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By Jun Miao, Kang Liu, Jilai Xue, Jun Zhu

CO2 emissions must be reduced by at least 50 % by 2050, and hence the technical solutions to capture and convert CO2 into value–added products should be considered. A Cobalt(III) Schiff base complex (Salen–Co(III)) has been investigated as a catalyst for synthesis of cyclic carbonate from CO2 and epichlorohydrin(ECH) with tetrabutylammonium bromide (TBAB) as co–catalyst. To recover Salen–Co(III) for the next cycling operation, it was immobilized onto zeolite 13X through excessive impregnation method. The immobilized catalyst was characterized using XRD, SEM, BET and ICP–AES techniques. Catalytic tests showed that yield of cyclic carbonate reached 90 % using 0.5 mol % Salen–Co(III) at ambient conditions. The immobilized Salen–Co(III) exhibited better catalytic activity than the homogenous one when used at the first cycle, but the yield decreased by some 20 % after five cycles.

Jan 1, 2015

By O. A. Bascur

Applying the latest information technologies in mining and metallurgical complexes has become a serious challenge to management and technical teams. Emerging component design is changing the way the user relates to the desktop. Connectivity between mining and metallurgical process operations and their business systems has become a reality. Expanded use of plant information on the desktop is a standard tool for revenue improvement, cost reduction and adherence to production constraints. The industrial component desktop support access to information for continuous improvement and innovation by staff personnel and engineers. Collaboration between groups enables the implementation of an overall process effectiveness index based on losses due to equipment availability, production recovery and quality rate. The integration of information from mining, mineral processing and metallurgical performance monitoring increases production efficiency, even when many elements cannot be measured directly. Three case studies of large mining/metallurgical complexes are highlighted.

Jan 1, 1999

By Hiroyuki Sano, Chikabumi Yamauchi, Mitsuru Tanahashi, Toshiharu Fujisawa, Shin-ya Iwahori

"Pyrometallurgical process using Cu2O-based slag was proposed as a recycling process for copper scrap. However, it is difficult to remove nickel from copper by oxidative refining. Therefore, it is necessary to reduce the concentration of nickel in copper before the oxidative refining. In the present work, the copper enrichment stage in this recycling process, where copper scrap melt is separated into the Fe-C-Cu melt and the molten copper, was taken up and the compositions of both melts were measured. Based on the above results, the distribution ratios of nickel between the Fe-C-Cu melt and the molten copper were calculated. Furthermore, the optimum condition of copper enrichment stage was discussed from the viewpoint of nickel removal and copper recovery. The possibility of recovering 4N-purity copper by using this recycling process was confirmed.IntroductionRecycling is well known as a method for saving resources and reducing environmental damage. More than 99% of copper is used in metallic form - as metal or copper alloys[l]. High-grade copper scrap is directly re-melted and reused, while low-grade copper scrap is transported to copper smelters to be pyrorefined and electrorefined. Nevertheless, a great amount of copper is being stockpiled in the cities and should be recycled in the near future. At that time, the current recycling process will face new problems due to the increases in the recycling rate to the smelters. This includes insufficient combustion heat to melt copper scrap and ·almost no benefit in electrorefining because the scrap does not contain gold and silver. Thus, an alternative pyrometallurgical method for copper scrap refining will be required."

Jan 1, 2000

By Singareddy R. Reddy, Ramana G. Reddy

"The Margules equation is used for interpreting excess Gibbs energy of several ternary systems. An expression for the activity coefficient of a dilute solute, 2(oxygen), in a binary solvent 1-3 is derived. It is used to calculate the logarithmic activity coefficient of oxygen in Pb-O-Gu, Pb-O-Bi, AgO- Sn, Pb-O-Sn and Ag-O-Pb metallic systems. Self interaction parameter of the solute is derived from the partial Gibbs energy of solute using constant compositional path. The derived equation is used successfully to deduce the self interaction parameter of oxygen in Pb-O-Gu and Pb-O-Bi metallic systems. The predicted thermodynamic parameter data i.e activity coefficient and self-interaction parameters are in an excellent agreement with the experimental data and also our predictions are far more accurate than the predictions made by other models.1 IntroductionThe nature of solute interactions such as oxygen, nitrogen and sulfur with the metallic solutions are important for a number of chemical and metallurgical processes. Several theories [1-23] have been developed to evaluate fundamental thermodynamic properties of solutes constituting two elements. The activity of solutes has been calculated using statisticalor quasi- chemical approach.Wagner's [4] Ideal Solvent Model is based on one energy parameter to describe the compositional dependencies of the activity coefficient of nonmetallic solutes such as oxygen in binary metallic solutions. This model depends on a constant energy of interaction for the exchange of atoms from the coordination shell of an oxygen atom to the shell of an interstitial site and cannot account for properties of strongly interacting systems [4]. Therefore, several attempts have been made to improve the Wagner's model for the strongly interacting systems. [10-16]."

Jan 1, 1996

By J. H. Puffer

The copper mineralization of the Mesozoic Passaic Formation of New Jersey is typical of copper deposits in eastern North American Mesozoic sediments. Most such deposits are located at the base of the first of several basalt flows that are interbedded with continental, red-bed sediments. The copper mineralization is similar in most respects to that of the Keweenawan Basalts of the Lake Superior area. The first basaltic flow units of the eastern North American Mesozoic basins, and the Keweenawan Basalts, are continental quartz tholeiites of similar chemical composition and copper contents. The copper minerals and associated zeolite facies metamorphic mineral assemblages of these two rock units are also approximately the same. Stoiber and Davidson (1959) suggested that Keweenawan copper was mobilized and concentrated during metamorphism. The evidence pertaining to the Mesozoic copper deposits of New Jersey is consistent with such an interpretation and also with DeVore's (1955) suggestion that ore fluids commonly arise as a result of the mobility of metals under metamorphic conditions. There is additional evidence that final metamorphic concentration of Mesozoic copper was preceded by an initial stage of hydrothermal precipitation related to fluids emitted by basaltic magma.

Jan 1, 1987

By Maria D. Salazar-Villalpando, Anthony Cugini, Bryan Reyes

"The electrochemical reduction of CO2 was performed in a laboratory-made, divided Htype cell. A copper electrode was used as the cathode. An Aldrich Nafion 117-type ion exchange membrane (0.18mm thickness) was used as the diaphragm. NaHCO3 and KHCO3 were studied as the catholytes. Hydrogen evolution from water reduction and products from CO2 electrochemical conversion were recorded. Higher CO2 reduction enhancement was observed by KHCO3 as compared to NaHCO3. The main conclusion of this work is that in fact CO2 can be electrochemically reduced with copper electrodes.1.-INTRODUCTIONThe direct electrochemical reduction of CO2 may allow for a simple process and, by avoiding high temperature reactors, would enable the process production rate to be quickly varied to follow the time of day availability of surplus electricity [1]. Temperature has a major effect on the electrochemical conversion of CO2 since its solubility increases when temperature decreases [2]. The electrical potential applied to the electrochemical reacting system will have an influence on the product distribution, as well. For example, a narrow potential range during cyclo-voltagraphic studies will determine the detection of a lower number of products. A recommended potential range to study the electrochemical reduction of CO2 is -2V to 2V. Moreover, the reaction rate on the electrode is governed by various processes, such as the kinetics of electron transfer, adsorption/desorption at the electrode surface, and diffusion of CO2 to the Cu electrode. The availability of active species, CO2 for electro-reduction, is extremely low at the vicinity of the electrode surface and it seriously interferes with the rate of mass transfer. In batch type electrolytic reactors, depletion of CO2 at the surface takes place first. CO2 from the bulk then has to diffuse to the electrode surface, resulting in mass transfer controlled kinetic phenomena. During the above process, several other competitive side reactions could suppress the primary reaction even though the cathode has good electro catalytic properties for reduction of carbon dioxide. When the dynamic supply of specific active species is ensured to electrode surface, the mass transfer effects are minimized to certain extent. Hence it is envisaged that a continuous flow reactor is more efficient for the electro-reduction of CO2 in CO2 saturated aqueous electrolytes. The primary reactions that occur at the copper electrode during the reduction of CO2 are listed below (with the standard potentials calculated using formation energies [1] :"

Jan 1, 2010

By Bin Xu, Qian Li, Yong-bin Yang, Xiao-liang Liu, Tao Jiang, Yan Zhang

Some high sulfur and arsenic-bearing gold concentrate has a gold leaching rate less than 80% by oxidation roasting-pickling-cyanidation process. The characteristics and intensification of gold leaching were studied systemically. By combining chemical composition and phase analysis, the low gold leaching rate was found to lie in the capsulation of gold by iron-containing phases including iron oxides, arsenopyrite and pyrite. 96.66% of gold in the industrial leaching residue was capsulated and 95.88% of the capsulated turned out to be in the iron-containing phases. The results of laboratory pickling-cyanidation experiments on the calcine and industrial leaching residue presented further demonstration for the fact that gold capsulated in the iron-containing phases was hard to be leached. However, the gold cyanide leaching rate of calcine could be raised over 95% by a reduction roasting-pickling pretreatment which played such a significant role in exposing the capsulated gold that gold leaching was intensified remarkably.

Jan 1, 2015

By Yuanbo Zhang, Yingming Chen, Zijian Su, Bingbing Liu, Jun Chen

Iron, tin-bearing tailings is a kind of hazardous solid waste generated from cassiterite dressing operation. It is difficult to utilize the tailings by present mineral processing methods due to the complex dissemination characteristics. In this study, a process of gas-based magnetizing roasting followed by magnetic separation was studied for separating and recovering iron from the tailings. The effects of roasting and magnetic separation parameters on the recovery of iron were systematically investigated. The optimum parameters were proposed as follows: CO/(CO+CO2) content of 5%, roasting temperature of 850 C, roasting time of 60 min, grinding particle size of 90% less than 45 μm and magnetic field intensity of 800 Gs. Under these conditions, the magnetic concentrate containing 68.5% Fe and 0.06% Sn was achieved, which can be used as high-quality raw materials for direct reduction iron production.

Jan 1, 2016

By Matsufumi Takaya, Yukihiro Sakamoto

"Electric field emission properties from CVD diamond fabricated using pulse-modulated microwave plasma CVD were studied. Diamond was synthesized by microwave plasma CVD apparatus equipped with a pulse-modulated microwave power supply. Pulse conditions were varied from 1 to 10 seconds for pulse periods and from 0.1 to lHz for pulse frequency either. Surface morphologies of the deposits were differed by pulse frequency and duty cycle. As a result, FE properties prepared by different pulse duty cycle were different from continuous film which synthesized using continuous microwave significantly. Highest current density was obtained from the uneven morphology diamond film prepared at 17.5% pulse duty cycle.FE properties of the CVD diamond were depended on surface morphologies that related to the pulse conditions.1. IntroductionDiamond has excellent physical and chemical properties as an industrial material. Especially, hydrogen terminated diamond had the negative electron affinity (NEA) 1) and CVD diamond has this NEA property either as deposited 2). So the electron emission source to the FED is expected as one of this application of CVD diamond as cold cathode of electric devices. We studied on FE properties of various CVD diamond, pulse microwave plasma CVD diamond showed better property than those of other CVD diamond 3).This report studied on· the effect of the duty-cycle of pulse modulate microwave condition on FE properties of the diamond fabricated by pulse modulated microwave plasma CVD."

Jan 1, 2000

By Robert W. Bartlett

Hazardous metal contaminants in liquid and solid wastes and from ground spills are important environmental problems in many metallurgical production operations. Acid rock drainage, from mines and huge quantities of permeable mine waste, is probably the most ubiquitous example. Fixing mine waste contaminants in situ has been practiced, using sulfate reducing bacteria (SRB) and organic reagents as electron donors to create anaerobic conditions and precipitate metal sulfides. Aqueous solutions of sugar and alcohol have been percolated into mine wastes with good results. However, maintaining anaerobic conditions permanently is unlikely, as these solutions are eventually washed out of solid waste and contaminated ground by inflow of either groundwater or meteoric water, allowing re-oxidation from entering air. Emulsions of inexpensive, non-aqueous organic microdroplets dispersed in water provide earth wettablility equal to aqueous solutions and easy percolation into both the ground and mine waste. Subsequent breakdown of the O/W emulsion provides permanent retention of the organic phase, attached to earth particles, that secures lasting anaerobic conditions, precipitates metals as sulfides and prevents re-oxidation of these sulfides. This process and its optimization are described, including experiments with sand-filled columns representing a vertical section through solid waste. Results of organic and metal retention in solid waste are provided from analyses of acid mine water drainage before and after waste treatment.

Jan 1, 2006

By Walter Curlook

An improved process of hydrometallurgical treatment of laterite ores of the limonitic type for the recovery of nickel and cobalt using sulphuric acid has been developed and patented [I]. The major improvement is brought about by recycling a significant portion of the "mother liquor" emanating from the pressure leaching reaction back to the feed preparation stage thereby substituting for all or at least a major proportion of the fresh water that must be added. The amount of process effluent waters is correspondingly reduced. Concomitantly with the major savings in fresh water requirements, a degree of reduction in new sulphuric acid requirements is effected, along with a savings in limestone and lime required for subsequent neutralizations. Keywords: Acid pressure leaching; Nickel laterites

Jan 1, 2004

By J. Rajek

The novel multi-component, multi-particle, multi-phase precipitation model developed recently is used to predict the precipitation kinetics in complex 9-12% Cr steels investigated within the European COST 522 project. These steels are used for tubes, pipes, casings and rotors in USC (ultra super critical) steam power plants for the 21st century. In the computer simulations, the evolution of the precipitate microstructure is monitored over the entire production heat treatment starting with the casting process, including austenizing, several annealing treatments and in-service conditions. The main interest lies on the concurrent growth and coarsening interaction of different types of precipitates. Keywords: Precipitation kinetics, heat treatment, power plant steels, simulation

Jan 1, 2003

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 Zemin Ma

A novel chromate [Cr(VI)] reducing bacterium was isolated from chromite ore processing residue disposal site of China and identified as a Leucobacter sp. by 16S rRNA gene sequence homology. The minimum inhibitory concentration of strain CRB1 was 820 mg l-1 of Cr(VI). The reduction of Cr(VI) occurred only under aerobic conditions. With an initial concentration of 2.5×108 cells ml-1, 1800 mg l-1 of Cr(VI) was reduced entirely within 38 h under the optimum conditions, at 30 °C and pH 9.0. Increasing Cr(VI) concentrations prolonged reduction process and higher cell densities meant quicker reduction. A blue precipitate was produced during chromate reduction of strain CRB1, which was binding to the surface of bacterial cells and determined as trivalent chromium with electron paramagnetic resonance (EPR) spectrometry. The conspicuous chromate reduction ability of Leucobacter sp. CRB1 suggested a potential for bioremediation of Cr(VI) containing wastes.

Jan 1, 2008

By J. L. Bill

The capacity of the Mount Isa Mimes Limited Copper Smelter was expanded in 1998 from 180,000 tomes per year of anode copper to 265,000 tpy. It is based on the innovative Copper ISASMELT technology, which currently treats concentrate at up to 184 tph. Increasing lance-air oxygen enrichment increased the ISASMELT furnace feed rate from 102 to 184 tph. The increased feed rate was achieved without any modifications to the ISASMELT furnace. The first refractory campaign following the upgrade lasted for two years. Future campaign lives of four years or more--without water cooling-are possible. Other Copper ISASMELT furnaces are operating in the U.S.A., Belgium, and India, with additional smelters under construction in China and Germany. In addition, Lead ISASMELT furnaces are operating in the U.K. and Malaysia. The paper discusses the performance of the MIM Copper ISASMELT furnace and the Copper Smelter since the expansion, including operating data and refractory performance.

Jan 1, 2002

By Xueming Lv

The rotary kiln-electric furnace (RKEF) process is the main method for producing ferronickel from nickel laterite ore. However, this process is energy intensive as it involves several high temperature steps. Therefore, a novel process is proposed to directly produce ferronickel from nickel laterite ore by semi-molten reduction, which is expected to be realized in a rotary hearth furnace (RHF). The RHF process is able to shorten the flow sheet, decrease the reaction temperature as well as reduce energy consumption. In this study, the influence of basicity on reduction of nickel laterite ore was investigated. The results showed that it is possible to produce the ferronickel nugget directly at 1400 °C when the quaternary basicity [(mCaO + mMgO)/(mSiO2 + mAl2O3)] was fixed at 0.60. Under this experimental condition, the grade and the recovery ratio of nickel reached 11.53% and 98.59%, and the grade and recovery ratio of Fe were 84.16% and 68.72%, respectively.

By Richard D. Hagni

Process mineralogy has not been given adequate attention in years past, because geologists have not been sufficiently interested in applying mineralogical techniques to industrial processes, and most process engineers are not adequately trained to use them. Although some individuals and institutions have made efforts to improve the situation, it is only in the last few years that the significance of applying the methods of mineralogy to a wide variety of industrial processes has been fully appreciated. Presently, the formation and organization of several groups devoted to applied mineralogy have created a more amenable climate for the development of process mineralogy. As a result, the presentation, discussion, and publication of the results and case histories of process mineralogy have become fairly common. Short courses affording hands-on experience with applied techniques are now available to the many geologists and process engineers engaged in industrial mineralogical processes. The future role of the process mineralogist is viewed as an expanded one, which will increase in value.

Jan 1, 1982

By Chang Wei, Zhigan Deng, Minting Li, Cunxiong Li, Xingbin Li

A direct hydrometallurgical process of extraction molybdenum and nickel from molybdenum-nickel ore by pressure water leaching without reagent was studied. The extraction of Mo and Ni from molybdenum-nickel ore by oxygen pressure leaching, which exploit the characteristic of molybdenum-nickel minerals contain high concentration amorphous sulfide which has highly active, and make the most of easily oxide to sulfuric acid and sulfate at low temperature and excess oxygen presence of the amorphous sulfide. Under oxygen pressure conditions, considerable molybdenum and almost all the nickel were extracted into solution in the leaching process. The results show that with the leaching time for 3~4h, temperature at 150o C, liquid-to-solid ratio of 2mL/g, mineral granularity of 0.074mm, oxygen partial pressure of 0.4~0.5MPa without other reagent, molybdenum leaching percentage can be over 80% and nickel leaching percentage can be more than 97%. Furthermore, about 80% sulfur in the Mo-Ni ore has been transformed into sulfuric acid.

Jan 1, 2014

By Onuralp Yucel, Ahmet Turan, K. Can Candeger

Exothermic riser sleeves are important tools to increase solidification duration, particularly for iron-steel casting. Increasing the time to solidus improved casting product quality by minimizing cavities. Therefore, process costs were significantly reduced. In comparison with the use of unsleeved risers, exothermic riser sleeves retain up to 30–35% of the heat and increase the duration to solidus by nearly 50%. Exothermic riser sleeves are a mixture of metallothermic-based exothermic and insulating materials that are manufactured in different sizes and shapes. Various suppliers produce these sleeves in different compositions. However, the designers must clearly understand the thermochemical and thermophysical properties. The purpose of the present study was to experimentally determine the effects of varying experimental parameters such as reaction duration, flammability and temperature change etc. on selected exothermic sleeves. The results were compared with thermodynamical simulations which were performed using the contents and the corresponding thermophysical properties of exothermic sleeves.

Mar 1, 2018

By Muhlis Nezihi Saridede, Burak Birol

"Plastic wastes become a huge problem day after day due to the growth of plastic industry. Hence, plastic wastes are used as a raw material for other industries to eliminate this problem. Polyethylene Terephthalate (PET), which is a commonly used for plastic bottles, may be used as a reductant for iron production because of its C and H content. In this study, composite pellets containing iron ore concentrate, flux and reductant were prepared. Crystallized PET bottles and coke were used as reductant after ground. The prepared pellets were reduced at 1400°C for 30 min. and iron nuggets were produced successfully. Usage of waste PET purely as reductant in composite pellets gives a higher metallization degree and proper carbon content than coke or PET and coke mixture.IntroductionPlastics can be seen everywhere, especially at packaging industry in our common life. The increase of plastic usage ends up with an important problem, the increase of plastic wastes. Many studies have been carried out about usage of plastics as reductant in blast furnace such as Ogaki et al.[1], Heo and Baek [2], Saridede [3], Minoru et al.[4], etc. Besides, Kato et al. [5], Nomura and Kato [ 6] and Rongfang et al. [7] have pointed out the use of plastics in coke ovens regarding to its calorific content. In EAF steelmaking, a mixture of coal/coke and plastics can be used as an energy resource instead of only coal or coke. [8] Also, the usage of PET and PC in self-reducing composite pellets increased the reduction rate. [12]PET (Polyethylene terephthalate ), which is commonly used for soft drink plastic bottles, is an important municipal waste due to its C and H content. Its molecular formula is (C10H8O 4)n. Demir and Dincer showed that PET can be crystallized at 250°C to have the ability to be ground to a size of -100 µm. [11]"

Jan 1, 2011