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By Biao Zhou, Qian Li, Kuo-Chih Chou, Yi-Long Liang, Jie-Yu Zhang, Qun Luo

"In this work, the phase transformational behaviors and microstructural characteristics of 60Si2CrVAT spring steel were systematically investigated as a function of applied cooling rates in the range of 0.l-10°C/s. A quenching deformation dilatometer was used to austenize and quench. The dilatometric curves between length changes and temperature of samples suggest three characteristic stages could be identified as different ranges of cooling rates, which meets well with metallographic examination and the measured hardness results. As the cooling rate increases, the structure transformed from pearlite, granular bainite to finally martensite. The F + P and B zones are completely overlapping in continuous cooling transformation (CCI) curve, which indicates that this steel is difficult to become single bainite and shows good hardenability.IntroductionThe 60Si2CrVAT, a high-carbon low ally super-high strength steel developed from the ?OCT 60C2XFA and 60Si2MnA, is often used for coil spring of heavy vehicles and high-speed railway by hot deformation or cold deformation [1-3]. The addition of Si improves relaxation resistance significantly, through the refinement of tempered carbides as the result of the retardation of E -carbide conversion to cementite during tempering. Due to its deleterious effects on decarburization and toughness, the maxinJum content of Si has limited to 1.5 or 2.0% [4-5]. Additionally, V and Cr can improve sag resistance due to the precipitation of fine carbonitrides during hot rolling [6-7]. To best of our knowledge, the strengthening by precipitation of alloy carbides of Cr and V often referred to secondary hardening [8]."

Jan 1, 2013

By Leah Penner, Thomas J. Ruth, Paul Schaffer, François Benard, Edouard Asselin, Stefan K. Zeisler, Thomas J. Morley

"This paper details the electrodeposition of metallic molybdenum from an aqueous, acetateelectrolyte containing molybdate ions. The deposition is carried out in a highly concentrated (up to I 0 M) acetate bath in the presence of a very low concentration of bone glue (60 µg/L). The molybdenum metal deposits are up to 20 µm thick and adherent. The deposits were characterized by XRD and XPS analysis. The deposition process is very inefficient, as up to 99% of the current is used to generate hydrogen during electrolysis. The effect of acetate concentration, pH, additives and current on the deposition efficiency and physical properties of the molybdenum deposit were investigated and optimized to obtain smooth, adherent coatings.IntroductionMolybdenum has increased thermal and wear resistance properties that are often utilized in material coatings [I]. These coatings are most often manufactured by sintering, pressing or spraying molybdenum powder at elevated temperatures, as a substitute method for standard metallurgical practices, such as electroplating [2, 3]. The lack of reports describing molybdenum deposition is most likely due to the highly oxophilic nature of molybdenum and the stability of its oxides, especially in water. Previous attempts to electrochemically reduce molybdenum from molybdate (Mool·) ions to molybdenum metal have reported the production of either a poorly adherent mixed oxide [4-6], or a thin(< 0.1 µm) metallic film [7-9]. Thick metallic molybdenum is capable of being co-deposited with one of the iron-group metals (Ni [10], Co [11] and Fe [12]) to produce an alloy [13, 14]. These alloys, however, may not be suitable for applications requiring pure molybdenum as they usually contain less than 50% molybdenum (often less than 30%)."

Jan 1, 2012

By Karin Soldenhoff

Recovery of uranium in conventional ion exchange circuits, using strong base or weak base resins containing quaternary or tertiary amine functional groups, is based on an anion exchange mechanism. In saline liquors, chloride competes with uranium for the active resin sites and reduces resin loading. This results in significant negative impacts on the IX process in terms of plant throughput and operating costs. In this paper we present the results of a study on the recovery of uranium from an acidic in situ leach liquor containing approximately 9 g/L chloride. A range of resins was tested, and a high capacity strong base resin was identified with significantly enhanced loading compared to conventional resins. Other process-relevant criteria such as loading kinetics and elution efficacy are also discussed. The process developed was successfully tested during a recent ion exchange pilot plant operated in conjunction with a field-leach trial.

By Gerald Onyedika, Tochi Onwumere, Martin Ogwuegbu

"The kinetic study for the leaching of iron from cassiterite ore in KOH solution was studied. The effects of KOH concentration, particle size and reaction temperature on the leaching rate of iron were also examined. The results of leaching studies showed that the leaching of iron from cassiterite ore in KOH solution is significantly influenced by the reaction temperature, KOH concentration, and decrease in particle size. The study showed that 90.62% of iron ore was leached in 8M KOH solution at 80°C within 120 minutes. The experimental data were well evaluated using the shrinking model for surface chemical reaction and diffusion control through the product layer. The activation energies for the iron ore dissolution using the two models were calculated to be 32.06KJmor1 and 97.97 KJmor' respectively.IntroductionIn recent times, there has been increasing attention on the kinetic study of mineral dissolution. In most of these studies, the experimental results were analyzed with a suitable shrinking core model under the assumption that the ore is a homogeneous spherical solid phase [1-4]. A study of the dissolution kinetics of a Nigerian cassiterite ore by hydrochloric acid showed that increase in the hydrochloric acid concentration is accompanied with increase in the amount of cassiterite ore dissolved at various times [4]. The optimal concentration was found to be 4.0M HCl, after which there was a decline in the amount of the ore dissolved, which showed that the concentration of the reagent has a significant effect on the leaching rate of the ore. Also in studying the effect of stirring speed on the rate of cassiterite ore dissolution while keeping other conditions constant for 120 minutes, the result showed that the rate of cassiterite ore dissolution was dependent on the stirring speed over a range of 0 to 630 rpm. Above 360 rpm, the stirring speed no longer had any effect on the solid dissolution. The dissolution rates of cassiterite were analyzed using a suitable shrinking model. The results showed that the reaction was controlled by the diffusion of tin through the porous product layer, a reaction order with respect to hydrogen ion concentration of 0.92 M and activation energy of 50.05KJmor'. In another kinetic study on the leaching of a low grade niobium-tantalum ore with concentrated KOH solution the effect ofreaction temperature, KOH concentration, agitation speed, particle size and alkali-to-ore mass ratio on the dissolution rate of niobium were examined [5]. The result of niobium leaching from low grade niobium-tantalum ore with concentrated KOH, solution at different agitation speeds showed that the dissolution rate increased with increase in agitation rate. In the case of particle size effect, the results show that small particles require much shorter time for complete dissolution than the large ones."

Jan 1, 2013

By Bora Derin, Sertac Yazici, M. Seref Sonmez

"In this study, the recycling conditions of waste liquor obtained after the production of tungsten boride powder from calcium tungstate by self-propagating high temperature synthesis (SHS) and the following hydrochloric acid leaching were investigated in detail. Environmentally unfriendly and extremely acidic (pH~ -0.3) liquor consisting of calcium, magnesium, and boron ions was treated with 1 M sodium carbonate solution to precipitate magnesium carbonate and calcium carbonate phases. The obtained amorphous precipitates were heated up to the temperature of 400°C for re-crystallization. As a result, MgO, CaC03 and CaMg(C03)z phases were obtained, while sodium, boron, chlorine ions were remain in the solution. The present study is still in progress.IntroductionSelf-propagating high temperature synthesis (SHS) is one of the techniques used in the production of a variety of advanced ceramics, inter-metallic, organic and inorganic compounds, oxygen free single crystals, and polymers [ 1, 2]. The reaction becomes selfsustaining and propagates in the reactant mixture, after initiation in SHS process. SHS products may contain the mixture of several unwanted compounds and elements. Therefore following acidic leaching process may be needed to purify the target product. In the previous study, calcium tungstate (Ca W04), magnesium (Mg) and boric acid (B20 3) mixture were reacted to produce tungsten boride powder by SHS process according to the Reaction 1. Then, magnesium and calcium containing byproducts (i.e. MgO, Mg3B206 and Ca3B206) found in the SHS product were leached out by using concentrated hydrochloric acid (HCl) solution to obtain pure tungsten boride powder [3].Ca W04 + 0.5B203 + 4.5Mg = WB + 4.5Mg0 + Cao (1)After the leaching, filtrate solution consisting of different amounts of magnesium, calcium, and boron requires additional treatment for the environmentally acceptable disposal.Several works were carried out about magnesium precipitation conditions and kinetics from brines. Rabadzhieva et al. investigated the precipitation of Mg(OH)z from brines by using NaOH as well as caustic soda [ 4]. Turek ve Gnot investigated the precipitation efficiency of Mg(OH)z for the temperature range between 10-40°C, while the reaction was kinetically experimented by Alamdiri et al [5, 6]. Homogeneous precipitation of nesquehonite (MgC03.3H20) by the reaction of MgCli with (NH4)2C03 in supersaturated solutions and factors that influence the precipitation of MgC03.3H20, such as reaction temperature, initial concentration, stirring speed, titration speed, equilibration time, have been studied by Wang et al [7]. The precipitation of Mg(OH)z by calcium hydroxide from aqueous solutions was studied by Baird et al. [8]. Stratful et al. focused on conditions influencing the precipitation of magnesium ammonium phosphate from wastewaters [9]. 1031"

Jan 1, 2011

By Matthew Tunnicliffe, Akram Alfantazi, Paul Nesbitt, Farzad Mohammadi

"Lead and its alloys are proper candidates for anodes in electrowinning processes mainly because they are insoluble in the leach solutions and relatively cheap. However, the annual cost of corrosion problems associated with these anodes is millions of dollars. In this study lead-silver and lead-calcium anodes were tested under typical nickel electrowinning conditions and the effect of chloride on the corrosion performance of the anode materials was investigated. Corrosion rates of the anodes were calculated using the discharge plateau (reduction of lead dioxide to lead sulfate) after galvanostatic experiments. It was found that lead calcium anodes have the highest corrosion rate both in the presence and absence of chloride. Surface morphology of the electrodes was studied using SEM and the corrosion products were characterized using XRD.IntroductionLead (Pb) is usually the preferred material for commercial anodes since it is insoluble in the leach solution and the costs are manageable. One advantage of using an insoluble material as an anode is the higher purity of the cathodic deposits and better quality of the end product. During nickel electrowinning, metallic nickel is deposited on the cathode while oxygen evolution reaction (OER) takes place on the anode. In practice, relatively high potentials are necessary for the reaction to proceed at the desired rate because of the high overpotential of OER on lead. Lead anodes get oxidized in typical electrowinning conditions and usually have two to three years of lifetime. Although the price of each anode is insignificant, the overall cost of corrosion of these anodes is considerable, which is due to the large number of anodes used in a plant, typically two to three thousand. Therefore, corrosion is a significant problem associated with lead anodes in commercial nickel electrowinning plants and industries show interest in addressing this problem. Corrosion of lead electrodes in acidic environments has been previously the subject of many research studies [I-7]. It has been reported that, during the anodic polarization of lead, several phases may be present on the surface, depending on the potential range that is being studied [8]. Lander showed that lead is oxidized at potentials higher than 0.252 YsHE with tetragonal lead monoxide being the main reaction product [9]. At 0.666 YsHE lead can transform to lead dioxide; however, it is not stable and transforms to lead sulfate and lead oxide. At potentials higher than 1.684 YsHE, lead dioxide is eventually a stable phase and forms a protective layer on the surface [I 0, 11]. Under conditions of a typical nickel electrowinning plant, usually a 200 A/m2 current density is passed through the electrodes."

Jan 1, 2012

By M. I. Novgorodova

Most of the gold in the earth&apos;s crust occurs as finely-dispersed gold and accounts for much of the gold lost in extraction processes and during exploration for gold. The Compositions, sizes, and morphology of fine gold particles (0.01 to 10 ~m in diameter) were studied with high resolution electron microscopy coupled with electron microprobe and microdiffraction devices, using colloidal carbon replicas. Correlations were made between fine gold, mineral associations and ore genesis. The results provide qualitative information on the proportions of finely dispersed, invisible and visible gold distribution in ores. Such knowledge is fundamental when planning an optimum technological recovery process.

Jan 1, 1991

By M. Arenas

A corrosion study of a bonded NdFeB permanent magnet materials alloyed with titanium carbide additions has been undertaken. The materials were produced by rapid solidification by melt spinning. Commercial epoxy was used as a bonding medium. The corrosion results were compared with those of a near stoichometric unalloyed NdFeB. Anodic polarization and potentiostatic techniques in 0.9 M Na2SO4 solutions were used to characterize corrosion behavior. It was found that the addition of 6 a10 Tic resulted in superior corrosion resistance, as indicated by lower corrosion currents and less iron dissolution at fixed potential.

Jan 1, 1997

By Gunther Klamp

Disposal of arsenic compounds from washing acid in metallurgical plants is becoming a severe problem when using lime neutralization. A further problem is the disposal of relatively large quantities of gypsum which is produced during this neutralization step and which Is also conta-minated with other toxic metal compounds. The Sachtleben-Lurgi process removes arsenic and other metals from washing acid in the form of insoluble sulphides. The purified acid contains less than 0.5 ppm of arsenic and can be used for standard sulphuric acid applications. The process Is demonstrated commercially at Sachtleben&apos;s acid plant since more than five years.

Jan 1, 1992

By A. I. Okunev

The investigation results are submitted on separation into layers in the systems Cu (Ni) - Fe - Ca - 0 - S - (Si), as well as on physico-chemical properties of oxide - ferrite, oxide-sulfide melts (density, surface tention, viscosity, electric conductivity), on kinetics and oxidation macromechanism of iron and sulfur in the oxide-silicate, oxide-ferrite and oxide-sulfide melts, kinetics of reduction of oxide-silicate and oxide-ferrite systems. Conditions are discussed for copper, nickel and zinc recovery from oxide-silicate and oxide-ferrite slag in liquid and solid states. Some promising technique is the technique of future, as is considered.

Jan 1, 1988

By R. J. Dippenaar, W. H. Van Niekerk

"An injectable lime-based desulphurization reagent for the treatment of liquid iron was developed. Firstly, selected lime based slags containing small quantities of CaF2 to increase fluidity, and Na20 to increase the basicity, have been evaluated on laboratory scale from a thermodynamic point of view. Subsequently, pilot plant and full scale industrial injection trials were conducted. It was found that lime-based slags, containing Na20 and CaF2, are able to desulphurize liquid iron efficiently. By the injection of a lime based reagent consisting of 60% lime, 25% soda ash and 15% fluorspar at a rate of 7 kg reagent/ton hot metal, the sulphur level in the metal (115kg) was reduced from 0,07% to 0,01 % within 5 minutes. The lime-based reagent developed in this study was successfully injected, both from a metallurgical and from a pneumatic point of view, on an industrial scale. The mathematical model utilised in this study, can be used successfully to predict the course and extent of desulphurization by lime-based slags. IntroductionMainly due to environmental difficulties encountered with pure soda ash, dry slag formation with CaC2 and high cost when Mg are used as desulphurizers, much incentive exists for the development of an inexpensive, environmentally friendlier desulphurization reagent. As a first step in the development of such a reagent, selected lime based slags containing small quantities of CaF2 to increase fluidity, and Na2O to increase the basicity, have been evaluated on laboratory scale from a thermodynamic point of view. This was followed by pilot plant injection experiments in which the kinetics of the relevant desulphurization reactions were evaluated. Finally, full scale industrial trials were conducted. All three phases of the investigation will be discussed with the major emphasis being placed on the kinetic study."

Jan 1, 1996

By Kimio Ilagaki

The distribution ratios of Ag, Pb, As, Sb and Bi for the Cu2S-FeS or Ni3S2-FeS matte I FeOx-SiOl, FeOx-Si02-CaO or FeOx-CaO slag equilibration in a MgO crucible were determined experimentally at 1523 ~1573K under controlled partial pressures of S2 and 02 at given PS02 of 10.1,50.7 and 101.3 kPa(O.I, 0.5 and I atm), and the observed dependency of distribution ratio on the matte grade, S02 pressure and slag basicity were analyzed on the basis of thermodynamics.

Jan 1, 2003

By Laihua Wang, Peter Hayes, Hae-Geon Lee

"This paper introduces a new process for the efficient removal of dissolved gases and inclusions from liquid metals. This process involves the creation and dispersion of fine bubbles in molten metals by introducing inert or reactive gas into a region of turbulent flow. The highly turbulent metal flow splits the gas into fine bubbles and results in good mixing between the gas and molten metal phases. These conditions are ideal for contacting inclusions in the metal with the bubbles and subsequent flotation of the inclusions to the metal-slag interface where the inclusions are then absorbed by the covering slag layer. Dissolved gases, such as [H], [0], [N] in the metals are also transferred to the gas bubbles and removed from solution.The process concept has been previously demonstrated using a full-scale air/water model to simulate the ladle-to-tundish system of continuous casting of steel. The present cold modelling work has further demonstrated the ability of the process to remove gas solutes. The results indicate that the efficiency of new process is several hundred times greater than that of conventional high speed rotating injectors which are currently applied in the treatment of liquid light metals.IntroductionDuring metal smelting, refining and alloying processes, unwanted gas and second phase liquid or solid impurities are incorporated into liquid metals. In the case of steelmaking, the gas-forming impurities include [0], [H] and [N], and the solid impurities as a result of deoxidation include Ah03, Si02 inclusions. Common impurities in liquid aluminium are dissolved hydrogen and solid Ah03. To avoid subsequent problems during processing and to improve the physical properties of the metal products it is necessary to significantly reduce the level of impurities."

Jan 1, 1996

By Dean G. Heitt

"The Rain and SMZ mines from 1987 to 1994 produced a total of22.0 t of gold from a pre-mine reserve of 14.24 Mt of ore grading 2.13 g/t Au.Gold at Rain is hosted within the basal portion of the Mississippian Webb Formation. ·Mineralization is closely tied to the Rain Fault which is interpreted to be the main feeder for the deposit. Multiple collapse and hydrothermal breccia events provided permeability for the mineralizing fluids in the otherwise unreactive siltstones. Major alteration events include: decalcification and dolomitization of the Devils Gate Limestone; and silicification, baritization, argillization and oxidation of the Webb Fm. Six ore types based on XRD and visual rock chip Jogging have been identified: siliceous ore containing >40% quartz and <30% barite; siliceous-baritic ore containing mostly silica but >30% barite; baritic ore containing >40% barite; argillaceous ore containing >40% total clays (including alunite); calcareous ore containing mostly calcite and dolomite; and carbonaceous ore which has significant pyrite and organic carbon. Metallurgical testing of the oxide leach grade ores found that recoveries, on -1.3 cm crushed material, were greater than 70%. Results also found that Rain ore has strong grind dependency due to silica encapsulation.The Rain leach pad was commissioned in 1988, and to date 9.3·Mt at an average grade of0.65 g/t Au have been placed. Life to date recovery, through December 1995, is approximately 51 %, for a total of3.87 t of gold produced. Two major factors have contributed to the low leach recoveries at Rain when compared with the metallurgical testing: 1) More argillaceous ore than expected was placed on the pad especially late in the mine life and 2) approximately 50% of the tons placed were run-of-mine with no agglomeration."

Jan 1, 1997

By D. J. Adams

Cyanide heap leaching is the predominant technology used in processing low-grade gold ores. During closure ora heap leach operation, residual cyanide must be removed from the process and waste solutions, as well as the heap. Biological cyanide oxidation is a proven, economical technology for destroying cyanide in process and waste waters and spent heaps; The use of biological cyanide degradation eliminates the need for toxic or corrosive chemical oxidizers and has- been implemented at full scale at treatment costs usually <$0.50/1,000 gal. The Applied Biosciences biological cyanide destruction (BCND?) process has been demonstrated to effectively treat cyanide, concentrations up to 350 mg/L. Treated process solutions and wastewaters also contained other contaminants such as arsenic, copper, iron, silver. selenium, mercury, nitrate and zinc, much of which was removed in the cyanide degradation process. Under optimal conditions, microorganisms can rapidly oxidize free cyanide in some process solutions from over 250 mg/L down to 0.1 mg/L in 4 to 5 hr. Cyanide is degraded to ammonia and carbon dioxide, with 50%ofthe cyanide carbon liberated as C02. In general, carbon tank based bioreactors degrade cyanide at significantly higher rates than process or wastewater pond configured treatments, which usually degrade cyanide-more rapidly than in heap treatments. Investigation of cell-free enzyme preparations as an alternative to live microbial cyanide degradation shows promise. Advantages of enzymes over live microbes for cyanide degradation include: (I) the ability to tolerate and degrade higher cyanide concentrations (> I ;000 mg/L), (2) nutrients to support live microbial cells are not required, (3) the effects of other toxic contaminants, such as metals, found in mining waters-are eliminated and (4) the potential for greatly increased kinetics.

Jan 1, 1998

By J. V. Happ

The investigation reported in this paper was prompted by the belief that vacuum processing of copper mattes could provide significant advancement to present-day copper smelting and converting technology. Specifically, vacuum distillation of copper mattes in a unit such as the R.H. vessel used in vacuum degassing of steel, can lead to improvements in: converter flue-gas-cleaning system, purity of acid (or liquid SO2), aisle hygiene, purity of electrorefined copper and smelter flexibility. In the study conducted, removal of Volatile impurities (arsenic, antimony, bismuth, lead and zinc) from liquid mattes, by vacuum distillation in a laboratory-scale equipment was performed. The conditions investigated covered a temperature range of 1123-1223K, absolute pressure of 6.5-0.5kPa (50 - 3 mm Hg) and with bleed gas consisting either of pure oxygen or argon. Six matte samples (four U.S. and two foreign) were tested. Under the "best" conditions arsenic and antimony were reduced to << 0.01% in the product matte. The removal of bismuth, lead and zinc was variable and appeared to be influenced by the matte composition of the sample. As might be expected, the rates of distillation of the various species were increased at higher temperatures and lower absolute pressures. The influence of a small flow rate of gas (02 or Ar) over the melt did not have a signifi¬cant influence on the extent of impurity removal. The magnetite content of the matte was reduced by up to 30% during vacuum treatment and was favored by a low partial pressure of oxygen over the melt. Substantial amounts of sulfur were also evaporated and an, overall increase in copper grade of the matte was realized. The paper concludes with an evaluation of industrial aspects of the process as applied to conventional smelters.

Jan 1, 1983

By G. P. Chaudhari, F. Warchomicka, M. Dikovits, V. Pancholi, C. Poletti

"The hot formability of a microalloyed steel with 0.16 wt-%C modified with N is studied by using processing maps. Compression tests of cylindrical samples are carried out using a Gleeble®3800 simulator in the range of temperature between 750 -1000°C and strain rates between 0.01-100 S-1. For this alloy, an Ar3-temperature about 740°C is determined by means of dilatometry. Processing maps are calculated using the modified dynamic material model developed by Murty and Rao for different logarithmic strains. For the instability map, the parameter Kj developed by the authors in previous works is used and compared with other instability values. Softening in the flow curves provoked by induced ferrite during deformation at low temperatures and low strain rates is reflected in the n-value. Light optical microscopy (LOM) and electron back scattered diffraction (EBSD) measurements are used to study the microstructure of the hot deformed samples to determine the deformation mechanisms active and to verify the processing maps.IntroductionProcessing maps offer a good possibility to optimize thermomechanical process parameters and to avoid defects in the products. Prasad et al. [1] developed the processing maps using the dynamic material model (DMM) and Murty & Rao [2] modified it. Processing maps consist of two superimposed maps: the dissipation efficiency and the instability map. The processing maps can be used to detect areas with a good hot formability, which are normally related to restoration of the material by dynamic recovery/recrystallization. For a high dissipation efficiency value and no instabilities, a good hot formability is predicted. In the DMM no storage of energy takes place and so the material is considered essentially dissipative, this is only true for high temperatures and high strain rates [1]."

Jan 1, 2012

By Taner Kavas

The refractory bricks of a rotary cement furnace containing of alumina and magnesium chromite were studied in order to determine whether they could be used in the concrete production as aggregates. Three mortars were prepared by mixing 1 part cement, 3 part aggregate materials, 0.5 part water by weight and mechanical, chemical, thermomechanical and microstructural characteristics were evaluated. The compressive and bending strength of samples were determined after 2 and 28 days curing. Resistance to chemicals were established by calculating the weight gain of mortars stored in 2 % HCl solution for 1 h and 24 h. Thermomechanical characteristics were determined by measuring the compressive strength of heat treated specimens at temperatures of 400 °C, 600 °C and 800 °C. Consequently, magnesium chromite containing waste brick aggregates have given the best results.

Jan 1, 2006

By K. Watling

Vibrational spectra of surface and solution compounds formed during cyclic voltammetry of a gold electrode in a deoxygenated 0.01 mol dm-3 NaCN solution have been examined using surface-enhanced Raman scattering (SERS) spectroscopy. The presence of cyanide at the electrode surface was indicated by Raman bands characteristic of the carbon-nitrogen stretch, CN.. Chemisorption of cyanide on the gold surface was evidenced by the presence of vibrational modes due to gold-carbon stretching, AuC, and gold-carbon-nitrogen bending, AuCN. Prior to the disappearance of the surface cyanide stretch band, a limiting value of the CN was obtained, the same as the value reported for adsorbed cyanide. Effects upon the voltammetry and vibrational modes of surface species due to additions of silver and lead to the gold-cyanide system have been observed.

Jan 1, 2003

By Mariana Barcelos, Frederico Muylaert Margem, Giulio Rodrigues Altoé, Pedro Amoy Netto, André Gomes, Sergio Neves Monteiro

Environmentally correct composites, made from natural fibers, are among the most investigated and applied today. In this paper, we investigate the mechanical behavior of polyester matrix composites reinforced with continuous fique fibers, through bending tensile tests. Specimens containing 0, 10, 20 and 30% in volume of fique fiber were aligned along the entire length of a mold to create plates of these composites, those plates were cut following the ASTM standard to obtained bending tests specimens. The test was conducted in a Instron Machine and the fractured specimens were analyzed by SEM, the results showed the increase in the materials tensile properties with the increase of fiber amount.

Jan 1, 2015