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By L. A. André Santos

Atmospheric processing of nickel lateritic ores with low costs has been encouraged. In this work the kinetic of atmospheric acid leaching of a northern- Brazilian ore with 1.63% Ni and large amount of fine particles (d50 ≈ 0.075 mm and 40% below 0.038 mm) is presented. Chemical analysis showed a trend of Ni and Fe concentration in finer fraction (−0.075 mm) and Si and Mg in the coarsest one (−0.500 + 0.150 mm) associated to distinct mineral phases. Nickel is widespread in the mineral matrix. Distinct behaviors were observed as a function of particle size associated to the distribution of silicates and iron oxides in the ore. The kinetic modeling indicated that leaching is controlled by porous layer diffusion at 65 °C, but at 95 °C exhibits a mixed control by porous layer diffusion in initial minutes (60 min) and by chemical reaction or diffusion through the pore layer in final minutes (60–240 min) depends on metal evaluated.

By Junmo Ahn

This study investigated leaching kinetics by alternative lixiviants for copper leaching from chalcopyrite (CuFeS2), the most abundant copper resource in the world. As a refractory sulfide mineral, chalcopyrite shows low copper extraction due to passivation on chalcopyrite surface. Also, decrease of copper grade with high portion chalcopyrite requires the alternative leaching procedure to increase copper recovery. Therefore, alternative lixiviants such as sulfurous acid and methanesulfonic acid (MSA) were tested for both concentrate and low grade ore to enhance copper extraction. Also, an oxidant, hydrogen peroxide, was compared to ferric to find out the improvement of leaching kinetic. In concentrate leaching tests, 30 g/L MSA showed the highest copper extraction (47%), compared to other lixiviants at 75 °C. Periodical H2O2 addition enhanced copper extraction, and above 90% of copper extraction was observed within 96 h by periodical addition of 0.6% H2O2 at 75 °C. The activation energy of chalcopyrite leaching by MSA and H2O2 achieved 40 kJ/mol, which is chemical reaction control. The results of low grade ore leaching tests indicates that no significant difference among lixiviants (H2SO4, H2SO3 and MSA) with ferric was observed, all of which achieved around 37% within 24 h at room temperature. However, significant increase of copper extraction (>80%) was observed at both 20 g/L MSA and 10 g/L H2SO4 conditions by the addition of 10% H2O2.

By Rajashekhar Marthi

Lithium is a key component for future electric vehicle batteries and energy storage. The future availability of lithium to meet the growing demands remains in question. Around 60% of lithium resources exist in the form of continental brines. Traditional methods to recover lithium from brines use solar concentration with precipitation and have found limitations in lithium extraction due to interference of Mg in high Mg/Li brines. Thus, there is a need for highly selective adsorbents. Recently, spinel structured delithiated lithium manganese oxides have demonstrated promising results. However, due to the small particle sizes, it is economically difficult to recover the adsorbents and thereby limits industrial applications. In our work, LiMn2O4 ion sieve was synthesized and immobilized on diatomaceous earth. Fundamental adsorption studies were carried out in lithium buffer solutions to understand the nature of adsorption and kinetics. The adsorbents were also tested for recycle stability, as well as recovery of lithium from Great Salt Lake water samples.

By Norman Schapiro

Future ore bodies will, most likely, be more costly to find, mine and process than those now in production because most of them will be of lower grade or found deeper. To evaluate an ore deposit for extraction of metal values it is important to select the optimum economic process from among the many available options. The physical and chemical behavior of the minerals present should govern the process selection. Process mineralogy which combines mineralogy and petrography with process development engineering generates the data on mineralogy, composition and texture of gangue and valuable minerals from which the optimum process steps can be selected in the commercial design of the ore processing plant. These insights also help in solving operating problems caused by changes in the ore body

Jan 1, 1981

By C. Dupuis

Thiourea is a promising reagent for gold extraction especially from refractory ores that cannot be treated by traditional cyanidation route. In this study recovery of gold from thiourea leaching solutions was investigated by direct electrowinning. The electrolysis cell consisted of a carbon flow-through cathode and a lead anode. The anodic and cathodic compartments were separated by a membrane. Galvanostatic mode was chosen for operation of the cell. Factors affecting recovery efficiency such as cathode thickness, linear flowrate, current intensity, thiourea and gold concentrations were investigated. The influence of some species in solution on efficiency and selectivity of recovery was investigated. Gold recovery reached 99% but current efficiency was lower than 10%. The complex formed with ferric ion and formamidine disulfide are reduced before gold-thiourea complex. Thiourea consumption occurred during leaching mainly by oxidation and reaction with dissolved copper.

Jan 1, 1989

By M. R. Baren

Unpublished results obtained by Baren on thermodynamic properties of sulfur in liquid Fe. Co. Ni. Fe-Co. Fe-Ni. and Co-Ni are reevaluated. correlated. and interpreted on the basis of recent developments in thermodynamics of alloys:. Existing reliable data are reviewed and compared with the? present results. Sulfur obeys Henry's law up to 0.04 mol fraction. and in this range the standard Gibbs energy of solution of sulfur is expressed as a linear function of temperature for each pure metal. The activity coefficient of sulfur in each binary metal solvent 1s correlated with the composition of alloy.

Jan 1, 1983

By Lijun Lu, Honghui Fang

This article carried out the experimental study on using desulfurization ash in steel slag composite material. This was done by investigating the desulfurization ash content in formula one and formula two samples on the influence of setting time and strength of mortar. Through this study the following conclusions were reached for formula one: (1) a setting time of more than 10 hours is required, (2) a dosage of desulfurization ash of 1 ~ 2% is optimal, where flexural strength is reduced by 10% ~ 23% and compressive strength reduced by 5.7% ~ 16.4%. The conclusions of formula two were: (1) when the dosage of desulfurization ash is within 5%, the setting time is within 10 hours; (2) when the dosage of desulfurization ash is 1 ~ 2%, the flexural strength is increased by 5 ~ 7% and the compressive strength is reduced by 1 ~ 2%. The results show that the formula two is better.

Jan 1, 2015

By Satu Strömberg

A single-particle laminar-flow technique was used to study oxidation of two nickel concentrates and a granulated nickel matte (43 wt% of Ni). Experimental conditions were: reaction gas from N2 to N2 + 75 vol% O2; gas preheating temperatures ranging from 500 to 1100°C. The major nickel-bearing minerals in the two concentrates were pentlandite and violarite, respectively. Chemical analysis of the particles was used to determine the oxidation degree of the materials, and optical and scanning electron microscopy were used to detect their morphology and mineralogy. Total desulfurization of the nickel concentrates was achieved under the most oxidizing conditions, while the sulfur removal from the nickel matte was not as efficient, especially with the coarse size fraction. Pentlandite-based concentrate was found to be less reactive than the violarite-based.

Jan 1, 1995

By Yoshinobu Fukumori, Testuya Watanabe, Futoshi Shikata, Hiroyuki Tokumitsu, Hideki Ichikawa, Masahito Miyamoto

Nano-particulate systems have attracted much attention recently in pharmaceutical field as drug carriers and functional components of pharmaceutical dosage forms. This paper describes our approaches in design and preparation of nano-particulate systems, including lipid nano-emulsions, chitosan nanoparticles and thermosensitive acrylic nanoparticles, for certain pharmaceutical applications mentioned below. The lipid nano-emulsions with their particle size smaller than 100 nm were prepared for gadolinium neutron-capture therapy (Gd-NCT) of cancer by a thin-film hydration method with sonication, and intraperitoneally injected into Greene's melanoma (melanotic No. 179)-bearing Syrian hamsters. This provided such a high gadolinium concentraton in tumor as 107 µg/g tumor (wet basis) at 48 h after administration. As an alternative gadolinium nano-carrier for Gd-NCT, biodegradable and highly gadopentetate-loaded chitosan nanoparticles (Gd-nanoCPs, 426 mTI in particle diameter and 9.3% in Gd content) were prepared by a novel emulsion-droplet coalescence technique. A significant tumor-killing effect could be obtained when Gd-nanoCP suspension was injected intratumorally twice 24 and 8 hours before neutron irradiation into B 16Fl O melanoma-bearing mice and subsequently thermalneutron was irradiated toward tumor site with a flux of 2 x 109 n/cm2/sec for 60 min. As one another application of nanoparticles, a novel acrylic composite latex with a hydrophobic core and a thermosenstively swellable shell was designed for fabricating microcapsules showing thermosensitive mode of drug release. The microcapsules with the composite latex-dispersing membranes exhibited an exceptionally rapid on-off response of drug-release in a thermosensitive manner.

Jan 1, 2000

By Jr. Langhans, J. S. McPartland

"The presence of zinc in cyanide solutions is generally thought to not have an adverse effect on precious metal recovery or recovery rate by heap leach processing. However, analytical interferences of zinc in solution can cause problems in accurately determining and controlling cyanide concentration in the leach solution, leading to increased cyanide consumption. Analytical methods and the chemistry of cyanide in the presence of zinc are reviewed. The effects of solution pH and zinc concentration on the free cyanide determination were evaluated in detail. Use of the standard silver nitrate titration and a modified titration method for controlling cyanide concentration during heap leaching were investigated experimentally. The practical implications of cyanide heap leaching in the presence of cyanide soluble zinc minerals are discussed.IntroductionThe presence of zinc in precious metal cyanidation circuits is not uncommon. Zinc can be introduced into cyanide leach solutions through dissolution of various zinc minerals1>, or through the use of a Merrill Crowe (zinc precipitation) circuit. Zinc minerals typically occur infrequently and in low concentration in gold ores, but are more abundant in silver ores. Merrill Crowe systems are most commonly employed for recovery of precious metals from solution for relatively high silver ores. It is desirable to control the amount of dissolved zinc in a cyanidation circuit for several reasons. Excessive zinc build-up in cyanide leach solution can, under certain circumstances, inhibit precious metal dissolution and adversely affect solution recovery systems. Additionally, high zinc concentrations can lead to excessive in-process cyanide inventories and potentially, to higher cyanide consumption"

Jan 1, 1999

By Jing Zhan, Chuanfu Zhang, Yonglin Yao

"The Ni/Co arbitrary ratios of fibrous precursor were investigated during coordinated coprecipitation by changing the precipitating medium. The results show that the original molar ratio ofNi2+ to Co2+ in reaction solution can be maintained in the coprecipitate at pH'.'05.0 and the coprecipitate is single phase solid solution using water and water-X precipitating medium. But the original Ni/Co ratios are no longer kept and composition of the coprecipitate is not uniform at pH>5.0 in water precipitation medium. In order to obtain the precursors with the required morphology and accuracy Ni/Co ratios, the optimum conditions of fibrous precursors were chosen as follows: ammonia used as complex agent and pH adjustor, water-X solvent as precipiting medium, oxalate as coprecipitated agent, 8.0-8.4 for pH value, 50-70°C of reaction temperature, 0.5-0.8 mol/L of initial nickel and cobalt salt concentrations and excesses of oxalic acid of 10% - 20%.IntroductionNi-Co alloy as an important transition metal alloy with high mechanical strength, good anti-deformation, corrosion resistance, thermal conductivity, thermal stability, electrical conductivity, electrical contact, and special magnetic properties indicates that it can be used as high-temperature catalyst, special magnetic material, high-temperature electrochemical devices, and so on [1-6]. An ideal composite powder should have an appropriate stoichiometric ratio, good uniformity of chemical composition, appropriate phase, low impurity content and small particle size [7]. Similarly, the composition of nickel-cobalt alloy powder has an important impact on its crystal structure, properties and applications. Guo[8] found that magnetisms of CoxNi1-x such as magnetic anisotropy, curie temperature, and the shifts of the spin steering are very sensitive to the composition of alloy powder."

Jan 1, 2013

By Stanko Nikolic

The Top Submerged Lance (TSL) technology, developed in the 1970s, is now widely used for the processing of a range of materials. TSL technology for continuous converting was first patented in the 1990s. The process is based on the use of calcium ferrite slag. Although this slag system had been applied elsewhere the phase equilibria had not been thoroughly investigated. This lead to a collaboration between the Process Technology group of Mount Isa Mines, now part of Glencore, and the Pyrometallurgy Innovation Centre (PYROSEARCH) at The University of Queensland. Through multiple research programs this complex system was successfully investigated. The results were then implemented within thermodynamic modelling tools. This combined new knowledge was then applied to the design and industrial implementation of the TSL continuous converting technology, ISACONVERT™. This paper describes the key findings of the research and how this was applied to the industrial implementation of the technology.

By W. E. Wallace, J. A. Warren, D. Josell, D. Wheeler

"We present the results of experiments and modeling of flip-chip geometry solder joint shapes under shear loading. Modeling, using Surface Evolver, included development of techniques that use an applied vector force (normal and shear loading) as input to determine a vector displacement of the pads connected by the solder joint (standoff height and misalignment). Previous solutions solved the converse problem: fixed displacements used to determine required applied force. Such solutions were inconvenient for applications, where the applied force (chip weight) is known. Also, for geometric and materials studies of solder joint shapes involving multiple parameters, determining the equilibrium displacement from applied force by bracketing solutions could become computationally expensive. Measurements of solder joint standoff height and misalignment as functions of the applied force (normal and shear), solder volume and pad diameter are presented. Experiments were carried out for solder ball diameters from 0.38 mm (0.029 mm3 volume) to 0.15 mm (0.0019 mm3 volume) on pads of diameter 0.64 mm and 0.35 mm. Fitting of simulation to experimental results gave optimized values for the contact angle and surface tension of the solder which were consistent with measured and literature values. IntroductionIn packaging technology flip-chip has become an important method for attaching semiconductor devices to substrates. Generally, the chip and substrate are bumped with solder and then the chip is flipped onto the substrate and the solder reflowed to form conductive interconnects. An epoxy underfill is normally flowed between the substrate and chip to reduce the thermal fatigue on the solder joints. A flip-chip assembly is illustrated in Figure 1.In flip-chip applications, the use of an integrated underfill/solder bump system [1, 2) removes an extra process step, namely infiltration of the underfill. However, the presence of an underfill will retard the self-alignment of the flip-chip. A first step in understanding and predicting this retardation is to develop a model to describe normal and lateral force-displacements curves when underfill material is not present. At this stage it is unclear whether static surface tension theory is sufficient to describe a complete model for flip-chip realignment even without underfill."

Jan 1, 2001

By Lucas Barbosa de Souza Martins, Felipe Perissé Duarte Lopes, Nathalia Carneiro Garcia Rosa, Lucas Lopes da Costa, Sergio Neves Monteiro, Rubén Jesus Sanchez Rodriguez

"The fibers extracted from the stem of the banana plant are relatively stronger and have been used as reinforcement of polymer matrix composites. In addition to quasi-static mechanical properties, there is a need to characterize the dynamic behavior of banana fiber composites subjected to thermal and mechanical constraints. In this work, the temperature variation of the dynamicmechanical parameters of polyester composites incorporated with up 30% in volume of banana fibers were investigated by DMA tests. The storage and loss moduli as well as the tangent delta were measured from 20 to 200°C in a TA Instrument operated with the flexural mode at 1 Hz. The results showed that the incorporation of banana fibers tends to increase the viscoelastic stiffness of the polyester matrix. It was also observed changes in the T g and the structure dumping capacity of the composites with increasing fraction of banana fibers.IntroductionNatural fibers with high amount of cellulose, also known as lignocellulosic fibers, have been used from primeval times by our civilization. In the last century, synthetic fibers such as nylon, carbon, aramid and glass fibers gained interest owing to superior strength and precise dimensional control. Natural fibers were then replaced by synthetics in many fields such as textiles and appliances. In the past decades, however, environmental issues drawn, once again, the attention to lignocellulosic fibers as possible substitute for intensive energy-consuming and long term polluting synthetics, specially the glass fiber [1]. In particular, research works have disclosed the potential advantages associated with the use of lignocellulosic fibers as the reinforcing phase in polymer composites [2-7]. Among the advantages it is worth mentioning the renewability, recyclability, biodegradability and the fact that natural fibers are neutral with respect to C02 emissions responsible for global warming. Moreover, as compared to synthetics, lignocellulosic fibers present lower density and cost as well as reduced wear caused to the processing equipment. On the other hand, in terms of composite reinforcement, hydrophilic lignocellulosic fibers present drawbacks such as weak adhesion to hydrophobic polymeric matrices in addition to dimensional limitations and non-uniform properties."

Jan 1, 2011

By Christiana Mystrioti

Greece is the only EU country with extensive nickel laterite deposits. Since the 1960s, the Greek laterites are treated for ferronickel production via a pyrometallurgical route, which involves pre-reduction of the ore in rotary kilns and reduction smelting in electric arc furnaces. Due to the rising cost of energy and the decreasing grade of mined laterites, the pyrometallurgical treatment is economically marginal. For this reason, alternative treatment processes are currently under investigation. Potential applicability of hydrometallurgical treatment, using either H2SO4 or HCl, under atmospheric pressure conditions, for Ni and Co extraction from two low grade laterite ores, was examined in the present work. The two samples were selected to represent the different mineralogical composition of the saprolitic and limonitic ore deposits of the Greek laterites. The investigated parameters were temperature (65–90 °C), acid concentration (1–4 N) and solid to liquid ratio (10–30% w/v). The results indicated that HCl was more efficient than H2SO4 for the treatment of the saprolitic ore; Ni and Co extractions were very high for both elements, up to 98% and 96% respectively, while H2SO4 could leach efficiently Ni, up to 100%, but extracted only 34% of Co. Hydrochloric acid was also more efficient for the treatment of the limonitic ore, with Ni and Co extractions up to 98.3% and 87.6% respectively. With H2SO4 the maximum extractions were 71.3% for Ni and 52.1% for Co.

By W. E. Straszheim

Computerized microscopic techniques were used to determine the size and identity of the ash-forming mineral components, as well as their association with the organic coal matrix, in order to aid in the development of physical methods of beneficiation which require such characterization for the most effective cleaning. Examples of particle size measurements, mineral phase identification, and especially coal-mineral association results are given for selected samples of raw and physically cleaned coals. These measurements can reveal certain characteristics of coals which can be be of significant value in predicting coal recovery and mineral matter rejection for coals undergoing beneficiation.

Jan 1, 1989

By David T. Hobbs

Large quantities of highly alkaline, radioactive, liquid wastes are stored in underground tanks throughout the Department of Energy complex. These wastes will be pretreated to separate radionuclides and the remaining decontaminated liquid wastes incorporated into solid waste forms for permanent disposal. Significant savings in disposal costs could result by recovering .the sodium as sodium hydroxide for reuse or disposal as nonradioactive waste. Recent testing demonstrated an electrochemical separation process for the recovery of sodium hydroxide from alkaline waste solutions; The separation process uses ion-selective membranes to separate sodium from the bulk of the waste constituents under an applied electrical field. The sodium is recovered as a 10-15 wt % solution of sodium hydroxide. Results of bench-sc3Ie and pilot-scale tests with simulated and radioactive waste solutions are presented.

Jan 1, 1999

By T. T. Lin, N. H. Madsen, K. Groom, B. A. Chin

"The objective of this research is to investigate the feasibility of using infrared sensors to monitor the welding process. Data were gathered using an infrared camera which was trained on the molten metal pool during the welding operation. Several types of process perturbations which result in weld defects were then intentionally induced and the resulting thermal images monitored. Gas tungsten arc using AC and DC currents and gas metal arc welding processes were investigated using steel, aluminum and stainless steel plate materials. The thermal images obtained in the three materials and different welding processes revealed nearly identical patterns for the same induced process perturbation. Based upon these results, infrared thermography is a method which may be very applicable to automation of the welding process.IntroductionAutomatic welding is commonplace in industry today. However, most, if not all, involves preprogramming for performance of a repetitive task. These systems are incapable of correcting for perturbations which arise during the welding process. Control of the welding process requires the identification and monitoring of perturbations in a wide variety of parameters. The varied nature of these parameters and the large number of variables involved have thwarted previous attempts at closed loop control of the welding process. The sensor(s) employed by a control system need to meet rather strenuous requirements. First and foremost of these is that such a sensor must be able to identify and discriminate between perturbations that might affect the quality of the weld, including such geometrical perturbations as a change of direction in the seam between the parts being welded, gaps in the seam or a misalignment of the parts being welded. The sensor should also be able to locate and identify contaminants and impurities in the weld puddle and ahead of it while monitoring the extent of the heat-affected zone and the cooling rate of the metal. The sensor(s) should, additionally, be able to perform these tasks in a time frame that is consistent with automatic control of the welding process. This paper presents results that could aid in the assembly of such a controlled welding system."

Jan 1, 1986

By Donghai Li, Cheng Pan, Pan Chen, Xuewei Lv, Mei Liu

"Chromite concentrate after beneficiation can not be directly used in the electric furnace. Therefore sintering is one of the effective way to agglomeration, by which the chromite concentrate can be utilized and the power cost of ferrochrome smelting can be reduced. The properties of raw materials and the sintering process of chromite concentrate were studied in this work. The results showed that chromite concentrate used can hardly granulated alone, while chlorite addition can improve the effect of granulation. Moisture plays an important role in sintering process. The granulation effect is optimal when the amount of water addition is 12%. Strength and abrasion index are the evaluation indexes of sinter quality. It was found that the strength of sinter increased with coke dosage increasing to 12%, and then decreased when it continuously increased. Opposite regularities were found for the abrasion index of the sinter.1 IntroductionChromium is a very important metal element which is mostly used in the production of stainless steel. In the earth, it is always formed compound with iron as ferrochromium spinel (FeO.Cr203), and its mineralogical name is chromite.[1] Currently, the global production of chrome ore is about 20 million tonnage every year , in which fine ore (less than 8 mm) accounted for about 80% [2] Although the price of the fine ore is cheaper than the lump one, too much fines will lead to the poor permeability and causes increased electricity consumption while producing ferrochrome. Therefore, the agglomeration process of chrome ore is one of the effective measures to increase the usage ratio of fine ore."

Jan 1, 2013

By Alexander Burns

Electrolytic salt splitting is a technology where acid and/or base is regenerated from a neutral salt using membrane electrolysis. Recent advances in the understanding of brine treatment, membrane stability, and cell design have made electrolytic salt splitting feasible on certain hydrometallurgical solutions. Meanwhile, environmental regulations have made the bulk disposal of salt solutions more difficult. In this paper, sodium sulfate salt splitting is examined from a cost perspective, compared to purchasing the reagents directly. Relative costs are estimated for several regions based on published electricity and reagent prices. The results show that salt splitting is economically favourable in some regions, and can be made more favourable by applying modifications to the traditional three-compartment desig