| 1. |
- Abbasalizadeh, Aida, et al.
(författare)
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Electrochemical Extraction of Rare Earth Metals in Molten Fluorides : Conversion of Rare Earth Oxides into Rare Earth Fluorides Using Fluoride Additives
- 2017
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Ingår i: JOURNAL OF SUSTAINABLE METALLURGY. - : SPRINGER. - 2199-3823 .- 2199-3831. ; 3:3, s. 627-637
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Tidskriftsartikel (refereegranskat)abstract
- In the present research on rare earth extraction from rare earth oxides (REOs), conversion of rare earth oxides into rare earth fluorides with fluoride fluxes is investigated in order to overcome the problem of low solubility of the rare earth oxides in molten fluoride salts as well as the formation of oxyfluorides in the fluorination process. Based on thermodynamic calculations, a series of experiments were performed for converting the rare earth oxides into rare earth fluorides using AlF3, ZnF2, FeF3, and Na3AlF6 as fluorinating agents in a LiF-Nd2O3 system. The formation of neodymium fluoride as a result of the reactions between these fluxes and neodymium oxide is confirmed. The rare earth fluoride thus formed can subsequently be processed through the electrolysis route in the same reactor, and rare earth metal can be produced as the cathodic deposit. In this concept, the REO dissolution in molten fluorides would become unnecessary due to the complete conversion of the oxide into the fluoride, REF3. The results of XRD and EPMA analysis of the reacted samples indicate that AlF3, ZnF2, and FeF3 can act as strong fluorinating agents for the neodymium oxide giving rise to a complete conversion of neodymium oxide into neodymium fluoride.
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| 2. |
- Abbasalizadeh, Aida, et al.
(författare)
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Electrochemical Recovery of Rare Earth Elements from Magnets : Conversion of Rare Earth Based Metals into Rare Earth Fluorides in Molten Salts
- 2017
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Ingår i: Materials transactions. - : JAPAN INST METALS. - 1345-9678 .- 1347-5320. ; 58:3, s. 400-405
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Tidskriftsartikel (refereegranskat)abstract
- In the present work, selective extraction of rare earth (RE) metals from NdFeB magnets is investigated by studying the effects of various fluxes, viz. AlF3, ZnF2, FeF3 and Na3AlF6 in the LiF-NdFeB system. The aim is to convert RE from RE magnet into the fluoride salt melt. The results show the complete selective separation of neodymium (also dysprosium) from the magnet and formation of rare earth fluoride, leaving iron and boron unreacted. The formed rare earth fluoride can subsequently be processed in the same reactor through an electrolysis route so that RE can be deposited as a cathode product. The results of XRD and EPMA analysis of the reacted samples indicate that AlF3, ZnF2 and FeF3 can act as strong fluorinating agents for extraction of rare earth from NdFeB magnet, converting the RE to REF3. The results confirm the feasibility of the rare earth metals recovery from scrap NdFeB magnet as raw material. The fluoride conversion- electrolysis route suggested in the present work enables the extraction of rare earth metals in a single step using the above-mentioned fluxes.
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| 3. |
- Abbasalizadeh, A., et al.
(författare)
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Experimental investigation and thermodynamic modelling of LiF-NdF3-DyF3 system
- 2018
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Ingår i: Journal of Alloys and Compounds. - : Elsevier. - 0925-8388 .- 1873-4669. ; 753, s. 388-394
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Tidskriftsartikel (refereegranskat)abstract
- Electrolysis of molten fluorides is one of the promising methods for the recovery and recycling of rare earth metals from used magnets. Due to the dearth of phase equilibria data for molten fluoride systems, thermodynamic modelling of LiF-DyF3-NdF3 system using the CALPHAD approach was carried out. Gibbs energy modelling for LiF-NdF3 and LiF-DyF3 systems was performed using the constitutional data from literature. Ab initio calculations were used to obtain enthalpy of reaction of LiDyF4, an intermediate phase that is found to exist in the LiF-DyF3 system. Differential thermal analysis was carried out for selected compositions in the NdF3-DyF3 system, in order to determine liquidus and solidus temperatures. The Gibbs energy parameters for the limiting binaries determined in this work is used for modelling the Gibbs energy functions of equilibrium phases in the ternary system. Selected compositions of LiF-NdF3-DyF3 were subjected to DTA in order to validate the calculated phase temperatures involving melt.
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| 4. |
- Abbasalizadeh, Aida, et al.
(författare)
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Highlights of the Salt Extraction Process
- 2013
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Ingår i: JOM. - : Springer Science and Business Media LLC. - 1047-4838 .- 1543-1851. ; 65:11, s. 1552-1558
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Tidskriftsartikel (refereegranskat)abstract
- This article presents the salient features of a new process for the recovery of metal values from secondary sources and waste materials such as slag and flue dusts. It is also feasible in extracting metals such as nickel and cobalt from ores that normally are difficult to enrich and process metallurgically. The salt extraction process is based on extraction of the metals from the raw materials by a molten salt bath consisting of NaCl, LiCl, and KCl corresponding to the eutectic composition with AlCl3 as the chlorinating agent. The process is operated in the temperature range 973 K (700 degrees C) to 1173 K (900 degrees C). The process was shown to be successful in extracting Cr and Fe from electric arc furnace (EAF) slag. Electrolytic copper could be produced from copper concentrate based on chalcopyrite in a single step. Conducting the process in oxygen-free atmosphere, sulfur could be captured in the elemental form. The method proved to be successful in extracting lead from spent cathode ray tubes. In order to prevent the loss of AlCl3 in the vapor form and also chlorine gas emission at the cathode during the electrolysis, liquid aluminum was used. The process was shown to be successful in extracting Nd and Dy from magnetic scrap. The method is a highly promising process route for the recovery of strategic metals. It also has the added advantage of being environmentally friendly.
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| 5. |
- Abbasalizadeh, Aida, et al.
(författare)
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Neodymium extraction using salt extraction process
- 2015
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Ingår i: Mineral Processing and Extractive Metallurgy. - : Maney Publishing. - 0371-9553 .- 1743-2855. ; 124:4, s. 191-198
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Tidskriftsartikel (refereegranskat)abstract
- The present paper deals with the feasibility of the neodymium recovery from spent Nd-Fe-B magnets using molten salt electrodeposition method. The salt bath consisted of a mixture of LiCl- KCl-NaCl corresponding to the eutectic composition. The experimental set-up with its salient features is presented. AlCl3 was used as flux and graphite rods dipped in the salt bath served as electrodes. The voltage for the electrolysis was chosen on the basis of the decomposition potential of NdCl3. The reaction sequence can be described as Iron-free neodymium deposition could be carried out successfully. In view of the proximity of the electrode potentials, the co-deposition of the aluminium and neodymium was observed to occur at the cathode, as revealed by SEM/EDS and XRD analyses of the electrodeposit.
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| 6. |
- Abbasalizadeh, Aida, et al.
(författare)
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Novel Reactive Anode for Electrochemical Extraction of Rare Earth Metals from Rare Earth Oxides
- 2017
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Ingår i: RARE METAL TECHNOLOGY 2017. - Cham : SPRINGER INTERNATIONAL PUBLISHING AG. ; , s. 87-92
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Konferensbidrag (refereegranskat)abstract
- Electrolytic production of metallic neodymium is carried out in fused fluoride salts containing neodymium oxide. Two major challenges pertaining to neodymium production are (a) low oxide solubility, (b) possibility of anodic fluorine gas evolution if the electrolysis rate exceeds feeding rate of neodymium oxide. In this study, a novel method is proposed in which iron fluoride (FeF3) is used as a fluorinating agent to convert neodymium oxide into neodymium fluoride. Electron Probe Micro Analysis (EPMA) results of as-converted salt show a complete conversion of neodymium oxide into neodymium fluoride. In the electrolysis process, iron is used as a reactive anode with electrochemical dissolution of iron into the melt, thus preventing fluorine gas evolution at the anode. Therefore, the fluorinating agent is constantly regenerated in situ which enables the continuous conversion of neodymium oxide feed. The cathodic product is a Nd-Fe alloy which can be directly used as a master alloy for the production of NdFeB permanent magnets.
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| 7. |
- Abbasalizadeh, A., et al.
(författare)
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Rare Earth Extraction from NdFeB Magnets and Rare Earth Oxides Using Aluminum Chloride/Fluoride Molten Salts
- 2015
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Ingår i: Rare Earths Industry. - : Elsevier. - 9780128023280 ; , s. 357-373
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Bokkapitel (övrigt vetenskapligt/konstnärligt)abstract
- In the current research, the feasibility of the recovery of neodymium and dysprosium from spent NdFeB magnets (about 6wt% Dy) was investigated using molten salt processes. The salt bath consisted of a eutectic composition of an NaCl-KCl-LiCl mixture. To enable the efficient dissolution of metal in the molten salt phase, AlCl3 was used as a chlorinating agent. Iron-free electrodeposition was carried out successfully. Energy-dispersive spectroscopic analysis of the electrodeposit revealed that co-deposition of the dysprosium occurs along with neodymium at the cathode. The process shows that this method is well suited for recovering rare earth metals from magnetic scrap containing these metals.Furthermore, the setup design for recovery of neodymium and dysprosium from their oxides was investigated with regard to previous studies on the neodymium magnets. The stability of different fluoride and chloride salts was studied by means of thermodynamic calculation. Aluminum fluoride-based molten salt systems were studied in detail as the electrolyte for electrochemical extraction of rare earth oxides into rare earth metal elements with Al.
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| 8. |
- Abbasalizadeh, Aida, et al.
(författare)
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Use of iron reactive anode in electrowinning of neodymium from neodymium oxide
- 2019
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Ingår i: Electrochimica Acta. - : PERGAMON-ELSEVIER SCIENCE LTD. - 0013-4686 .- 1873-3859. ; 310, s. 146-152
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Tidskriftsartikel (refereegranskat)abstract
- Electrolytic production of metallic neodymium is carried out in fused neodymium fluoride salts containing neodymium oxide. Two major challenges pertaining to neodymium production in fluoride salts are a) low solubility of neodymium oxide in fluoride melt, b) possibility of anodic gas evolution (CO, CO2, CF4, C2F6). In this study, iron is used as a reactive anode in the electrolysis process, promoting electrochemical dissolution of iron into the melt, preventing PFC (perfluorocarbon) gas evolution at the anode. Further, the rare earth oxide is converted to rare earth fluoride by the use of iron fluoride formed as the result of iron dissolution. Thus, the fluoridizing agent is constantly regenerated in-situ which enables the continuous conversion of neodymium oxide feed. The cathodic product is Nd-Fe alloy which can be used as a master alloy for the production of NdFeB magnets.
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| 9. |
- Abdul Abas, Riad
(författare)
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Experimental Studies of Thermal Diffusivities concerning some Industrially Important Systems
- 2006
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- The main objective of this industrially important work was to gain an increasing understanding of the properties of some industrially important materials such as CMSX-4 nickel base super alloy, 90Ti.6Al.4V alloy, 25Cr:6Ni stainless steel, 0.7% carbon steel, AISI 304 stainless steel-alumina composites, mould powder used in continuous casting of steel as well as coke used in blast furnace with special reference to the thermal diffusivities. The measurements were carried out in a wide temperature range covering solid, liquid, glassy and crystalline states. For CMSX-4 alloy, the thermal conductivities were calculated from the experimental thermal diffusivities. Both the diffusivities and conductivities were found to increase with increasing temperature. Microscopic analysis showed the presence of intermetallic phases γ´ such as Ni3Al below 1253 K. In this region, the mean free path of the electrons and phonons is likely to be limited by scattering against lattice defects. Between 1253 K and solidus temperature, these phases dissolved in the alloy adding to the impurities in the matrix, which, in turn, caused a decrease in the thermal diffusivity. This effect was confirmed by annealing the samples at 1573 K. The thermal diffusivities of the annealed samples measured at 1277, 1403 and 1531 K were found to be lower than the thermal diffusivities of non-annealed samples and the values did not show any noticeable change with time. It could be related to the attainment of equilibrium with the completion of the dissolution of γ´ phase during the annealing process. Liquid CMSX-4 does not show any change of thermal diffusivity with temperature. It may be attributed to the decrease of the mean free path being shorter than characteristic distance between two neighbouring atoms. Same tendency could be observed in the case of 90Ti.6Al.4V alloy. Since the thermal diffusivity increases with increasing temperature below 1225 K and shows slight decrease or constancy at higher temperature. For 25Cr:6Ni stainless steel, the thermal diffusivity is nearly constant up to about 700 K. Beyond that, there is an increase with temperature both during heating as well as cooling cycle. On the other hand, the slope of the curve increases above 950 K, which can be due to the increase of bcc phase in the structure. 0.7% carbon steel shows a decrease in the thermal diffusivity at temperature below Curie point, where the structure contains bcc+ fcc phases. Above this point the thermal diffusivity increases, where the structure contains only fcc phase. The experimental thermal conductivity values of these alloys show good agreement with the calculated values using Mills model. Thermal diffusivity measurements as a function of temperature of sintered AISI 304 stainless steel-alumina composites having various composition, viz, 0.001, 0.01, 0.1, 1, 2, 3, 5, 7, 8 and 10 wt% Al2O3 were carried out in the present work. The thermal diffusivity as well as the thermal conductivity were found to increase with temperature for all composite specimens. The thermal diffusivity/conductivity decreases with increasing weight fraction of alumina in the composites. The experimental results are in good agreement with simple rule of mixture, Eucken equation and developed Ohm´s law model at weight fraction of alumina below 5 wt%. Beyond this, the thermal diffusivity/ conductivity exhibits a high discrepancy probably due to the agglomeration of alumina particles during cold pressing and sintering. On the other hand, thermal diffusivities of industrial mould flux having glassy and crystalline states decrease with increasing temperature at lower temperature and are constant at higher temperature except for one glassy sample. The thermal diffusivity is increased with increasing crystallisation degree of mould flux, which is expected from theoretical considerations. Analogously, the thermal diffusivity measurements of mould flux do not show any significant change with temperature in liquid state. It is likely to be due to the silicate network being largely broken down. In the case of coke, the sample taken from deeper level of the pilot blast furnace is found to have larger thermal diffusivity. This can be correlated to the average crystallite size along the structural c-axis, Lc, which is indicative of the higher degree of graphitisation. This was also confirmed by XRD measurements of the different coke samples. The degree of graphitisation was found to increase with increasing temperature. Further, XRD and heat capacity measurements of coke samples taken from different levels in the shaft of the pilot blast furnace show that the graphitisation of coke was instantaneous between 973 and 1473 K.
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| 10. |
- Abdul Abas, Riad, et al.
(författare)
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Studies on Graphitisation of Blast Furnace Coke by X-ray Diffraction Analysis and Thermal Diffusivity Measurements
- 2005
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Ingår i: Steel research. - : Wiley. - 0177-4832 .- 1611-3683. ; 77:11, s. 763-769
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Tidskriftsartikel (refereegranskat)abstract
- High temperature XRD and thermal diffusivity experiments were employed to investigate the degree of graphitisation in blast furnace coke. The experiments were conducted between room temperature and 1473 K. X-ray diffraction studies were carried out in order to monitor the degree of graphitisation in the coke samples from the same campaign. In these cases, the degree of graphitisation was followed by the changes in the vertical dimension. The degree of graphitisation was found to be dependent on temperature. On the other hand, the graphitisation at each temperature was instantaneous, even at as low a temperature as 973 K and no dependency on time could be noticed. The thermal diffusivities of the coke samples taken from deeper level of the experimental blast furnace were measured using the laser-flash technique. The results from these measurements showed that thermal diffusivities increased with the degree of graphitisation, which in turn, can be affected by the level in the blast furnace at which the coke sample was taken. The present results indicate that the degree of graphitisation as followed by X-ray diffraction analysis as well as thermal diffusivities can be used to trace the thermal history of coke. DSC measurements show that the heat capacity of the coke increases with temperature towards the heat capacity of graphite, which could be due to the increasing the graphitisation degree of the coke.
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