of functionally graded materials. This generic research effort has brought together scientists and engineers from traditionally different disciplines to address common issues with graded composites. The current work focuses on issues in structural joining. A wide variety of applications require some type of joining between dissimilar materials. Examples include thermal barrier coatings for turbine engines, wear resistant coatings for tools, ceramic engine parts, and microeiectronic devices, as well as many traditional applications involving metallic welding. The joints may either be discrete, involving a single interface, or they may· be spatially graded in composition. Extensive theoretical and experimental information exists on discrete bimaterial and trimaterial joints, but relatively little exists for graded joints or composites"

Jan 1, 2000

By Lifeng Zhang, Zineb Benouahmane, Yaqiong Li

Experimental oxidation tests at high temperature (1000-1200 °C) on SiC samples have been respectively performed under wet and dry air atmosphere for different holding times. The thickness of thermally grown oxide was experimentally measured by DEKTAK Stylus Profilometry. The results showed that the oxidation rate was increased with temperature and holding time, corresponding to a passive oxidation regime which led to the formation of SiO2 layer. The sessile drop method was employed in order to measure the contact angles between Si and SiC at high temperature. Contact angle can be varied from 39.6° to 75.6° by controlling the atmosphere. The deoxidation of the oxide layer and infiltration of liquid silicon caused a decrease in the contact angle.

Jan 1, 2016

By Xiyun Yang

Magnetite was prepared by hydrogen reduction method. For a conversion to cobalt-modified magnetite, magnetite particles were suspended into a solution containing Co2+ and Fe2+ to precipitate a cobalt ferrite layer on the surface. pH value influences the particle composition directly, the desirable CoFe2O4 is obtained when pH value is 12. The coercivity increases with the increase of cobalt content, cobalt efficiency reaches a maximum value at cobalt content of 2.71wt%. With cobalt modification, magnetite particles have similar lattice constant and squareness ratio to that without cobalt modification. TEM and XPS analyses indicate that acicular morphology is retained during the coating process, the epitaxial growth layer consists of CoFe2O4and 0.3Co2O3CoFe2O4 at cobalt content of 2.71wt% and 5.03wt%, respectively.

Jan 1, 2006

By Nobuaki Sato

The electrical conductivity, k, of pure and sodium doped sulfur melts was measured with and without ultrasonic waves at temperatures ranging from 140 to 340° C by the two probe method using an ultra high resistance meter. The II: value of the pure sulfur melt with irradiation jumped at around 170°C by an order of 102 after which it monotonically increased from 10-5 to 10-4 (omega) 1cm-4 with an increase of the temperature. The addition of the sodium metal to the sulfur melt was found to cause a larger jumping in the II: value. The II: value increased with the increase of Na proportion in the melt. For a 10 mol% Na doped sulfur melt it was as high as max. ~30 (omega) 1cm-1 above 180°C under the irradiation of ultrasonics.

Jan 1, 2003

By Charles I. Richman

Aquispirillum magnetotacticum (AM) is gram-negative hetrotrophic bacteria that belongs to a class ,of magnetotactic bacteria that have an ecological niche in marine marches and fresh water swamp sediments. Thiobacillus Ferrooxidans (TF) is a Gram-negative, acidophillic chemoliths that may have similar chemical conditions within the cytoplasmic membrane as Aquaspirillum M. to support growth of Magnetosomes. Magnetosomes are cellular bodies that accumulate under slightly aerobic conditions. Magnetotactic motion occurs in an external magnetic field and depends on the medium viscosity. The Atomic Force Microscope equipped with a magnetic tip shows the presence of Magnetosomes in these bacteria strains. The size, shape of magnetosomes in AM and TF strains are characterized.

Jan 1, 1998

By E. J. Peuraniemi

Recently commissioned Kennecott-Outokumpu flash converting was developed to replace the approved but environmentally outdated Peirce-Smith -converting to satisfy the globally tightening emission regulations. In the present study, dust formation and reaction mechanisms of two copper mattes with different experimental parameters were studied in lean suspension conditions. Both mattes had very high copper content of approximately 75 wt% and low iron content of 4.5 wt% and 1.2 wt% Fe. A laboratory scale, vertical laminar-flow furnace with a low feeding rate was used to simulate the phenomena taking place in the reaction shaft of a flash converter. Experimental conditions included temperature of 1300 °C with reaction gas oxygen contents of 20 vol%, 50 vol%, and 75 vol%. In the experiments, sieved particle fractions were fed to the furnace and sampled after short reaction time intervals by quenching them into a water film. Collected particles were analysed chemically for their main elements to define their removal rates. Also, optical and scanning electron microscopy with EDS-analyser were applied to determine phenomena occurring during reactions. Kinetics of oxidation as well as ignition of particles are discussed. Changes in particle morphology, size, and composition are reviewed to describe dust formation and reaction mechanisms.

Jan 1, 1999

By Renato G. Bautista

"The development of processing methods for the preparation .of three electronic materials with rare-earth components is discussed. The resulting processing innovations are the results of a search for an economically competitive pilot scale or industrial production flowsheet without compromising the required properties of the final products. The three cases highlighted in this presentation are: 1) The preparation of high energy (Pr-Nd-Ce)FeB magnets for MRI application from a mixed-rare-earth oxide with a narrow range of composition directly prepared from the solvent extraction circuit of bastnaesite ore. 2) The kg production of the giant magnetocaloric effect Gds(SixGe1-x)4 magnetic refrigerant materials from commercial grade gadolinium metal (95 to 98 at. % pure) instead of high purity gadolinium metal (99.8 at. %); and 3). An industrial chemical synthesis flowsheet for the production of the superconductor precursor of YBa2Cu3O7.INTRODUCTIONIn the laboratory discovery stage, the synthesis of a new material is carried out using very high purity components, usually the highest purity available. As the new material is studied and characterized, the effectiveness of its desirable properties becomes better defined and understood. The evaluation of the effectiveness of the .property over the range of a given parameter and other interactions are further studied. Once it's potential application becomes clear, a practical and economical processing method need to be developed. The successful material processing flow sheet does not necessarily have to be a scale up of the laboratory procedure. At this stage, substitution of starting components and with lower purity materials is considered as the economics of the processing becomes a major issue. In addition, other approach to it's synthesis"

Jan 1, 2000

By Maria Cristina Ruiz

The removal of iron from the leaching circuits is a common problem in the hydrometallurgical processing of non ferrous metals. Among the currently available processes, hematite precipitation is the most recommendable from an environmental point of view. This paper is concerned with the batch precipitation of hematite from ferrous sulfate solutions. One of the main objectives of the study was to determine the effect of the experimental conditions on the extent of iron precipitation as well as the purity and the particle size distribution of the precipitates. The main variables studied were temperature (180 to 220 ºC), concentration of sulfuric acid (1 to 10 gpl), initial iron concentration (1 to 15 gpl) and partial pressure of oxygen (3 to 7 atm). The results showed that increasing the oxygen partial pressure from 3 to 7 atm produced a very small increase on the rate of hematite precipitation indicating that a large partial pressure of oxygen is not needed for an effective ferrous to ferric oxidation. An increase in the temperature produced finer precipitates with lower sulfur contents. On the other hand, an increase in sulfuric acid concentration and initial iron concentration produced precipitates with larger particle sizes and higher sulfur contents.

Jan 1, 2006

By Hiroaki Nakano, Kenji Hara, Shunsuke Kawano, Takeshi Ohgai, Michiaki Ikeda, Hisaaki Fukushima, Shinji Yamashita, Tetsuya Akiyama, Hisayuki Kaku

"Ni-Fe alloys have an inverse magnetostrictive effect (Villari effect) in which its permeability varies according to the ·applied strain. This alloy film has a potential for application as force sensors such as torque sensors, tension sensors and so on. Electrodeposition is promising as a technique for preparing Ni-Fe alloy film because of its convenience and economy. In this paper, the effects of electrolysis conditions on the magnetic properties of electrodeposited Ni-Fe alloy films were investigated. Hysteresis loops of Ni-Fe alloy films on copper substrates from sulfate bath were measured by a vibrating sample magnetometer (VSM). The films of low coercivity, which were preferred when used as a force sensor were obtained by introducing certain additives to the sulfate type bath.INTRODUCTIONNi-Fe alloys show an inverse magnetostrictive effect (Villari effect) that their permeability varies depending on the applied strain. The films of this alloy have a potential for application as force sensors such as torque sensors, tension sensors and so on. The authors et al. tried to prepare Ni-Fe alloy films using the sputtering technique, and produced a prototype of Ni-Fe alloy torque sensor [I]. The sensitivity was higher in the torque sensor thus produced than the strain gauge type one, and this torque sensor enables non-contacted detection. It showed excellent durability and reliability. However, the formation of Ni-Fe alloys by sputtering requires higher costs and brought an another problem that the shape of the substrate on which the film was formed was considerably limited. This causes a hindrance to the wide-range application of the force sensors. Electrodeposition is promising as the technique for preparing Ni-Fe alloy films because of its convenience and economy. In this paper, the effects of the conditions of electrodeposition on the magnetic properties of Ni-Fe alloy films were studied."

Jan 1, 2000

By C. J. Beyke

Slags and/or mattes from three secondary lead producers were studied as part of an effort to develop treatment methods for these lead-bearing residues. Each company used a somewhat different production process. Company A used a reverberatory furnace followed by a blast furnace. Company B used only a blast furnace. Company C used both a reverberatory and a blast furnace, and the scrap material was desulfurized with sodium carbonate prior to smelting. The slag matrix produced from sulfur-bearing scrap consisted mainly of iron-calcium silicates; the slag from desulfurized material was similar, but also contained sodium. In all the slags most lead was present in metallic form, often alloyed with tin, antimony, arsenic, and/or iron. Slag from Company B contained the most alloying elements, often as discrete subparticles within the lead droplets. Mattes were produced at Companies A and B; predominant phases were pyrrhotite and magnetite, while lead was present in metallic form and as galena.

Jan 1, 1995

By Satoshi Yamashita, Noboru Masuko

"Newly prepared bipolar membrane is promising to become a key material of an electrolyser for a production process of strong reducing solvent. This research is basic research for using bipolar membranes as electrolysers of reducing agents, Cr(II), TI(III) and V (II) on the laboratory scale. In this report, a bipolar membrane was tried with an electrolyser, reducing chromic chloride to chromous chloride. An analysis of mass balance demonstrates advantages of it over the former electrolyser equipped with an anion and/or. cation exchange membrane. The effects of current density and concentration of Cr(lll) on the reduction rate of Cr(II) and the current efficiency were examined No deterioration of the bipolar membrane resulted from the electrolytic reduction of Cr(III). IntroductionRecently, bipolar membrane that was the development subject for a long time in the industry of ion exchange membranes has met the stage of the practical application at last [l]. The expectation of the application to the hydrometallurgy field increases. We took up the manufacturing of the strong reducibility solvent as part of the application of bipolar membrane to hydrometallurgy technology. This laboratory has much experience in the electrolytic reduction of Cr (II) aqueous .solution such as chromous sulfateusing bipolar membrane were compared in theory to chromous chloride aqueous solution manufacturing of the strong reducibility solvent. The advantage of applying bipolar membrane by substituting ion exchange membrane is described, and the experimental result is reported."

Jan 1, 2000

By Hector M. Lizama

A new technology, known as the HydroZinc? process, is described for the recovery of zinc from sulphide ores that includes heap leaching, neutralization, solvent extraction and electrowinning. Unit operations were scaled up from bench-scale to a 1-t/d zinc cathode demonstration plant. Bench-scale studies defined the process chemistry and a process flowsheet. Column tests were used to design full-scale heaps for zinc bioleaching, and mini-pilot equipment was used to design a solvent extraction circuit. The characteristics of the process required development of a bleed circuit for water and impurities. The complete integrated process was tested on a demonstration plant scale for two years, with about 10 000 t of zinc sulphide ore being bioleached in two 6-m-tall test heaps. In addition to 1 t/d of zinc cathode, iron hydroxide and gypsum residues were produced. The process also generated a small effluent bleed. Over the course of the two-year demonstration test, a number of technical hurdles were overcome and several improvements were made. Some of the more significant ones are presented along with process descriptions and experimental and demonstration plant data. Some engineering aspects and economic evaluations of the new process are also discussed.

Jan 1, 2003