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By Ping Long, Bin Yang, Jian Wu, Xiumin Chen, Wenli Zhang

In this study, the analysis method of trace element in pure indium using glow discharge mass spectrometry (GD-MS) has been established by correcting the analysis result, which was obtained from non-standard quantitative method of GD-MS. The effect of instrument operating parameters, the resolution and isotopes and the pre-sputtering time on the determination results were investigated respectively. The optimized operating parameters of the instrument were obtained as follows: the discharge current was 37.5mA and discharge airflow was 475ml/min. Mass spectral interferences have been eliminated using selected resolution and isotope. The pre-sputtering time was 30 min. 4 trace elements in two pure samples were determined for 6 times. The RSD were less than 20%. The content of trace elements in indium samples was determined by GD-MS and Chemical Analysis Method of Indium which is tested by inductively coupled plasma atomic emission spectrometry, respectively. The results were consistent with each other.

Jan 1, 2016

By R. Cameron

The growing use and acceptance of electric vehicles (EV), as evidenced by the record sales of over 750 thousand vehicles in 2016 and a current global EV stock of 2 million vehicles, is putting pressure on sourcing raw materials such as cobalt, and to a lesser extent, nickel. Global supply is poorly diversified, with 50– 60% of global cobalt production sourced solely from the Democratic Republic of Congo (DRC). One potential source for cobalt and nickel are low-grade nickeliferous pyrrhotite tailings, of which 50–100 million tonnes are present in the Sudbury area alone. This paper presents the extraction of cobalt and nickel from this material using a combination of flotation and bioleaching technologies. The findings of a high-level techno-economic analysis of the proposed processing flowsheet are presented.

By Liangying Wen, Xuewei Lv, Yuelin Qin, Feng Zhu, Guibao Qiu, Chenguang Bai, Meilong Hu, Shengfu Zhang

"The COREX process is the first reduction ironmaking technology with coal and pure oxygen to get high quality hot metal, which consumes a lot of high quality lump coal and some coke. In order to increase the utilization of fine coal, reduce coke consumption and enhance the competitiveness of the technology, the combustion behavior of pulverized coal injection in melter gasifier is studied experimentally. The results show that the combustion rate of PCI increases with the increase of temperature. And the combustion rate increases with decreasing coal particle size. Compared bituminous coal with anthracite, the former’s burning ratio is higher than the latter in the same granularity. The combustion effect is remarkable when coal blend of bituminous coal and anthracite with the smaller particle size is pulverized in COREX process.IntroductionThe COREX process is the first reduction ironmaking technology with raw coal and pure oxygen to get high quality hot metal, which consumes a lot of high quality lump coal [1-3]. However, the proportion of lump coal in raw coal is very small, and it is avoidless to produce fine coal because of mechanical coal cutter and storage and transportation process, so it is important to resolve utilization of fine coal in COREX ironmaking process in order to energy conservation and reduce the cost of hot metal [4]. Currently, Coal briquetting technology is adopted to utilization of fine coal in COREX process [5], but coal briquetting system has high investment cost and requires feasible adhesive agent. The pulverized coal injection (PCI) into a blast furnace is being used on a global scale to improve the stability and reduce the cost of blast furnace operations [6]. The successful development of PCI in blast furnace is contributed to pulverized coal in COREX melter gasifier. However, it is different in PCI process between COREX melter gasifier and blast furnace, and the differences are as follows: firstly, The air is injected into blast furnace, which temperature is about 1200 ?, but in COREX melter gasifier the normal temperature oxygen is blasted, so PCI in blast furnace begin burning in blowpipe, but the combustion of PCI in COREX melter gasifier is only in raceway. Secondly, the racway of COREX is smaller than that of blast furnace of the same size. So, the combustion behavior of PCI is complex in COREX melter gasifier, which is not use for reference."

Jan 1, 2012

By W. B. Carter, A. T. Hunt, G. W. Book

"Combustion Chemical Vapor Deposition (CCVDSM ), an open air, flame assisted CVD process, is under development. The CCVD process produces non-line-of-sight, epitaxial deposition. Materials deposited include YBa2Cu3Ox' Y2BaCuOx, BaTiO3, Y2FesOI2, ZrO2, yttria stabilized ZrO2 (YSZ), partially (yttria) stabilized ZrO2 (PSZ), and amorphous silica. Two modifications of the CCVD process are being studied. Liquid fuel CCVD deposition, involves the combustion of an organic solvent that contains dissolved reagents carrying the desired coating cations. Gaseous fuel CCVD deposition uses a flammable gas as fuel. A non-flammable solution containing dissolved reagents is either aspirated into the flame or mixed with the fuel gas as an aerosol prior to its combustion. Substrates to be coated are held near the flames' ends.IntroductionThin films and coatings can be deposited using a wide variety of techniques including chemical vapor deposition (CVD). CVD is ""a materials synthesis process whereby constituents of the vapor phase react chemically near or on a substrate surface to form a solid product.""lIn conventional CVD processing, gases carrying coating constituents flow into a reaction vessel where deposition occurs onto a heated substrate. The deposition process is often conducted at reduced pressure. Both cold and hot wall reaction chambers are used. Heat can be provided by a resistance furnace, rf induction, or high-intensity radiation lamps. Plasma, microwave, photo, laser, RF, and electron-enhanced CVD processes have been developed. The necessity of using a reaction vessel limits the substrate size and affects coating economics. Although most CVD depositions are performed as batch processes, continuous deposition can be accomplished with the use of appropriate hardware.The chemical vapor deposition of thin, dense oxide films has been accomplished in the open atmosphere with a flame assisted process. The process is called combustion chemical vapor deposition (CCVDSM).2 Two modifications of the CCVD process have been developed. The liquid fuel CCVD process involves the combustion of an organic solvent in which reagents (containing the coating cations) are dissolved. The gaseous fuel CCVD process uses a flammable gas as fuel. In this modification, a non-flammable solution containing dissolved reagents is either aspirated into the flame or mixed with the fuel gas as an aerosol of small droplets prior to its combustion. Substrates to be coated are held near the flames' ends."

Jan 1, 1994

By H. L. Ludtke

Microlaminate composites were fabricated by electron-beam physical vapor deposition. The microlaminates consisted of five layers, each 2 to 4 pm thick, and were composed of either pure metal layers (Cu-Ag), or alternated between metal and intermetallic layers (Nb(Al)- Nb3Al). The microlaminates were heat treated in an Ar atmosphere for 2 to 12 hours, at temperatures of 600°C for the Cu-Ag and 1000°C to 1200°C for the Nb(Al)-NbsAl. Microlaminates were examined after deposition and after heat treatment by scanning electron microscopy and energy dispersive x-ray spectrometry. The effects of heat treatment on the morphological stability of these composites will be described.

Jan 1, 1999

By Carlos M. Fontes Vieira, Ruben J. Sanchez Rodriguez, Carlos E. Gomes Ribeiro

"In this study we attempted to model a response surface for the apparent dry density of ternary blends of calcitic marble particles. The crushed marble was divided into three granulometric ranges. Simplex network methodology was used to determine the mathematical relation between granulometric ranges and apparent dry density (ADD) of particle mixtures. A highly significant regression was obtained and the simplex network methodology proved to be able to predict high packing particle compositions.IntroductionProblems with packing and expected porosity of particles are common and widely recognized to be important in terms of both fundamental physics and engineering applications. For example, densification of a powder mass is important in the shaping of solids in ceramics, powder metallurgy or composite synthesis; chemical processes such as solid-liquid separation (sedimentation, thickening and filtration), raw material handling (stockpiling, blending, drying, storage and transportation) and pyrometallurgical processes (agglomeration, coke making, ore sintering, blast furnace iron making and new iron making processes) [1,2].Many factors can affect particle packing, but in practice, there are three main factors: (dimensionless) particle size distribution, particle shape and absolute particle size [2].Geometrical and practical methods were developed to predict properties in mixtures. Zou, Gan and Yu [2] present a paper treating a prediction of the porosity of multi-component mixtures of cohesive (fine) and non-cohesive (coarse) particles. Bahiense et al. [3,4] used a simplex network to determine a mathematical model for obtain the optimal compositions between aggregates to a greater packing of a ternary particles mixture. Despite these techniques for predicting particle packing, some studies in particulate composites production don't present clear criteria for choice of particle distribution [5,6]. As the best particle packaging depends on the size, distribution and shape of these particles, individual models can be constructed for specific combinations of these factors."

Jan 1, 2014

By M. Pineau, G. A. Monteith, M. Laliberte, G. Houlachi

Conventional physico-chemical treatment methods, either hydroxide or sulfide precipitation, can hardly achieve a high removal of selenium from the liquid effluents which can be generated in some metallurgical operations. In weak acid solutions, selenium exists mainly as anionic species (selenite Se03-2 and selenate SeCV2) which, therefore, cannot precipitate as metal hydroxide or metal sulfide compounds. At the same time, neither selenite nor selenate form stable precipitates with the common cations (Ca, Mg, Fe, etc.) that are typically used in water treatment. At Noranda Inc., CEZinc Division in Valleyfield, Canada, the introduction of new discharge requirements for effluent toxicity initiated a R&D program which resulted in the full-scale implementation of a new treatment method for selenium removal. The goal of this paper is to present this new method which is now being patented by CEZinc. The process chemistry will be presented along with pilot-scale developments and full-scale operational results.

Jan 1, 2000

By R. K. F. Lam

Unacceptable levels of impurity were noted in high purity chromium melting. Analysis of recent melting data determined that oxygen content in chromium is the critical parameter. Thermodynamics studies identify zirconia to be the most stable oxide in the presence of liquid chromium, followed by alumina and silica. Iron oxide reacts readily with liquid Cr. A certain degree of chemical reaction between liquid chromium and oxides does occur, contamination by the crucible is therefore unavoidable. Equilibrium constants indicate that a chromium oxide addition decreases 'ceramic dissolution and reduces impurity contamination. Safe operating conditions with oxygen content between 1190 ppm and 2500 ppm were identified. Additions of chromium oxide (Cr2O3) of 161 grams and 264 grams to liquid chromium yielded acceptable levels of impurity, and oxygen content was respectively increased to 1624 ppm and 2 179 ppm. A new process of melting high purity chromium with chromium oxide addition for controlling the activity of Cr2O3 is recommended.

Jan 1, 1997

By Ahmad Umar

A variety of ZnO nanostructures such as sea-urchin-like structures composed of nanowires and nanorods, nanocombs, nano/micro spheres and cages, star-shaped ZnO nanostructures, flower-shaped nanostructures, needle-like nanostructures etc. have been synthesized applying two different fabrication techniques i.e. thermal evaporation and cyclic feeding chemical vapor deposition techniques at different reaction parameters such as reaction temperature, growth period, reactant concentrations, types of source material and substrates etc. It was observed from the experiments that the morphologies of the grown structures were highly influenced by the reaction parameters and fabrication techniques and specific morphology can be obtained at particular reaction parameters in a specific synthetic procedure. Extensive morphological investigations of the obtained products demonstrate that the grown structures are single crystalline and having a wurtzite hexagonal phase. Room-temperature photoluminescence spectra of all the deposited products exhibited good optical properties. Finally, the growth process of the fabricated structures were proposed and discussed in detail.

Jan 1, 2006

By Ryosuke Matsuoka

Keywords: Tantalum capacitor, Scrap, Recovery, Titanium, Chlorination A recycling process for tantalum from capacitor scraps using an oxidation process followed by mechanical separation and chemical treatment was investigated. This study demonstrates that sintered tantalum electrodes inside the capacitor scraps can be mechanically collected after the oxidation of the scraps in air, and high-purity tantalum oxide powder (Ta2O5) was efficiently recovered after chemical treatment. By reducing the Ta2O5 obtained through magnesiothermic reduction, tantalum powder with 99 mass-% purity was obtained. Using the chlorination for tantalum recovery was also investigated, and the tantalum or tantalum compounds were reacted with chloride wastes such as FeClx. It was found that tantalum was effectively separated and purified when tantalum powder is reacted with FeClx at 1100 K under an argon atmosphere. This recycling process utilizing chloride scrap has now been extended to other reactive metals such as titanium.

Jan 1, 2004

By Andreas Dietrich

Laser off-gas measurement of CO, O2 and temperature has been carried online in EAFs. A visualization screen shows the values of CO and Oxygen and temperature for the entire heat, and includes the status of furnace equipment. The historical data of the heats are stored such that the furnace performance can be evaluated and optimized. A short comparison between laser based and conventional systems has been carried out related to speed, influence of dust, water, pressure, protection for bag house explosions. A high water and/or dust content in the sample does not represent a problem for this type of system. The measurement method works without interruption even under worst conditions such as dirty scrap, carbon injection etc. The installation was developed in conjunction with Marienhuette, Graz. They are 100% scrap based with a tap to tap time of ca. 46 min. Keywords: Laser Measurement, Off Gas, CO, O2, Temperature

Jan 1, 2003

By B. M. Satish

The aim of the present work is to study the effect of annealing on the vibration damping capacity of high-chromium (16%) ferromagnetic steel. The alloys were prepared from raw materials of 99.9% purity melted in a high frequency induction furnace under high vacuum. The samples were heat-treated in vacuum at various temperatures (800 to 1200°C) for 1 hour followed by slow cooling (120°C/h). The inverted torsional pendulum method was used to evaluate the vibration damping capacity. The results indicated that the vibration damping capacity of the alloys is influenced by annealing and there exists a critical annealing temperature after 1000°C. The damping capacity increases quickly below the critical temperature since the magnetic domains move more easily.

Jan 1, 2009

By A. Kiziltas, D. J. Gardner, C. W. Mcllwraith, J. W. Bridge, M. L. Peterson

"Dynamic mechanical thermal analysis (DMTA) tests were conducted on high-oil content, paraffin-based wax used in wax-coated granular composites. These composites make up the surface of synthetic Thoroughbred horse racetracks used in North America. The modulus and damping response from the DMTA tests were correlated with the dynamic triaxial shear strength response of the bulk track material taken at two different operational temperatures and at four strain rates. The purpose of these tests is to understand the mechanisms of shear strengthening of the bulk track material as the wax is heated through the first crystalline solid to liquid nominal transition temperature. Previous work using differential scanning calorimetry confirmed that under common operational surface temperatures, the wax coatings undergo distinct thermal transitions. The resulting increase in triaxial shear strength values affects the consistency of the racetrack which, in turn, can potentially affect Thoroughbred racing performance and safety of the track surface.IntroductionSynthetic granular composite materials are being used in nine Thoroughbred horse racetracks in the United States as well as in other tracks around the world. In one case, their use was mandated by the state of California in 2007 due to testimony that these tracks were significantly safer than traditional dirt tracks [1]. Several synthetic tracks have shown substantial reductions in injuries since switching to synthetics; one California track showed a 75% reduction in catastrophic horse injuries during the first year as compared to the previous year racing on a dirt track [2]. The composition of the tracks in the U.S. generally consist of silica sand (>70%), polymer fibers (<5%), and rubber particles (0-15%) all coated with a paraffin-based, high oil content wax [3, 4]. In a recent study of several synthetic racetracks, to include the track location in this study, the oil content ranged from 34 to over 44% by mass [5]."

Jan 1, 2011

By M. F. Chambers

Neodymium metal was electrowon from a molten-chloride electrolyte at 650° C using a molten-metal cathode. A 50 mol pct NdC13-50 mol pct KC1 mixture served as the electrolyte. Binary metal alloys of &apos;Mg with Zn and Mg with Cd were used as molten cathodes. Under the best conditions, current efficiencies were 90 pct with a Mg-Zn cathode and 80 pct with a Mg-Cd cathode. Vacuum distillation was performed at 1,100° C for 30 min under a vacuum of 10-3 to separate the cathode metals from the neodymium. Neodymium metal of 99.9+ pct purity was recovered from the Mg-Cd alloy cathode. Almost 2 pct zinc remained in the neodymium recovered from the Mg-Zn alloy.

Jan 1, 1989

By B. C. Tripathy

The effects of alkali metal ions Li+, Na+, K+and transition metal ions Cr3+ and Mo6+ on the cathodic current efficiency, deposit quality, crystallographic orientations, deposit morphology and polarisation behaviour of the cathode during nickel electrocrystallisation on stainless steel substrate from aqueous sulphate solutions containing boric acid were investigated. The alkali metal ions had virtually no effect on the cathodic current efficiency, deposit quality, crystallographic orientations, deposit morphology and cathodic polarisation. On the other hand, there were significant variations in the current efficiency and deposit characteristics when Cr3+or Mo6+ were present in the electrolyte. Current efficiency decreased by more than 10% even at lower concentrations (> 100 mg/L). Similarly purity of the deposits was affected by the presence of either of the metal ions. In the presence of Cr3+, there was progressive shifting of the nucleation potential of nickel towards more negative values, whereas, in the case of Mo6+the nucleation potential shifted initially towards positive values in the concentration range 2-40 mg/L, but then towards negative values when its concentration exceeded 40 mg/L.

Jan 1, 2003

By Xia Hong-ying, Peng Jin-hui, Zheng Zhao-qiang, Zhang Li-bo

"Preparation of activated carbon from the walnut shell by microwave assisted steam activation was studied. Influences of the three parameters, activation temperature, activation duration and steam flow rate on the adsorption capacity and yield of walnut shell activated carbon(WSAC) were investigated,optimization process was obtained by the Response Surface Methodology (RSM). The optimum preparation conditions were as follows: activation temperature of 980°C, activation duration of 41 min and steam flow rate of 1.66 ml/min. The optimum conditions resulted in an activation carbon with an iodine number of 1025 mg/g and a yield of 52.17%, while the BET surface area, total pore volume and average pore diameter of WSAC were 1328m2/g, 0.72ml/g and 2.2nm respectively. The study supported the potentiality of comprehensive utilization ofWalnut shell and the benefits of the microwave heating.IntroductionActivated carbons are one of the most important adsorbent materials in modern society because of its abundantly developed pore structure, strong adsorption ability, high surface area and thermo stability. They have extensive application in many industries fields which include gas purification [1], catalyst supports [2] and other pollutants [3]. However, in recent years, the industrial production of activated carbon is facing the problem of raw material scarcity and high cost, which limit to be widely used. Therefore, the selection of an appropriate precursor plays an important role and it has become hot sport to seek cheap raw material to lower preparation cost. As a kind of reproducible resource, the waste from agriculture and forestry is a high-grade raw material for preparing activated carbon due to is high carbon content, such as palm shell [4], rice hull [5], and coconut shell [6]. At present Walnut shell is widely accepted to be a renewable source of biomass. According to statistics, there is more than 1000,000 tonnes of walnut shells are produced in China annually [7]. As a good precursor for activated carbon production, Walnut shell is a major agricultural waste, to make better use of the cheap and abundant agricultural waste, it is proposed for activated carbon production."

Jan 1, 2014

By W. G. Davenport

Chapters 7,8and 9 calculated three combinations of: blast composition (mass% O2, mass% N2) oil quantity per tonne of concentrate blast temperature that will steadily produce molten 65% Cu matte from pure chalcopyrite-concentrate. The combinations are:

Jan 1, 2001

By Anxiang Wang, Kunhua Wu, Yifu Li, Junjie Xu, Yongnian Dai, Bin Yang, Lingxin Kong

In this study, the saturated vapor pressures of tin (Sn) and antimony (Sb), the separation coefficient and the vapor-liquid phase equilibrium of Sn-Sb alloy were theoretically analyzed, which demonstrate that it is possible to separate Sn and Sb by vacuum distillation. The process parameters of vacuum distillation, including the distillation temperature, distillation time and alloy mass (thickness of raw materials) on the direct yield of Sn and the content of Sn in liquid phase were investigated by using single factor experiments. The preliminary results show that the direct yield and the content of Sn are 98.77 wt.% and 96.01% with the optimized distillation conditions of a distillation temperature of 1473 K, a distillation t ime for 45 min and a Sn-Sb alloy mass of 125 g ( thickness o f 8 mm). The distillation parameters in the study provide effective and convenient conditions on separation of Sn-Sb alloy.

Jan 1, 2016

By K. Koike, N. Masuko, Y. Takasaki

At the Zinc & Lead'95 symposium, one of the authors presented several modifications of Pb-Ag-Ca alloy anodes for the zinc electrowinning process, and also, the behavior of some organic additives in the electrolyte. In this study, the mechanical properties of the electrode materials composed by Pb-0.5 wt% Ag-(0~0.8) wt% Ca were studied by the tensile and Vickers hardness methods. Furthermore, experimental research on the influence of rolling and annealing treatments on the electrolytic behavior and mechanical properties of these alloys was carried out. The tensile strengths of the annealed Pb-0.5 wt% Ag-(0.1-0.8) wt% Ca alloys were the same or higher than those of the as-cast Pb-0.9 wt% Ag alloy. The anode potential using the as-cast Pb-0.5 wt% Ag-0.6 wt% Ca alloy decreased compared to the as-cast Pb-0.9 wt% Ag alloy. Moreover, the annealed Pb-0.5 wt% Ag - 0.6 wt% Ca anode after rolling showed a lower anode potential than the as-cast Pb-0.5 wt% Ag - 0.6 wt% Ca anode.

Jan 1, 2000

By K. Prashant Sarswat

Isotopes are critical to a variety of applications including physical science analyses, biology, medicine, pharmaceuticals, and national security. In most cases isotopes must be relatively pure or highly enriched before they become useful. Current isotope separation technologies are relatively inefficient, capital and labor intensive, and often produced by a limited number of suppliers. In the category of isotopes, lithium is among other important candidates. Lithium is found naturally in two isotopes, 6Li which accounts for 7.5% of all lithium, and 7Li which makes up the balance of 92.5%. Each of these isotopes is important to the nuclear industry. 7Li is often used in the form of lithium hydroxide which is used to control pH in pressurized water reactors. The current supply of 7Li is based mostly outside of the United States, and its long-term supply is uncertain. Apart from supply issues, the use of mercury for 7Li separation is also a concern in commercial processing using the most common and efficient approach [1–3]. Hence, a reliable, environmentally friendly, and efficient technique is needed to produce 7Li. In this line of investigations, the authors used a two-compartment system and significant separation was achieved. In this piece of research, some preliminary results are presented including cell design and actual isotope ratio after enrichment. Applying an electro-potential across two electrodes can be used to drive electromigration of Li isotopes. The electromigration is in addition to normal diffusion. Note that 6Li diffuses faster and hence there will be a lowering of the 6Li concentration near the positively charged electrode and an enhancement in 6Li near the negative electrode during the separation process. Similarly, 7Li will be more prevalent near the positive electrode and less prevalent near the negative electrode during the initial separation stage [1].