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By C. A. Young, J. D. Miller

Adsorption isotherms previously determined by in-situ Fourier transform infrared/internal reflection spectroscopy (FT-IR/IRS) for oleate adsorption at calcite and fluorite surfaces near pH 9 and at various temperatures are compared. Results indicate that, at both mineral surfaces, chemisorption occurs at equilibrium concentrations below approximately l x l0-5 M oleate while calcium dioleate surface precipitation occurs at higher equilibrium oleate concentrations. The extent of chemisorption at the calcite surface is 3 to 5 times less than that at the fluorite surface while the extent of calcium dioleate surface precipitation on calcite is nearly a magnitude larger than that on fluorite. However, for both minerals, surface precipitation decreases with increasing chemisorption. Contact angle measurements and flotation recoveries show the hydrophobicity of fluorite to be greater than that of calcite at each of the temperatures and oleate concentrations studied. Significant differences are noted only in the chemisorption region. Unlike calcite, the hydrophobicity of fluorite was sensitive to the presence of oxygen in the system. Multichannel Laser Raman Spectroscopy (MLRS) showed this behavior was caused by the double-bond reactivity of adjacent chemisorbed oleate molecules and subsequent formation of an epoxide/polyether complex at the fluorite surface. Such a reaction product could not be detected at the calcite surface. These differences in adsorption density, hydrophobicity, and polymerization behavior are discussed in terms of the intrinsic surface properties of the minerals.

Jan 1, 1999

By John R. FitzPatrick

The separation and purification of uranium from either nitric acid or hydrochloric acid media tan be accomplished by using either solvent extraction or ion-exchange. Over the past two years at Los Alamos, emerging programs are focused on recapturing the expertise required to do limited, small-quantity processing of enriched uranium. During this period of time, we have been investigating ion-exchange as a method for extraction/purification of uranium from acidic media. In addition, waste stream polishing is associated with this effort in order to achieve more complete removal of the uranium prior to recycle of the acid. Extraction chromatography has been demonstrated' to further polish the uranium from both nitric and hydrochloric acid media thus allowing for a more complete recovery of the actinide material and creation of less waste during the processing steps. We will discuss contact experiments for evaluation of eleven different resins for uranium removal from nitric acid, the evaluation (again by contact experiments) of uranium elution from the ion-exchange media by various chemicals, and small-scale experiments for the removal of 235U from nitric acid. Larger-scale (100-gram) flow experiments using depleted uranium, were done after the small-scale evaluation Of the selected resin. A discussion is also included concerning the shortcomings of the contact experiments and how the flow experiments were modified in order to overcome these problems. We will also discuss the application of ion-exchange for some specific process needs at Los Alamos Contact experiments were used to evaluate some commercially available solvent-impregnated resins in addition to evaluation of several resins of this type synthesized in our laboratory. These experiments' involved both nitric and hydrochloric acid media. The data from these experiments will be used to determine the column size and' amount of resin required to polish the waste stream produced by the ion-exchange process described above. Small-scale flow experiments will be described and data given on the mass balances achieved using this two step process. Future work for evaluation of new ion-exchange and solvent-impregnated resins as well as the search for new eluants will be discussed. Other future experiments for both processes, including large-scale experiments, will be discussed in detail.

Jan 1, 1996

By Peter Olubambi, Babatunde Obadele, Oluwagbenga Johnson

"The microstructure and corrosion behaviour of titanium carbide (TiC) reinforced duplex stainless steel matrix surface composites synthesized by laser melt injection technique was investigated. The surface melting operation was conducted using a 4.4 kW CW Nd:YAG laser with laser power of 1.5 kW, scanning speed of 0.4 to 1.0 m/min, beam size of 3 mm and argon shield gas flow rate of 4 L/min. The morphologies and microstructures of the coatings examined using field emission gun scanning electron microscope (FEGSEM) revealed homogeneous distribution of fine precipitates of TiC in the matrix, while X-ray diffraction (XRD) analysis confirm no phase change. TiC addition to the steels significantly increased hardness value to about 547 Hv0.1 but slightly decreased the corrosion resistance of the steels in 3.5% NaCl possibly due to the intergranular carbide coating that prevented chromium from forming continuous passive oxide layers.IntroductionComposite materials evolve from the idea of combining two basically dissimilar materials with different physical and mechanical properties to arrive at a product whose final properties are superior to those of the individual components [1]. Metal matrix composites (MMCs) are receiving much attention and are the focus of intense research and development worldwide for aerospace, automotive and other applications because of their excellent combination of ductility and toughness of the metallic matrix with high hardness and strength of carbides reinforced in the matrix [2]. Surface modification techniques such as laser, thermal spray, plasma spray, chemical vapour deposition have been use to fabricate MMCs. Laser melt injection (LMI) is a surface modification technique known since the 1980s [3] has been used to improve surface properties of metallic alloys such as aluminium, titanium and steels [4-6]. It involves the lateral injection of carbides, ceramics and cermets blown by a gas stream into a liquid metallic pool, created by laser irradiation of the top surface of the base material."

Jan 1, 2012

By Donghai Li, Cheng Pan, Xuewei Lv, Mei Liu, Enguang Guo

"Phosphorite is the main raw material for the production of phosphorus in chemical industry. More attentions have been drawn to the phosphorite concentrate beneficiated from low-grade phosphorite due to the decrease of high-grade phosphorite. For another, the agglomeration process is necessary for the phosphorite concentrate after beneficiation process. The mineralogy and sintering process of the phosphorite from Leshan, China were studied in this work. The result shows that the main phases in the phosphorite are fluorapatite (Ca3(P04)3F), hydroxylapatite (Cas(P04)3(0H)), quartz (Si02) and dolomite (CaMg(C03)2). The yield of the sinter increases with increasing the carbon dosage to 7%, and then decreases when it continuously increases. Similar regularities were found for the strength and the content of P20s of the sinter. The best strength of the sinter as well as its P205 content were discovered when the carbon dosage is 7%. Fluorapatite ((Ca5(P04)3)F) is the main phase in the sinter while fuggerite (Ca2MgSiz01) is the main binder phase.IntroductionPhosphorus is an important foundation industrial raw material of national defense industry, food industry and chemical industry, where it is used to produce red phosphorus, phosphonium hydroxide, phosphorus pentasulfide and phosphoric anhydride[l-2]."

Jan 1, 2013

By A. Block-Bolten

Copper concentrates from northern Peru contain large amounts of arsenic and antimony in the form of sulfosalts like enargite, tennantite and tetrahedrite. These impurities affect up to 30% of Peruvian copper production. Under the sponsorship of the Instituto Geologico Minero y Metalurgico in Lima a project to separate copper from arsenic without pollution of the environment is being carried out at the National University of Trujillo in Peru. The U.N.T. process is unique in the respect of using .low melting salts as solvents, and sulfides of metals with high cation potential as destructors of the complex sulfosalt molecules. Laboratory scale experiments have given encouraging results but interesting and difficult problems developed on scale-up. The process is pyro-hydrometal-lurgical and under certain circumstances its economics are promising.

Jan 1, 1981

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 Denise Cristina de O. Nascimento

Natural lignocellulosic fibers are increasingly being used as polymeric matrix composite reinforcement owing to economical and environmental advantages as renewable and biodegradable materials. Among these, the piassava fiber extracted from a palm tree native of South America stands as one of the most rigid with a potential to be used as composite reinforcement. Therefore, the present work investigates the notch toughness behavior, by Izod impact tests, of epoxy composites reinforced with up to 40 % in volume of continuous and aligned piassava fibers. It was found that the incorporation of piassava fibers results in significant increase in the impact energy of the composite. Scanning electron microscopy analysis showed that the nature of the piassava fiber interface with the epoxy matrix is the major responsible for the superior toughness of the composite.

Jan 1, 2009

By W. William Culver

James Douglas became known in the nineteenth century for two reasons fundamental to his mining career: (1) his experimental work with copper hydrometallurgy, and (2) his grasp of the idea that the quantity of copper ore matters more than the quality. On the first reason, there is a moment for any technology that’s critically important—when it moves from an area of scientific interest to one that companies are founded on. This paper examines the original 1869 Hunt and Douglas Copper Process in the context of science and engineering as they were in the 1860 and 1870s. It was a “humid” process, developed at Quebec’s Harvey Hill Mine. Chemically, the Hunt and Douglas vat leaching process succeeded, but not the original companies using it. On Douglas’ understanding of ore quality versus quantity, luck had it that the first company to field test the Hunt and Douglas Copper Process was in Chile. The Hunt and Douglas patent made that transition from experimental model to operational plant in 1870 when the Compañia de Minas de la Invernada was organized in Valparaíso. As a joint-stock company, Invernada spread the risk of investing in the revolutionary, but untested, Hunt and Douglas Process. The company brought Douglas to Chile as a consultant in 1871. His experience with hydrometallurgy, combined with what he learned about the copper business while in Chile, set him off on a career in metal mining that both surprised Douglas and made him wealthy.

By Uday Pal

In direct reduction processes for iron and steel making, significant amounts of Fe-C alloy droplets are generated and these remain suspended in relatively low FeO (around 5%) containing slags. Earlier workers have found that when the FeO content in the slag is <5%, the decarburization reaction becomes extremely slow (virtually ceases to occur) even though the alloy droplet contains a significant amount of carbons (2-3%). Understanding this rate controlling kinetic phenomena is crucial to designing an&apos; optimum direct steel making process. We studied decarburization of Fe-C particles by low FeO (<5%) containing CaO-SiO2A12O3 slags and found that by putting both the droplet and the slag in direct contact with an inert electronically conductive member that extends deep inside the slag bulk were able to quickly and completely decarburize the droplets. A detailed description and an explanation of the process will be presented.

Jan 1, 1995

By Z. W. Zhang, Songsong Xu, Jinhui Li, Yun Zou, Yu Zhao

High strength low alloy (HSLA) steels with high strength, high toughness, good corrosion resistance and weldability, can be widely used in shipbuilding, automobile, construction, bridging industry, etc. The microstructure evolution and mechanical properties can be influenced by thermomechanical processing. In this study, themomechanical processing is optimized to control the matrix microstructure and nano-scale precipitates in the matrix simultaneously. It is found that the low-temperature toughness and ductility of the steels are significantly the matrix microstructure during enhancing the strength by introducing the nano-scale precipitates. The effects of alloying elements on the microstructure evolution and nano-scale precipitation are also discussed.

Jan 1, 2016

By Ann M. Hagni

"Ceramic matrix composites are inorganic materials that are particularly resistant to heat and abrasion. A magnesia (MgO) and aluminum nitride (AlN) based composite is formed by exposing a magnesia preform to a metallic alloy block in a nitrogen atmosphere at 950°C. The metallic alloy, which is composed primarily of aluminum, is wicked into the preform. Aluminum nitride matrix is grown between MgO particles as the wicked metallic aluminum reacts with nitrogen. Unused metallic alloy, remnant metallic alloy (carcass), and composite produced after 8 hours, 50 hours, and 225 hours of processing are characterized mineralogically. Reflected light microscopy, transmitted light microscopy, scanning electron microscopy, energy dispersive spectroscopy, and X-ray diffraction techniques reveal that in addition to anhedral to euhedral AhNi, AbSbSr, and Al crystallizing in the metallic alloy carcass, AIN and (Al,Si)N have formed as well. Nitride rings and nodules in the carcass may hinder AIN growth in the composite. Fine-grained residual AhNi and AhShSr are dispersed throughout the composite matrix. The nitride matrix is composed of AIN and (Al,Si)N. Rim replacement of MgO by spine! occurs in the composite. Aluminum nitrides in the metallic carcass cathodoluminesce deep violet-blue, unlike non-luminescent AIN in the composite matrix. This distinction in cathodoluminescence suggests a different mode of formation for composite AIN than for carcass AIN. Phase interpretations and textural characterizations deduced from the implementation of sophisticated mineralogical techniques have contributed to the understanding, and will aid in the improvement, of MgO/ AlN-based ceramic matrix compositeprocessing."

Jan 1, 1999

By Baozhong Ma, Yonggang Wei, Shiwei Zhou, Bo Li, Chengyan Wang, Hua Wang

The effects of additives with Na2S, Na2SO4 and CaSO4 on phase transformation of nickel laterite ore in low-temperature reduction roasting process using carbon monoxide were investigated. The results showed that diffraction peaks of forsterite increased with increasing reduction temperature for 30min with the addition of 10wt% Na2SO4 and 50vol% CO, and diffraction peaks of forsterite increased with increasing the content of Na2SO4 at 900°C for 30min. Comparing the above three additives, phase transformation of nickel laterite ore were strongly influenced with the addition of 10 wt% Na2SO4 and 10 wt% Na2S. Calcium sulphide from the thermal decomposition of CaSO4 was carried out in the reaction product. SEM-EDS analysis result deduced that increasing the dosage of Na2SO4 from 10wt% to 15wt% could promote the polymerization of ferronickel and improve the grade of nickel in ferronickel.

Jan 1, 2015

By Huimin Lu, Liyuan Zhao, Zhijiang Gao

The aluminum matrix composite reinforced by graphene was successfully fabricated using high pressure torsion (HPT). With only 0.5wt% graphene, the grain size was reduced to 100nm while that of pure Al was about 500nm. The hardness of the composite increased from the center (64HV) to the edge (120HV) of the sample. Moreover, the tensile strength of this composite reached 197MPa, while that of pure Al was 157MPa. The enhancement in mechanical properties was induced by grain refinement, load transfer from the matrix to the reinforcement and dislocations piled up at the grain boundaries.

Jan 1, 2015

By Sang-Beom Lee

For thermodynamic prediction, the deoxidation equilibrium of aluminum in Fe-36%Ni alloy was studied with a cold crucible under Ar gas atmosphere at 1773K. For the deoxidation reaction in liquid Fe-36%Ni base, i.e.: A12O3(s) = 2A1 + 3O The interaction parameters and the equilibrium constant between aluminum and oxygen in liquid Fe-36%Ni alloy are given in the following: eo Al = -3.8, roA1=0.9, eAl° = -6.4, rAl° = 700, rAIAIo = 3.1, roA1o = 833 within the composition range of [Al] < 1 mass%. The temperature dependence of the equilibrium constant was obtained in the range of 1773K < T < 1973K by using reported data and present results as follows: log KAo= 0.58-24463.7 / T The deoxidation equilibrium with aluminum in Fe-36%Ni could be thermodynamically well described in the range up [Al] < 1 mass% with first and second order interaction parameters as well as the equilibrium constant determined in this study.

Jan 1, 2002

By K. Potluri, S. Akella, S. Bhansali

"This paper presents the design and angular strength analysis of microneedles for use as a transdermal interface for drug delivery, fluid analysis and sampling etc. Microneedles of different dimensions were designed and fabricated using various materials viz. Si02, OxideNitride- Oxide (O-N-0). The design, modeling and analysis was done using the Finite Element Analysis (FEA) software ANSYS™ 6.1. Angular strength analysis of the microneedles was done using angular loading in ANSYS™, with the corresponding inaterial property settings. Using the force-displacement settings, forces of magnitudes in the range of 10 mN - 25 mN were applied on the microneedles at loading angles ranging from 30° to 90° was applied on needles. Square and circular shaped microneedles were modeled and the displacements and stresses generated were studied to characterize the angular strength of the microneedles. The buckling and force-displacement analyses show that O-N-O microneedles are more strong and robust as compared to needles of other materials. The analysis shows that while circular microneedles have uniform stress distribution, square microneedles have low stresses concentrated along the edges.INTRODUCTIONIn modem clinical and biomedical applications, drug delivery is done either by oral administration or by hypodermic injection. Hypodermic injection of drugs using needles is often painful. Hence, transdermal drug delivery techniques are increasingly being sought out as an alternative. In transdermal drug delivery the needles puncture the Stratum comeurn - the outermost layer of the human skin. The advantage of transdermal drug delivery (or transdermal measurement) technique, is that it reduces pain and tissue trauma."

Jan 1, 2004

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 Corby G. Anderson

Hydrometallurgical technology for the pretreatment of refractory gold concentrates has been developed at Sunshine Mining and Refining Company. It employs a patented nitrous-sulfuric acid pressure leaching process which&apos; was proven industrially at the Sunshine refinery. Additionally, pretreatment for removal of antimony and some other impurities is done with alkaline sulfide leaching. This paper will discuss the successful application of these two technologies for pretreatment of a refractory gold concentrate prior to CIL gold recovery. A complex gold concentrate composed of pyrite, arsenopyrite and stibnite was tested. Results of antimony leaching in alkaline sulfide media will be discussed including some details of a novel and selective recovery method for gold leached by polysulfide or thiosulfate" Also, the factors important in and the results of the application of nitrogen species catalyzed pressure leaching to refractory gold concentrates will be detailed.

Jan 1, 1996

By Yang Cui

The partition ratios of lead and antimony between liquid copper and MgO saturated Cu2O-CaO-SiO2 flux and their removal rate by using CuCl-based flux were measured between 1423 K and 1573 K. For Cu2O-CaO-MgOsatd. system, the partition ratio of Pb was not affected by the CaO content at 1573 K, while that of Sb increased with increasing CaO content. The maximum value was 160 at the CaO content of 15.4 mass%. For Cu2O-CaO-SiO2-MgOsatd. system, two liquid phases of calcium silicate rich phase and Cu2O rich phase were observed at 1573 K. The partition ratios of Pb and Sb between calcium silicate phase and liquid copper depended on the (mass%CaO)/(mass%SiO2) ratio. When the (mass%CaO)/(mass%SiO2) ratio increased, the partition ratio of Pb decreased and that of Sb increased. For CuCl flux, the removal of Pb from liquid copper at 1473 K was possible, and a relatively low concentration could be reached. Moreover, most of lead as metal chloride vaporized from flux. For the removal of antimony from liquid copper at 1423 K, it was difficult by CuCl flux, and the removal ratio was approximately 20% for 75 minutes. However, the addition of CaO or Na2CO3 to CuCl flux was relatively effective to remove antimony, and the concentration of antimony reached a relatively low value after 15 minutes by using CuCl-CaO or CuCl-Na2CO3fluxes. Moreover, a small part of antimony as chloride vaporized from flux.

Jan 1, 2006

By E. Morrice

Solubility of yttrium oxide (Y203) in fluoride melts was experimentally measured in the temperature range of 998 to 1273 K and, YF3 composition in LiF.YF3 melts varying from 20 to 50 mole pct using a graphite crucible in an argon atmosphere. Solubility of oxide in the melt was found to increase with increasing temperature and YF3 composition in the melt. An expression for in XY2O3 as a function of temperature for several melts was deduced. The calculated activity coefficients of Y2O3 in the melts exhibited a negative deviation from Raoult&apos;s law.

Jan 1, 1989

By Tianzu Yang, Weifeng Liu, Lin Chen, Deyu Wang

"Due to the gradual exhaustion of easily extractive gold ores, it is vital to make efficient use of refractory gold ores which hold 30% gold storage of the world. However, the disadvantage of current processing technologies for refractory gold ores consists of severe pollution, low gold extraction ratio, high investment, etc, thus great research interests were attracted during recent years. This article provides an overview of the distribution and categories of the refractory gold ores in the world. The state of art in processing refractory gold ores by pyrometallurgy, hydrometallurgy and biometallurgy techniques and their industrial applications are highlighted. Potential environmental conservative techniques for efficient gold extraction are also reviewed.IntroductionResources of Refractory Gold OresAs easily extractive gold ores are going to be exhausted with the large scale mining nowadays, refractory gold ores are becoming more and more important. Gold in the refractory gold ore cannot be fully extracted using conventional method (cyanidation) even with fine grinding. The amount of gold in the refractory gold ores is about 1500~2000t in China, which occupies 30~40% of the total gold storage [1]. Therefore, it is vital to make efficient use of refractory gold ores."

Jan 1, 2013