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By Cesimiro Fabian

The crystallite size of copper electrodeposits was determined by X-Ray powder diffraction analysis using a General Area Detector Diffraction Solution (GADDS) diffractometer. Crystallite size was calculated for copper thin films which were deposited on a 316 stainless steel rotating cylinder electrode (RCE) in the presence and absence of additive ?A?. The crystallite size was calculated from a corrected full width at half maximum (FWHM) of the [110] peak profile using the Scherrer equation. The test of significant difference on crystallite size was derived using Kruskal-Wallis method. It was found that in the absence of the additive the median crystallite size was 426, which decreased to 364 in the presence of the additive. As the additive degraded, the crystallite size increased to a size similar to that observed in the absence of additive.

Jan 1, 2003

By E. Allaine

Carbochlorination kinetics of pure MoO3, Nb2O5, Ta2O5 and V2O5, by Cl2+CO+N2 gas mixtures was investigated between 380 and 1000 °C. Standard free energy of carhochlorination reactions and phase stability diagrams of these refractory metal compounds were calculated. The influence of total gas flow rate, temperature, reactants partial pressures on the reactivity of these oxides were investigated. The apparent activation energies were found to be about 83, 75, 110 and 100 kJ/mole below 650°C for MoO3, Nb2O5, Ta2O5 and V2O5, respectively. Above this temperature, the Arrhenius plots exhibit a rate anomaly attributed to thermal decomposition of COCl2 and/or structural changes of these refractory metal oxides. The apparent reaction order of carbochlorination of these oxides with respect to Cl2+CO was determined. For these refractory metal oxides, the reaction rate was maximum for a Cl2/CO ratio of about 1 in the chlorinating gas mixture. Results of carbochlorination of these oxides are compared and discussed.

Jan 1, 1995

By Y. Fukunaka, M. Niinae, E. Kusaka, T. Kuzuya, R. Ishii

"Samarium oxalattr particles was precipitated in oxalic acid aqueous solution from samarium-loaded D2EHPA solution emulsified with a conventional impeller. The calculated fractional precipitation of samarium oxalate was reasonably compared with the value determined by chemical analysis. Morphological variation of oxalate precipitate particles was then examined with H2C2O4 concentration in aqueous solution, Sm(III) and D2EHPA concentrations in organic phase. The needle-like precipitate was identified as Sm2(C2O4)3 10H2O by XRD. Precipitates obtained at higher H2C2O4· or Sm(III) concentration greatly decreased the length of major axis of precipitate, while those at higher D2EHPA concentration increased it. The oxalate was further precipitated under ultrasonic irradiation. However, the morphological variation caused by theses processing variables was not so evident under ultrasonic irradiation as in an impeller or shaking mixer.IntroductionThe materials processing of the rare earth elements must be reviewed from the scope of industrial ecology, since they have the potential applications of magnetic materials as well as secondary battery in developing programs of the electric vehicle. The technological trend to develop the electric vehicle may greatly influence the concept of materials processing, since the global· environmental problem must accommodate with the sustainable development for mankind. The recycle design must be a key issue in the materials science and engineering.Solvent extraction provides a unique separation technology -in this sense. Doyle (1)(2) reported the integrating solvent extraction with processing of advanced ceramic materials, whose chemical composition and microstructure must be precisely controlled. In her paper, the higher productivity inherent to the present process superior to hydrolyzing metal alkoxides was emphasized. Oxalic acid has been used as precipitant for rare earth purification process, since rare earth oxalate has a very small solubility in water and can be easily decomposed to oxide. It is thus suitable for precipitation stripping agent in cationic exchange type extracting system (i.e. D2EHPA, VA-10, PC-88A and so on)."

Jan 1, 2000

By C. E. M. Meskers, U. Boin

"The increasing use of coated magnesium in consumer products results in creation of coated Mg scrap during product manufacture and after End-of-Life product treatment. Currently this material is generally not recycled, leaving a material resource unused. Closure of the magnesium cycle in a sustainable manner is necessary. In order to do so, the effect of coatings on the recycling process has to be quantified, predicted and minimized. For this purpose metrics have been developed, based on first principles supported by detailed understanding of the recycling process. The developed 3D metric enables quantitative assessment of the recyclability and links coating design, product design and recycling to each other in a visual manner. The parameters that form the metric can be measured and predicted, hence an engineering basis for Design for Sustainability of coated magnesium is provided.IntroductionEvery product progresses through the four phases of the product life cycle depicted by figure 1. In each phase residues are created. Their amount and composition is largely determined by the complex material combinations created/invented during product design in the manufacture phase. Compared to the ideal cycle the magnesium cycle is far from closed (fig. 2). Most noticeable is absence of the link between the EoL phase and raw materials production. A closed cycle only exists for class 1 scrap, which goes from the product manufacture phase directly to production from industrial material and returns to the manufacture phase as magnesium alloys. The four problematic streams are marked by ???. Coated semi-products are present in two of the four residues, namely in rejects and collected scrap. When these semi-products are recycled the amount and composition of the dross and salt slag residue is affected as well.During product design selection of the coating takes place, fixing the coating character¬istics and properties from this moment on for the rest of its life cycle. The choices made in the manufacturing phase are therefore critically linked to the recyclability of coated semi-products as well as the sustainability of the magnesium cycle as a whole. Sustainable closed life cycles, in which the quality of materials is preserved and residue creation and resource depletion are minimized, can be attained by selecting the appropriate alternative during product design. To realize this the effect of design choices on the life cycle and more specific the recycling process has to be known and quantified."

Jan 1, 2008

By A. Alvarez

In this work, mesophilic and thermophilic cultures have been used in the presence of silver as a catalyst. Chalcopyrite and byproducts of bioleaching were characterized in order to: a) obtain information about the kinetics control of the process, and b) explain the different behaviour observed during the mineral attack. With thermophilic microorganisms (68°C and Norris medium as nutrient) the reaction stopped at approximately 65% copper extraction, with and without Ag ion addition as a catalyst. The remaining chalcopyrite appears surrounded by hydronium jarosite (with ammonium ion in substitution in the "alkaline site"), goethite and elemental sulphur. With mesophilic cultures (35°C and 9K medium as nutrient) the reaction stopped at approximately 25% copper extraction (without Ag) and approximately. 85% extraction (with Ag). In both cases, the remaining chalcopyrite was surrounded by agglomerates of ammonium jarosite (with hydronium ion substitution in the "alkaline site") and some iron oxides and/or hydroxides.

Jan 1, 1999

By Du Sichen

The present paper presents the modeling of gas-solid reactions in the case of the decomposition of CaCO3, describing the reaction kinetics on the basis of heat-transfer concepts which could be compared with thermogravimetric results. In the case of solid-solid reactions, the present paper describes the model developed for describing solid-solid reactions from dynamic X-ray diffraction technique, developed by the present team. The model has been successful in explaining the formation of spinel from MgO and Al2O3.

Jan 1, 2006

By Karel Verscheure

Reliable furnace cooling technology is a domain of increasing concern to the pyrometallurgical industry as it can significantly increase process intensities, productivity and campaign times of furnaces. Although there are many advantages in using cooling systems, they also impose a variety of problems mainly related to safety, heat losses and sustainability of the operations. The choice of cooling system is hence a matter of trade-offs and differs for every metallurgical application. This paper gives a review of different cooling designs used in the ferrous, non-ferrous and alloying industries. Additionally, the paper systematically reviews aspects of materials selection, manufacturing, installation, water quality and furnace monitoring when using water cooled refractories.

Jan 1, 2006

By Ximena Massone

Chile is the most important copper producer in the world and the mining sector plays a key value in its economy. However, at present the country does not have a satisfactory set of regulations about closure and restoration of mining operations. In our country many mining operations will, in the near future, shut down their activities, therefore, it is of utmost importance to elaborate and enforce a set of regulations to prevent risks and to protect the environment. The present study is focused on reviewing and analyzing the existing national regulations about the closure of mining operations and preparing a comparative analysis with other international regulations of countries with mining experience. The final results of the study will be a legal proposal to regulate the closure of mining operations in Chile, aiming at minimizing the potential environmental adverse impact, internalizing the social costs by the relevant operators and defining all aspects of liability for the environmental damage.

Jan 1, 1999

HW Process Technologies, Inc. (HWPT) has developed a patented membrane-based ion fractionation system, which specifically separates copper from gold and silver species in a cyanide matrix. This Engineered Membrane Separation (EMS?) system was pilot demonstrated on the 82,000 liters of pregnant leach solution' (PLS) generated from tailings, via thin layer leaching, at a mine site in Durango State, Mexico. The EMS? recovered ~90% of the gold-silver cyano-complex to a 90% volume permeate (based upon an EMS? feed stream of 100% volume) while rejecting -90% of the copper cyano-complex to a \0% (by volume) concentrate. The EMS? technology combines pore-size specific electro-statically charged membranes with engineered materials of construction and application-specific operational design that reject multi-valent, ionically charged species to the concentrate and transmit mono-valent species through the membrane to the permeate. The 850 ppm Cu PLS contained approximately 0.8 gil free NaCN with, the copper cyano-omplex principally in the CU(CN)3 and CU(CN)4 forms. The gold grade of the PLS was -2 ppm Au. The ~LS calcium concentration at -700 ppm Ca was reduced to ISO ppm.Ca (± 50 ppm) by sodium cycle ion exchange pre-treatrnent prior to EMS? processing.

Jan 1, 1998

By E. R. Vance, D. R. M. Brew

"Historically, Ordinary Portland cement has been the preferred medium to immobilise arsenic. However, arsenic in cement gives rise to calcium-arsenic phases and their known decomposition to calcium carbonate and arsenic trioxide via atmospheric carbonation raises serious questions about the long-term suitability of cement for arsenic immobilisation. Alternative matrices such as low-temperature ceramics (LTCs) potentially offer superior resistance towards carbonation owing to the absence of calcium. Consequently, the potential for arsenic immobilisation using LTCs has been investigated. Both AsIII and AsV have been incorporated and samples assessed according to a standard leaching protocol. AsIII persists in the porewater of alkali-bonded LTCs as sodium arsenite rendering them unsuitable for immobilisation. Thermal treatment of these LTCs to consolidate the microstructure and reduce open porosity resulted in sodium-rich cryptocrystalline matrices that leached arsenic and sodium readily. The omission of sodium in acid-bonded LTC formulations resulted in leach data that were close to the target value of 5 µg/ml in Toxicity Characterisation Leaching Protocol tests.IntroductionArsenic is a carcinogenic substance and its adverse effects of on humans, flora and fauna have been well documented [1-5]. As a consequence, many papers have been written on the prospective handling of arsenic-bearing waste. These can largely be divided into: (a) cleanup of arsenic-contaminated water using bacteria, precipitation, and/or UV irradiation to generate arsenic-rich sludges for subsequent immobilisation; (b) cleanup of arsenic-contaminated soil via chemical extraction for immobilisation of the As concentrate; and (c) immobilisation of industrial waste contaminated with As."

Jan 1, 2008

By Frame Ritzert, Dennis Keller, Vijay Vasudevan, David Arenas

"An investigation was conducted to describe topologically close packed (TCP) phase instability as' a function of composition in the advanced ·Ni-base superalloy Rene N6. TCP phases are detrimental to overfill high-temperature performance of Ni-base superalloys because of their brittle nature and because they deplete the Ni-rich matrix of potent solid solution strengthening elements. Thirty-four variations of polycrystalline .Rene N6 determined from a design-of-experiments approach were cast and homogenized at 13 l5°C for 80 hours followed by exposure at 1093°C for 400 hours to promote TCP formation. The alloys had the following composition ranges in atomic percent: cobalt 10.61 to 16.73, Mo 0.32 to 1.34%, W 1.85 to 2.52%, Re 1.80 to 2.11%, Ta 2.36 to 3.02%, Al 11.90 to 14.75%, and Cr 3.57 to 6.23%. Physical and chemical characteristics of all microstructures obtained were described using various analytical techniques. From these observations, a mathematical description of TCP occurrence (s and P phase) was generated for polycrystalline Rene N6.IntroductionNi-base superalloy single crystals represent the state-of-the-art for turbine engine airfoil application as they offer the best balance of properties to allow for the high operating temperatures required: for efficient engine operation.1 Current trends in alloy design take advantage of improved creep rupture strength with the addition .of higher levels of refractory elements. 2 In .particular, the addition of significantly higher levels of Re in third generation superalloys is key for both microstructural stability and creep rupture strength. 3 While the presence of the refractories is thought to provide strength benefits from solid solution hardening, a tendency for alloy instability in the form of topologically-close-packed (TCP) phases or secondary reaction· zone (SRZ) ·phenomena accompanies the high refractory content. 3 The formation of these phases in sufficient amount is detrimental to the overall high temperature performance of Ni-base superalloys because of their brittle nature and because they deplete the Ni-rich matrix of potent solid solution strengthening elements.4 The tendency for a particular composition to form TCP may not be immediately known since the precipitation of TCP phases in Ni-base superalloys is nucleation controlled, thereby requiring long times at elevated temperatures to precipitate. 5 They preferentially nucleate along the octahedral planes of the Ni-base superalloys, usually in areas of refractory metal enrichment at grain boundaries or inside dendrites.5-6 In Rene N6, two closely related TCP phases, a and P, have been observed.2"

Jan 1, 1998

Mount Isa Mines Limited (MIM) and the Commonwealth Scientific and Industrial Research Organization (CSIRO) have, over the past 15 years, jointly developed the Isasmelt process. This process is based on the use of the Sirosmelt top-entry, submerged combustion lance, developed by the CSIRO in 1973. While the Isasmelt technology was first applied to lead smelting, it has more recently been adapted to smelt copper concentrate. A 15 t/h demonstration Copper Isasmelt plant was commissioned in MIM's Mount Isa copper smelter in April 1987. The success of the Copper Isasmelt demonstration plant, which smelted over 532,000 metric tons of copper concentrate, has led to the construction of two full-scale furnaces: a 104 t/h furnace in the Mount Isa copper smelter, and a 585,000 t/y (650,000 short t/y) furnace at the Cyprus Miami Mining Corporation smelter at Miami, Arizona. The commissioning of these furnaces commenced in August and June 1992, respectively. The MIM Copper Isasmelt furnace will raise the Mount Isa copper smelter's capacity to 265,000 t/y of copper. The plant includes several innovative features, including: Andritz pressure filters, a rotary holding furnace, and an Ahlstrom flux-flow boiler.

Jan 1, 1993

By George Owusu

A study has been carried out on the use of solvent extraction, instead of the traditional zinc dust cementation process, to remove copper from concentrated zinc sulphate leach solutions. In a series of experiments using plant solution containing 1.9 g/L Cu, 2 g/L Fe, 173 g/L Zn, 7.9 g/L H,SO,, 0.25 g/L Cd, 15 mg/L Co etc. and LIX 622 in SX-1, up to about 97-98 % of copper present in the zinc sulphate leach solution was extracted with negligible co-extractions of zinc, iron, cadmium, cobalt, etc. pH modification was not required for this reagent. The copper loaded organic was almost completely stripped using 150 g/L sulphuric acid. Investigations into the effect of any possible organiclextractant contamination on zinc electrowinning showed (if any) little effect on current efficiency if the organic contamination is less than 45 ppm; current efficiencies of 95-97 % were obtained. At organic contaminations higher than 45 ppm, the current efficiency dropped to about 92- 94 %. Visually, the organic-contaminated cathode sheets had rough surface morphology, becoming more intense with increasing organic concentration, compared to the non-contaminated cathode sheets.

Jan 1, 1998

By R. Parada

A real-time dynamic simulation model has been developed to characterise the flash furnace operation at the Chagres smelter. This model permits the operators to plan the process to meet the Peirce Smith converters' schedules and feed the acid plant with gases that satisfy its best operating efficiency range. Essential control parameters for the furnace (process air enrichment, oxygen coefficient and supplementary heat) are calculated to satisfy process targets such as matte grade, slag silica and matte/slag temperatures. These calculations are carried out with a real-time simulation. Flash furnace control and operational stability permits setting up control strategies that streamline the flow of copper to converters and of sulphur to the acid plant.

Jan 1, 1999

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

"Lead-zinc mineralization is distributed in Egypt along the Red Sea coast between El Qusier and Ras Banas. A representative sample from Um Gheig was collected and ground to -60 mesh for the mineralogical study. It contains hemimorphite (Zn2SiO4.H2O), sphalerite (ZnS), galena (PbS), calcite (CaCO3) and dolomite (CaMg(CO3)2) beside the gangue minerals gypsum (CaSO4.2H2O) and hematite (Fe2O3). Cadmium seems to be incorporated in the crystal structure of the zinc-lead minerals. The chemical analysis of Um-Gheig representative sample revealed that, it contains 16% zinc combined with 0.1% cadmium, 2.3% lead and 0.1% boron beside other elements.Pug and agitation leaching were performed on samples ground to -200 mesh to achieve the maximum dissolution efficiency of cadmium with respect to other elements. Cadmium leaching efficiency reached 90% by using 40% H2SO4 at S/L ratio 1/2 and stirring time 2 hours at 80o C. Cadmium was then separated as yellow precipitate of CdS from the sulfate leach liquor containing 0.9 g/l Cd, 145 g/l Zn, 0.15 g/l B and 0.01 g/l Pb. Separation of cadmium was carried out by direct precipitation using Na2S as well as H2S. The recovery of 94% cadmium free of zinc was achieved.IntroductionLead-zinc ores occur in Egypt in a few localities distributed along the Red Sea coast between El Qusier and Ras Banas. Um-Gheig Pb-Zn ore is a replacement deposit in limestone and calcareous sandstone in the basal series of the Middle Miocene rocks. The reserve of the ore deposits has been estimated by Soviet and German Experts to be about 900,000 Ton, Bishai [1]. As has been mentioned, zinc is a common element and cadmium is comparatively rare in almost zinc minerals. It was estimated that zinc is 200 times as abundant as cadmium. According to Bodas [2] about 2.1% of cadmium was carried by the Zn mineral hemimorphite (15.3% Zn) in Thailand. Also, Onal et al., [3] found that 164 g/t Cd was carried by Pb–Zn ore sample containing 10.17% Pb and 10.98% Zn from Aladag in Turkey. Cadmium metal has gained great importance due to its wide applications in civil and navy purposes as well as in nuclear field. It is characterized by its ability to absorb thermal neutrons during the chain reaction inside the nuclear reactors. It is also used in the manufacture of sheets which directed the chain reactions [4]."

Jan 1, 2008

By David Ellis

The next generation of Reusable Launch Vehicle (RLV) will utilize regeneratively cooled combustion chamber liners in the engines. The current design calls for using a new Cu-8 at. % Cr-4 at. % Nb (Cu-8 Cr-4 Nb) alloy for the liners. Work is ongoing to characterize the thermophysical and mechanical properties of the alloy from - 253 to 800°C, the temperature range to which the alloy will be subjected during service. The alloy has been commercially produced in quantity for NASA. The powder size has been characterized and the microstructure examined. The powder was extruded into bar using a commercial extrusion press. In addition, samples have been hot isostatically pressed (HIPed) at NASA Glenn Research Center. Both processing methods produced fully consolidated material. Transmission electron microscopy (TEM) revealed highly faulted Cr2Nb and some elemental precipitates. Cryogenic tensile testing showed the extruded specimens had significantly higher strengths than NARloy-Z (Cu-3 wt % Ag-0.5 wt % Zr) even after being subjected to a simulated braze cycle. The Young's moduli (Cu-8 Cr-4 Nb) were lower than NARloy-Z. The lower moduli is highly beneficial for reducing thermally induced stresses in rocket engine combustion chamber liners and similar applications.

Jan 1, 1999

By J. M. Tourre

1995 have seen a continuation of a positive trend in the Rare Earth industry The availability of a greater diversity of Raw Material has brought additional flexibility to the Producers permitting better economics China remains the major raw material source; Chinese concentrate producers have increased capacity in 1995 (Baotou, Sichuan, etc) China's role in the Rare Earth industry will continue to evolve; the acquisition of a majority equity position by San Huan/CNNC will have a significant impact on both the Rare Earth and Magnet markets Chinese producers are increasing the quality of their products and realize their true values Chinese market, itself, is also changing as the internal needs for separated rare earth's grow Already already producer of Lamps, Loudspeakers, Magnets, and TV tubes, China is in an unique position where the potential of its internal market might be more promising than the prospects outside China 1995 has also seen the application market become more diverse and complex. There are new applications growing at a very strong pace (such as battery alloy), applications that are now penetrating their target markets with significantly increased growth rates (such as bonded NdFeB), and some applications that became more complex requiring much more sophisticated products (such as catalysis). Rare Earth producers have to spend significant ressources in order to monitor the market trends in order to predict the demand and then adjust their raw material mix. Even though there is a greater diversity of raw material available, there is still some Rare Earth elements that are in excess, while other are just in balance. As a consequence rare earth producers invest heavily in R&D in order to develop new applications for these excess elements.

Jan 1, 1997

By A. V. Tarasov, S. D. Klushin

493 The most common method for minimizing the copper content of residual slag in the process of autogenous smelting of sulfide raw materials is treatment of molten slag in an electric furnace, with optional addition of solid reducing agents, such as coke, and/or sulfiding agents such as pyrite. A drawback of this technique is the fact that the final slag produced still contains 0.5% or more Cu. We have tested a method for treating molten slag obtained as a result of autogenous smelting by a gaseous mixture of sulfur dioxide and methane at a ratio of. SC:SO2 = 0.75 :1.0 in the presence of oxygen. Interaction reaction within the SO2-O2-CRi system proceeded at a high rate at 1373 to 1573 K to form reducing and sulfiding agents: H2S, S, COS, CO, CO2, H2, H2O. The gas mixture requirement was about 100 to 150 Nm3 per 1 tonne of slag. A decrease in the ferric iron concentration (Fe3+) from 10-15% down to 2-3% resulted in lower solubility of copper in slag, and agitation of the melt with gas stream accelerated. the separation of the sulfide phase and slag. Removal of copper from slag was performed in a pilot unit within the second V anyukov furnace zone where slag arrived with a copper content of 0.8-1.3%. The temperature of molten slag was maintained within 1523 to 1573 K. The copper content of the final slag was at a level of0.12 to 0.14%. The matte sent to converting was a mixture of bottom matte from the smelting zone and the slag treatment zone. It had a copper content of about 50 to 55%. Process gases from both furnace zones were combined and sent to the acid plant for sulfur recovery. This process was offered for commercial use at two copper smelters in Russia and CIS.

Jan 1, 2000

By David J. Howard, Christine Broadbridge, David C. Paine

"High pressure vapor/solid reactions offer an opportunity for novel synthesis and processing of thin film materials and structures for electronic, optical, and magnetic applications. In this paper we review the use of two high pressure techniques that operate from 25 to 1000 atm (2.5 to 100 MPa) to fabricate thin film oxide structures from Si1-xGex deposited on Si wafers. High pressure synthesis enables temperature-independent control of reaction rates in the oxidation of this multicomponent semiconductor system and hence offers the opportunity to form thennodynamically metastable Si1-xGex<h from the alloy. The thermodynamics of the Si-Ge-0 system are reviewed and a method is described that utilizes selective chemical reduction (via H2 gas) of Si1-xGcx<h to form Ge precipitates in an SiO2 matrix. IntroductionAlloys of Si1-xGex grown epitaxially on Si substrates by chemical vapor deposition (CYD) and molecular beam epitaxy (MBE) have been used to create high performance microelectronic devices1. These devices show improved performance over conventional Si technology because they exploit the Si/Si 1-xGex band-gap discontinuity and take advantage of higher hole mobilities in the Ge containing alloys. While a range of devices based on heteroepitaxial systems have been demonstrated, the Si1_xGex alloys are of particular interest because they are most closely compatable with standard Si device processing. One disadvantage of Si-based materials systems is that they are not typically useful emitters of light. This is important since the use of light (rather than electrons) for transmitting and processing signals into, out of, and within Si-based microelectronics would represent a major technological advance in microelectronics-based communication and computer technologies. Nevertheless, through the use of innovative processing techniques it may be possible to use the Si1_xGex/Si heteroepitaxial system in integrated microelectronic/light-wave technologies."

Jan 1, 1994

By M. Potesser

After the primary or secondary lead production the bullion lead is remelted and charged into a vessel with following refining process. The removing of arsenic, antimony and tin takes place by salt slags or oxidizing gases like air or pure oxygen. Due to the increasing lead price, Messer Austria GmbH in cooperation with the institute of Nonferrous Metallurgy at the University of Leoben have developed a new process named OXIPOT for the refining of tin, arsenic and antimony. The OXIPOT process is in principle based on purging technology with a ceramic or steel purging device. This leads to an increased retention time of the refining products due to the deeper bath level and an optimized specific reaction volume concerning the bubble size. This paper describes the process, pilot plant, and thermodynamic calculations for the optimization concerning the selectivity of element removal.

Jan 1, 2008