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Article

Synthesis of Mg–Zn–Nd Master Alloy in Metallothermic Reduction of Neodymium from Fluoride–Chloride Melt

1
The Automation of Technological Processes and Production Department, Saint Petersburg Mining University, 199106 Saint Petersburg, Russia
2
Patent and Licensing Department, Saint-Petersburg Mining University, 199106 Saint Petersburg, Russia
3
The Automation of Technological Processes and Production Department, Saint-Petersburg Mining University, 199106 Saint Petersburg, Russia
4
Research of Technische Universität Bergakademie Freiberg, 09599 Freiberg, Germany
*
Author to whom correspondence should be addressed.
Crystals 2020, 10(11), 985; https://doi.org/10.3390/cryst10110985
Submission received: 26 September 2020 / Revised: 27 October 2020 / Accepted: 29 October 2020 / Published: 30 October 2020
(This article belongs to the Special Issue Intermetallic Compound)

Abstract

:
In the presented article, a differential thermal analysis was carried out and the temperatures of thermal effects were established that arise during the reduction of neodymium from a technological salt mixture KCl–NaCl–CaCl2–NdF3 with a magnesium–zinc alloy. The results of experimental studies on the reduction of neodymium from a fluoride–chloride melt in a shaft electric furnace at temperatures of 550, 600, 650, 700 °C are presented. In order to increase the degree of extraction of neodymium into the Mg–Zn–Nd master alloy, the study of the influence of technological parameters on the degree of extraction of neodymium was carried out. It was experimentally proven that when zinc is added to a reducing agent (magnesium), the degree of extraction of neodymium into the master alloy is 99.5–99.7%. The structure of the obtained master alloy samples, characterized by a uniform distribution of ternary intermetallic compounds (Mg3,4NdZn7) in the volume of a double magnesium–zinc eutectic, was studied by optical and electron microscopy.

Graphical Abstract

1. Introduction

The addition of neodymium into the magnesium–zinc–zirconium system leads to a change in the phase composition of magnesium-based alloys. In this case, simultaneously with the known strengthening phases of magnesium with neodymium (for example, Mg12Nd), phases of a more complex stoichiometric composition are formed, containing magnesium, neodymium, and zinc, for example Nd15Mg65Zn20, Nd16Mg37Zn47, Nd6Mg41Zn53 [1,2,3,4,5,6,7]. Due to the presence of these phases in the system, a combination of highly plastic and structural characteristics of magnesium alloys, as well as their high-temperature strength, is ensured, since the thermal expansion coefficient of long period stacking ordered (LPSO) phases is much lower than that of the basic α-solid solution [8,9,10,11].
It is known that the production of magnesium and aluminum alloys is carried out by dissolving in the melt double and ternary master alloys, which are produced by fusing the components, using metallothermic reduction of alloying components from their compounds (for example, oxides or fluorides) or electrolysis [12,13,14,15]. In recent years, there has been a tendency to produce more complex master alloys, for example, ternary or quadruple [16,17,18]. It was found that ternary master alloys can be effectively used in the production of alloys based on light metals [19,20].
In this regard, it seems relevant to develop new solutions for the production of complex magnesium master alloys including rare earth metals (REEs). It should be noted that for the domestic magnesium industry the task of obtaining magnesium alloys is of great importance in connection with the approval of the Strategy for the development of the metallurgical industry in Russia for the period up to 2030. In accordance with the sustainable development plan, the task of increasing the production of metallurgical products with high added value was approved, which should lead to a reduction in imports of such products [21]. In addition, the state′s priority is to improve the quality of production of Russian metallurgical companies in order to increase the efficiency of processing mineral raw materials [22,23,24,25,26,27,28,29].
The aim of the work is to develop technological solutions that ensure high extraction of neodymium in the ternary Mg–Zn–Nd master alloy during metallothermic reduction of neodymium fluoride, which can be used in the production of high-strength and heat-resistant magnesium and aluminum alloys.

2. Materials and Methods

Differential thermal analysis (DTA) was carried out using a (NETZSCH, Selb, Germany) Simultaneous thermal analyzer (STA 429 CD) in a high purity argon flow at a gas flow rate of 50 mL per minute [30]. For the analysis, a salt mixture 35KCl–35NaCl–30CaCl2–NdF3, granular zinc and magnesium were weighed into an alundum melting pot. Two heating–cooling cycles were carried out at a rate of 10 °C per minute. In the first cycle, the melting pot with the weighed portion was heated to a temperature of 800 °C, then cooled to 200 °C; in the second successive cycle, the melting pot was heated from 200 to 800 °C and cooled again.
Experimental studies were carried out on a laboratory setup, which includes the following items: the shaft electric furnace with silicon carbide heating elements, the thermostat, the furnace control panel, the thermocouple and the stirring device. The synthesis of ternary master alloy Mg–Zn–Nd was carried out according to the following procedure. A mixture of salts consisting of Potassium chloride, (35 wt.%), Sodium chloride (35 wt.%), Calcium chloride (30 wt.%) was previously prepared. To this mixture was added neodymium fluoride (NdF3) and the mixture stirred continuously. Then the resulting technological salt mixture was added to magnesium and zinc and placed in an alundum melting pot in the furnace. In the first series of experiments, in order to determine the optimal temperature condition for the synthesis of the master alloy, the melting pot was kept in a furnace with temperatures variations from 550 to 700 °C, and the residence time from 15 to 30 min, with a constant ratio of chlorides to neodymium fluoride. In the second series of experiments, in order to identify the most optimal technological condition, the synthesis temperature was varied from 650 to 700 °C, the residence time from 20 to 30 min, the ratio of chlorides to neodymium fluoride from 1:4 to 1:6. After the exposure time, in all experiments, the melt was settled for 5 min. The surface part of the molten salt was poured out, and the resulting master alloy was poured into molds. The studies were carried out with a constant mass ratio of Mg: Zn 1:2 and components of the salt mixture 35KCl–35NaCl–30CaCl2, the qualifications of the initial salts of the mixture are: KCl, NaCl, CaCl2,—chemically pure, NdF3—pure. The average values of the degree extraction for neodymium obtained from the results of three parallel experiments are presented in the discussion of the results.
Elemental analysis of master alloy samples, which were obtained after DTA and experiments on a laboratory setup, was carried out on the sequential Wavelength Dispersive X-Ray Fluorescence Spectrometer XRF-1800 (Shimadzu, Kyoto, Japan). The metallographic study for the samples of the obtained master alloy was carried out on the Axiovert 40 MAT optical microscope (Carl Zeiss, Oberkochen, Germany) and the VEGA electron microscope (TESCAN, Brno, Czech Republic) with the INCAx-act energy dispersive spectrometer (Oxford Instruments, Abingdon, UK). The research was carried out with the involvement of the laboratory facilities of the Common Use Center of the Saint-Petersburg Mining University.

3. Results

At the first stage of experimental studies, DTA of the reduction process for neodymium from a technological salt mixture with a magnesium–zinc alloy was carried out. Figure 1 shows the thermograms obtained in the first heating cycle (green line of the curve) and the second heating cycle (purple line of the curve) of the Mg–Zn–KCl–NaCl–CaCl2–NdF3 sample up to 800 °C.
During the first cycle of heating the charge, the beginning of zinc melting was recorded at a temperature of 413 °C. It was accompanied by an endothermic effect with a maximum at 431 °C. The interaction with magnesium begins after the zinc melts, which is confirmed by a strong exothermic effect with a minimum at 476 °C. It is typical for the process of formation of intermetallic compounds from pure elements. The exothermic peak with a minimum at 486 °C cannot be interpreted since it is associated with the uneven melting of the charge and the peculiarity of filling the melting pot. The onset of the reduction of neodymium by magnesium–zinc melt from fluoride in the chloride melt was recorded at a temperature of 522 °C after the end of the interaction of magnesium and zinc. This is confirmed by an extended exothermic effect with a minimum at 566 °C. The endothermic effect with a maximum at 703 °C corresponds to the melting of the components of the technological salt mixture, and at the temperature of 731 °C all interactions in the system under study cease. During the second heating cycle, the thermogram recorded endothermic effects of melting of the magnesium-zinc alloy with a maximum at 347 °C and a ternary master alloy with a maximum at 532 °C It was found that this effect corresponds to the melting of a ternary compound MgxNdyZnz [7].
Figure 2 shows the thermograms obtained in the first cooling cycle (blue line) and the second cooling cycle (brown line) of the Mg–Zn–KCl–NaCl–CaCl2–NdF3 sample up to 200 °C.
During the first and second cooling cycles, two thermal effects were revealed on the thermograms. The first with the minimum at 326 °C, corresponding to the crystallization of the double magnesium–zinc eutectic. The second at 511–512 °C, corresponding to the crystallization of the MgxNdyZnz ternary compound. In addition, thermal effects were recorded at the temperature of 494 °C, corresponding to the crystallization of the reacted technological salt mixture. Elemental analysis of the obtained sample for the magnesium–zinc–neodymium master alloy showed the presence of 18.11 wt.% neodymium, which proves the fundamental possibility of obtaining the master alloy at temperatures up to 700 °C and indicates the process of the reduction of neodymium from the fluoride–chloride melt with the magnesium–zinc alloy (Table 1).
In the first series of experiments, the temperature effect on the degree of neodymium extraction was studied during experimental research on the neodymium reduction from a fluoride–chloride melt in a shaft electric furnace. In this case, in order to reduce the temperature for the synthesis of the ternary master alloy was taken the constant value of the Mg:Zn ratio equal to 1:2 [31]. As a result of processing the obtained data, the dependences of the degree of extraction of neodymium on the residence time at temperatures of 550, 600, 650, 700 °C were assessed (Figure 3).
During the experiments, it was confirmed that the addition of zinc to the charge helps to reduce the temperature of the neodymium reduction process from the molten salt, in contrast to the temperature ranges for obtaining the double magnesium–neodymium master alloy [32]. It was found that the degree of extraction of neodymium of up to 60% is achieved at a synthesis temperature of 550 °C. Moreover, the degree of extraction of neodymium increases to 92.2–93.2% with an increase in temperature to 650 °C
In the second series of experiments, studies were carried out in order to identify the most optimal technological parameters for conducting melts. In this case, a high degree of neodymium extraction into the maser alloy is achieved. The initial data and the results of experiments on obtaining the master alloy are shown in Table 2.
It was determined that the neodymium fluoride reduction is accompanied by the formation of the homogeneous magnesium–zinc–neodymium master alloy. According to experimental data, it has been proved that the neodymium yield increases to 99.6% with an increase in the ratio of chlorides to NdF3 up to 6:1 in the technological salt mixture and with continuous stirring of the melt. With an increase in temperature up to 700 °C, the neodymium yield does not change significantly. As a result of the performed melts, master alloys with a neodymium content of 10 to 25 wt.% were obtained. Analysis of the quality of the resulting master alloy showed that its macrostructure is characterized by the absence of gas pores and non-metallic inclusions (Figure 4).
Since there are no regulatory requirements for the ternary master alloy of the studied composition, the comparison was made with the requirements for the content of impurities for the magnesium–neodymium alloy; this one is also used for the production of special-purpose magnesium alloys. The Mg–Zn–Nd master alloys meets the requirements for Mg–Nd magnesium master alloys according to specification TU 48-4-271-91 (Table 3).
The microstructure of all tested master alloys in the cast state consisted of a magnesium–zinc matrix, and well-distinguishable individual intermetallic compounds, mainly polygon-shaped. Regular shapes and some coagulation of the edges can be detected, which ultimately leads to the absence of local defects in the microstructure in the matrix. A significant part of the thin section for the obtained magnesium–zinc–neodymium master alloy with a content of 24.8 wt.% neodymium (Figure 5a) is occupied by eutectic colonies (dark areas). It is located along the boundaries of the individual intermetallic compounds (light areas). In some cases, areas of accretion of intermetallic compounds are observed. The average grain diameter is 35 µm. Zones of eutectics are revealed at ×500 magnification (Figure 5b). They are located within the individual intermetallic compounds.
Micro X-ray spectral analysis of the structure sections shows (Figure 6a) that individual intermetallic compounds contain about 21 wt.% neodymium, which corresponds to the Mg3,4NdZn7 phase. Double eutectic (Figure 6b), alloyed with neodymium, contains 32.41 wt.% magnesium, 60.72 wt.% zinc and 6.88 wt.% neodymium (Table 4).

4. Conclusions

Thus, as a result of the experimental studies, a ternary master alloy of magnesium–zinc–neodymium was obtained, while optimal technological conditions of the synthesis were revealed (temperature 650 °C, residence time 20 min, ratio of chlorides to neodymium fluoride 1:6, while stirring the melt), in this case, the degree of extraction of neodymium achieved is up to 99.6%.
It was established that the onset of the reduction of neodymium by magnesium–zinc melt from its fluoride in the chloride melt occurs at a temperature of 522 °C using DTA. This is confirmed by an extended exothermic effect with a minimum at 566 °C.
Analysis of the microstructure showed that the obtained ternary master alloy 25Mg–50Zn–25Nd is characterized by a uniform distribution of intermetallic compounds (Mg3NdZn6) in the bulk of the double magnesium–zinc eutectic. The obtained experimental data are a prerequisite for the development of industrial technology for the production of magnesium–zinc–neodymium alloys for their use in non-ferrous and ferrous metallurgy.

Author Contributions

Conceptualization, I.B.; methodology, S.S.; software, I.B.; validation, S.S., I.B., R.K.; formal analysis, V.B.; investigation, I B.; resources, S.S.; writing—original draft preparation, S.S.; writing—review and editing, R.K. and V.B.; visualization, I.B.; supervision, R.K.; project administration, I.B.; funding acquisition, I.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The authors thank St. Petersburg Mining University for the opportunity to realize research. The studies were performed using the equipment of the Common Use Centre of the Saint-Petersburg Mining University.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Thermograms of the first (green) and second (purple) heating cycle of the sample Mg–Zn–KCl–NaCl–CaCl2–NdF3 up to 800 °C.
Figure 1. Thermograms of the first (green) and second (purple) heating cycle of the sample Mg–Zn–KCl–NaCl–CaCl2–NdF3 up to 800 °C.
Crystals 10 00985 g001
Figure 2. Thermograms of the first (blue) and second (brown) cooling cycle of the sample Mg–Zn–KCl–NaCl–CaCl2–NdF3 up to 200 °C.
Figure 2. Thermograms of the first (blue) and second (brown) cooling cycle of the sample Mg–Zn–KCl–NaCl–CaCl2–NdF3 up to 200 °C.
Crystals 10 00985 g002
Figure 3. Dependence of the degree of extraction of neodymium and the residence time at temperatures of 550–700 °C.
Figure 3. Dependence of the degree of extraction of neodymium and the residence time at temperatures of 550–700 °C.
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Figure 4. Macrostructure of master alloy 25Mg–50Zn–25Nd.
Figure 4. Macrostructure of master alloy 25Mg–50Zn–25Nd.
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Figure 5. Microstructure of master alloy 25Mg–50Zn–25Nd. Zoom (a) ×100, and (b) ×500.
Figure 5. Microstructure of master alloy 25Mg–50Zn–25Nd. Zoom (a) ×100, and (b) ×500.
Crystals 10 00985 g005
Figure 6. Electronic images of the microstructure of the 25Mg–50Zn–25Nd master alloy (a) and (b)—×2000.
Figure 6. Electronic images of the microstructure of the 25Mg–50Zn–25Nd master alloy (a) and (b)—×2000.
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Table 1. Chemical composition of Mg–Zn–Nd master alloy.
Table 1. Chemical composition of Mg–Zn–Nd master alloy.
Master Alloy Mass Fraction, %
Main ComponentsImpurities
ZnMgNdFeCuNiSiAl
Mg–Zn–Nd, 53.4628.1518.110.120.060.010.050.04
Table 2. Results of synthesis of Mg–Zn–Nd master alloy.
Table 2. Results of synthesis of Mg–Zn–Nd master alloy.
Melt NumberChloride Ratio: NdF3T, °Ct, minStirringNd Recovery, %
14:165020no86.9
26:165020no95.8
34:170020yes88.1
46:170020yes99.6
54:165030yes88.4
66:165030yes99.5
74:170030no88.1
86:170030no96.3
94:165020yes86.2
106:165020yes99.6
114:170020no85.2
126:170020no91.4
134:165030no84.3
146:165030no93.6
154:170030yes87.9
166:170030yes99.6
Table 3. Chemical composition of Mg–Zn–Nd master alloy.
Table 3. Chemical composition of Mg–Zn–Nd master alloy.
Alloy GradeMass Traction, %
Main ComponentsImpurities, max
ZnMgREEsFeCuNiSiAl
MH-base20–350.150.10.010.050.05
Mg–Zn–Nd, melting №16base25.024.80.080.06-0.030.02
Table 4. Values of spectra of Mg–Zn–Nd master alloy.
Table 4. Values of spectra of Mg–Zn–Nd master alloy.
SpectrumMg, wt.%.Zn, wt.%.Nd, wt.%.
spectrum 1 (a)12.0866.7321.19
spectrum 2 (b)32.4160.726.88
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Beloglazov, I.; Savchenkov, S.; Bazhin, V.; Kawalla, R. Synthesis of Mg–Zn–Nd Master Alloy in Metallothermic Reduction of Neodymium from Fluoride–Chloride Melt. Crystals 2020, 10, 985. https://doi.org/10.3390/cryst10110985

AMA Style

Beloglazov I, Savchenkov S, Bazhin V, Kawalla R. Synthesis of Mg–Zn–Nd Master Alloy in Metallothermic Reduction of Neodymium from Fluoride–Chloride Melt. Crystals. 2020; 10(11):985. https://doi.org/10.3390/cryst10110985

Chicago/Turabian Style

Beloglazov, Ilia, Sergey Savchenkov, Vladimir Bazhin, and Rudolf Kawalla. 2020. "Synthesis of Mg–Zn–Nd Master Alloy in Metallothermic Reduction of Neodymium from Fluoride–Chloride Melt" Crystals 10, no. 11: 985. https://doi.org/10.3390/cryst10110985

APA Style

Beloglazov, I., Savchenkov, S., Bazhin, V., & Kawalla, R. (2020). Synthesis of Mg–Zn–Nd Master Alloy in Metallothermic Reduction of Neodymium from Fluoride–Chloride Melt. Crystals, 10(11), 985. https://doi.org/10.3390/cryst10110985

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