LOW-OXYGEN ALSC ALLOY POWDERS AND METHOD FOR THE PRODUCTION THEREOF

Abstract

An alloy powder which has a composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y. The allow powder has purity of 99% by weight or more, based on metallic impurities, and an oxygen content of less than 0.7% by weight, based on a total weight of the alloy powder, as determined by a carrier gas hot extraction.

Claims

1-15. (canceled)

16. An alloy powder comprising: a composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y; a purity of 99% by weight or more, based on metallic impurities; and an oxygen content of less than 0.7% by weight, based on a total weight of the alloy powder, as determined by a carrier gas hot extraction.

17. The alloy powder as recited in claim 16, further comprising: a chlorine content of less than 1000 ppm, as determined by an ion chromatography.

18. The alloy powder as recited in claim 16, wherein the alloy powder has an X-ray diffraction pattern which has no reflections of compounds selected from the group consisting of Sc.sub.2O.sub.3, ScOCl, ScCl.sub.3, Sc, Al.sub.2O.sub.3, X.sub.3ScF.sub.6, XScF.sub.4, ScF.sub.3 and other oxidic and fluoridic foreign phases thereof, where X is a sodium ion or a potassium ion.

19. The alloy powder as recited in claim 16, further comprising: a magnesium content of less than 5000 ppm, as determined by an ICP-OES.

20. The alloy powder as recited in claim 16, further comprising: a particle size distribution D90 of less than 2 mm, as determined in accordance with ASTM B 822-10.

21. The alloy powder as recited in claim 16, further comprising: a fluoride content of less than 1000 ppm, as determined by an ion chromatography.

22. A process for producing the alloy powder as recited in claim 16, the process comprising: reacting a scandium source with an aluminum metal or with an aluminum salt in the presence of a reducing agent to give Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y.

23. The process as recited in claim 22, wherein the scandium source is selected from the group consisting of Sc.sub.2O.sub.3, ScOCl, ScCl.sub.3, ScCl.sub.3*6H.sub.2O, ScF.sub.3, X.sub.3ScF.sub.6, XScF.sub.4, and mixtures thereof, where X is a potassium ion or a sodium ion.

24. The process as recited in claim 22, wherein the reducing agent is selected from the group consisting of magnesium, calcium, lithium, sodium and potassium.

25. The process as recited in claim 22, wherein the aluminum metal and magnesium, as the reducing agent, are reacted in the form of an Al/Mg alloy with the scandium source to give Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y.

26. The process as recited in claim 25, wherein at least one of the aluminum metal and the Al/Mg alloy are present in the form of a powder,

27. The process as recited in claim 26, wherein the powder has, an average particle size D50 of greater than 40 μm, and an average particle size D90 of greater than 300 μm, each being determined in accordance with ASTM B822-10.

28. The process as recited in claim 22, wherein, the scandium source is a scandium fluoride salt, and the reducing agent is sodium or potassium, so that the scandium fluoride salt as the scandium source is reacted with an aluminum metal or with an aluminum salt in the presence of sodium or potassium as the reducing agent to give Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y.

29. The process as recited in claim 22, wherein the reaction is carried out at a temperature of from 400 to 1050° C.

30. An alloy powder having a composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y, which is obtained by the process as recited in claim 22.

31. A method of using the alloy powder as recited in claim 16 in an electronic component in an electronics industry, the method comprising: providing the alloy powder as recited in claim 16; and using the alloy powder in an electronic component.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] The present invention is described in greater detail below on the basis of embodiments and of the drawings in which:

[0019] FIG. 1 shows an X-ray diffraction pattern of the ScCl.sub.3 precursor P2;

[0020] FIG. 2 shows an X-ray diffraction pattern of the ScCl.sub.3 precursor P3;

[0021] FIG. 3 shows an X-ray diffraction pattern of the AlSc alloy powder of Comparative Example C5;

[0022] FIG. 4 shows an X-ray diffraction pattern of the AlSc alloy powder of Example E7 according to the present invention; and

[0023] FIG. 5 shows an X-ray diffraction pattern of the AlSc alloy powder of Example E13 according to the present invention.

DETAILED DESCRIPTION

[0024] The present invention therefore firstly provides an alloy powder having the composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9 and x=1−y, determined via X-ray fluorescence analyses (XRF), and having a purity of 99% by weight or more, based on metallic impurities, wherein the alloy powder has an oxygen content of less than 0.7% by weight, based on the total weight of the powder, determined via carrier gas hot extraction.

[0025] In a particular embodiment, the alloy powder of the present invention has a composition Al.sub.xSc.sub.y, where 0.2≤y≤0.8, for example, 0.24≤y≤0.7, in each case with x=1−y, determined via X-ray fluorescence analyses (XRF). The alloy powder can also comprise mixtures of Al.sub.xSc.sub.y of different compositions. The alloy powder of the present invention can, for example, have the composition Al.sub.3Sc (x=0.75; y=0.25) or Al.sub.2Sc (x=2/3; y=1/3) and any mixtures thereof.

[0026] In a further embodiment, the alloy powder of the present invention can, for example, have a purity of 99.5% or more, for example, 99.9% by weight or more, in each case based on the metallic impurities.

[0027] The powder of the present invention is in particular characterized by its low oxygen content. The alloy powder can, for example, have an oxygen content of less than 0.5% by weight, for example, less than 0.1% by weight, for example, less than 0.05% by weight, in each case based on the total weight of the powders. The oxygen content of the powder can be determined via carrier gas hot extraction.

[0028] It has surprisingly been found that the powders of the present invention are particularly suitable for applications in which a high purity is required. Apart from the low oxygen content, it has surprisingly been found that the powder also has the low chloride content which is essential for the electronics industry. For this reason, in an embodiment, the alloy powder of the present invention can, for example, have a chlorine content of less than 1000 ppm, for example, less than 400 ppm, for example, less than 200 ppm, in particular less than 50 ppm, as determined via ion chromatography.

[0029] For the purposes of the present invention, “ppm” in each case means parts per million based on the total weight of the powder.

[0030] It has in practice been found that, in particular, metallic scandium and oxidic and halogen-containing impurities lead to difficulties in further processing; these impurities can generally be detected via X-ray diffraction. These impurities are not only oxidic compounds of scandium, e.g., Sc.sub.2O.sub.3 and ScOCl, but also oxidic impurities which are introduced via the reactants used. In an embodiment of the present invention, an X-ray diffraction pattern of the alloy powder of the present invention does not, for example, have any reflections of compounds selected from the group consisting of Sc.sub.2O.sub.3, ScOCl, ScCl.sub.3, Sc, X.sub.3ScF.sub.6, XScF.sub.4, ScF.sub.3 and other oxidic impurities and fluoridic foreign phases, where X is a potassium or sodium ion. The other oxidic impurities can, for example, be MgO, Al.sub.2O.sub.3, CaO and/or MgAl.sub.2O.sub.4.

[0031] In an embodiment, the alloy powder of the present invention can, for example, also have a magnesium content of less than 5000 ppm, for example, less than 2500 ppm, for example, less than 500 ppm, in particular less than 100 ppm, as determined via ICP-OES. In an embodiment, the alloy powder of the present invention can, for example, also have a content of calcium of less than 5000 ppm, for example, less than 2500 ppm, for example, less than 500 ppm, in particular less than 100 ppm, as determined via ICP-OES. In a further embodiment, the alloy powder of the present invention can, for example, have a content of sodium of less than 5000 ppm, for example, less than 2500 ppm, for example, less than 500 ppm, in particular less than 100 ppm, as determined via ICP-OES. For the purposes of the present invention, the terms “magnesium content”, “sodium content”, and “calcium content” encompass both the elements and the ions.

[0032] In an embodiment, the alloy powder of the present invention can, for example, also have a fluorine content of less than 1000 ppm, for example, less than 400 ppm, for example, less than 200 ppm, in particular less than 50 ppm, as determined via ion chromatography.

[0033] The alloy powder of the present invention is particularly suitable for further processing in the electronics industry, for example, as a precursor for the production of sputtering targets and also for the dielectrics layers produced therefrom, with not only a high purity, but also with the appropriate particle size here being of importance. For this reason, an embodiment of the alloy powder can, for example, have a particle size D90 of less than 2 mm, for example, from 100 μm to 1 mm, for example, from 150 μm to 500 μm, as determined in accordance with ASTM B822-10. The D90 of the particle size distribution is the particle size for which 90% by volume of the particles have a particle size equal to or smaller than the value indicated.

[0034] The present patent application further provides a process for producing the alloy powder of the present invention, where a scandium source is reacted with aluminum metal or an aluminum salt in the presence of a reducing agent to provide Al.sub.xSc.sub.y, where 0.1≤y≤0.9, for example, 0.2≤y≤0.8, for example, 0.24≤y≤0.7, in each case with x=1−y. According to the present invention, the reducing agent is different from aluminum or an aluminum salt and does not comprise any aluminum. The aluminum salt can, for example, be a salt selected from the group consisting of X.sub.3AlF.sub.6, XAlF.sub.4, AlF.sub.3, AlCl.sub.3, where X is a potassium or sodium ion. It has surprisingly been found that the formation of undesirable oxidic impurities can be avoided or significantly reduced by the process of the present invention and that AlSc alloy powders having a high purity and a low oxygen content are obtainable in this way.

[0035] While recourse must usually be made to ScCl.sub.3 or Sc metal produced in a costly manner as a starting material in conventional production processes, the process of the present invention is characterized by the reaction also being able to occur starting from the oxides and oxychlorides of scandium and starting from ScCl.sub.3 contaminated with ScOCl and/or Sc.sub.2O.sub.3, making the complicated dehydration or purification of the starting material, as described in the prior art, superfluous. In an embodiment of the process of the present invention, the scandium source can, for example, be selected from the group consisting of Sc.sub.2O.sub.3, ScOCl, ScCl.sub.3, ScCl.sub.3*6H.sub.2O, ScF.sub.3, X.sub.3ScF.sub.6, XScF.sub.4, and mixtures of these compounds, where X is a potassium or sodium ion.

[0036] Alkali metals and alkaline earth metals have in particular been found to be suitable reducing agents in the process of the present invention. In an embodiment, the reducing agent can, for example, therefore be selected from the group consisting of lithium, sodium, potassium, magnesium and calcium, with, according to the present invention, in particular sodium and potassium being used in the reaction of the fluorides of scandium and magnesium and calcium being used in the reaction of the chlorides of scandium. The use of the reducing agents indicated has the advantage that the oxidation products of the reducing agent which are formed in the reduction, for example, MgO, MgCl.sub.2 and NaF, can be easily removed by washing. In an embodiment, the process can, for example, further comprise a step in which the alloy powder obtained is washed. Distilled water and/or dilute mineral acids such as H.sub.2SO.sub.4 and HCl can, for example, be used for washing the powder.

[0037] It has surprisingly been found that the introduction of impurities can be reduced further when the reducing agent is introduced in the form of vapour. For this reason, an embodiment can, for example, provide that the reducing agent be used in the form of vapour.

[0038] It has found to be particularly effective for ScCl.sub.3, ScOCl and/or Sc.sub.2O.sub.3 or mixtures thereof as the scandium source to be reacted with aluminum metal and magnesium as the reducing agent. It has here surprisingly been found that the purity of the AlSc alloy powder obtained can be increased further when the aluminum metal and the magnesium are prealloyed before the reaction. In an embodiment of the process of the present invention, aluminum metal and magnesium in the form of an Al/Mg alloy can, for example, be reacted with ScCl.sub.3, ScOCl and/or Sc.sub.2O.sub.3 or mixtures thereof to provide Al.sub.xSc.sub.y, where 0.1≤y≤0.9, for example, 0.2≤y≤0.8, for example, 0.24≤y≤0.7, in each case with x=1−y.

[0039] It has been found to be particularly advantageous for the aluminum metal and/or the Al/Mg alloy to be used in the form of a coarse powder, since the introduction of surface oxygen from these starting materials is thereby decreased and the oxygen contents of the alloy powder obtained can thereby be decreased further. In an embodiment, the aluminum metal and/or the Al/Mg alloy can, for example, be present in the form of a powder, where the powder can, for example, have an average particle size D50 of greater than 40 μm, for example, from 100 μm to 600 μm, and has a D90 of greater than 300 μm, for example, from 500 μm to 2 mm, as determined via ASTM B822-10. The D90 value of the particle size distribution is the particle size for which 90% by volume of the particles have a size which is equal to or less than the value indicated; correspondingly, the D50 value is the particle size for which 50% by volume of the particles have a size which is equal to or less than the value indicated.

[0040] In an embodiment, the process of the present invention can, for example, be carried out at significantly lower temperatures than are customary in the prior art, as a result of which inclusions of the oxidized reducing agent, for example, MgCl.sub.2 or MgO, in the alloy powder can be avoided and the purity of the powder can thereby be increased. This applies particularly to the use of Al/Mg alloy because of the melting point lowering in alloy formation from Al and Mg which is here observed. In an embodiment of the process of the present invention, the reaction can, for example, be carried out at a temperature of from 400 to 1050° C., for example, from 400 to 850° C., for example, from 400 to 600° C. The reaction time here can, for example, be from 0.5 to 30 hours, for example, from 1 to 24 hours.

[0041] Particularly in cases in which aluminum metal and magnesium are used together with ScCl.sub.3 as scandium source, it has been found to be advantageous for the reactants to be vaporized separately and then combined in the form of vapour in a reaction space. In this way, the oxidic impurities of the starting material can be separated off before the reaction. In an embodiment, ScCl.sub.3 and also aluminum metal and magnesium can, for example, be vaporized separately and then combined in the gaseous state in a reaction space and reacted to give an alloy powder having the composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9, for example, 0.2≤y≤0.8, for example, 0.24≤y≤0.7, in each case with x=1−y.

[0042] It has surprisingly been found in the context of the present invention that the AlSc alloy powders of the present invention are also obtainable from the fluoride salts of scandium. In an alternative embodiment of the process of the present invention, a scandium fluoride salt can, for example, be reacted together with aluminum metal or an aluminum salt in the presence of sodium or potassium to give an alloy powder having the composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9, for example, 0.2≤y≤0.8, for example, 0.24≤y≤0.7, in each case with x=1−y. The scandium fluoride salt can, for example, be selected from the group consisting of ScF.sub.3, XScF.sub.4, X.sub.3ScF.sub.6, and any combinations thereof, where X is potassium or sodium or a mixture thereof. The aluminum salt can, for example, be selected from the group consisting of AlF.sub.3, X.sub.3AlF.sub.6 and XAlF.sub.4, where X is a potassium or sodium ion.

[0043] The reduction can here be carried out either with intermingled reducing agents or with vaporous reducing agents. The reduction can also be carried out within a melt. The advantage of these alternatives according to the present invention is that the fluorides of scandium, unlike the chlorides, are stable and less hygroscopic in air and can be obtained by precipitation from aqueous solutions. They can therefore be handled in air, which makes their use in industrial processes considerably easier.

[0044] The process of the present invention allows for the production of particularly pure AlSc alloy powders which have a low oxygen content. The present invention therefore further provides an alloy powder having the composition Al.sub.xSc.sub.y, where 0.1≤y≤0.9, for example, 0.2≤y≤0.8, for example, 0.24≤y≤0.7, in each case with x=1−y, as determined via X-ray fluorescence analyses (XRF), obtainable by the process of the present invention. The powder which can be obtained in this way can, for example, have an oxygen content of less than 0.7% by weight, for example, less than 0.5% by weight, for example, less than 0.1% by weight, and in particular less than 0.05% by weight, in each case based on the total weight of the powder and determined via carrier gas hot extraction. The powder obtained in this can, for example, have the above-described properties.

[0045] The alloy powders of the present invention have a high purity and low oxygen content and are therefore particularly suitable for use in the electronics industry. The present invention therefore further provides for the use of the alloy powder of the present invention in the electronics industry or in electronic components, in particular for the production of sputtering targets and BAW filters.

[0046] The present invention will be illustrated with the aid of the following examples, but these should in no event be interpreted as a restriction of the inventive concept.

EXAMPLES

1. Production of the Scandium Sources ScCl.SUB.3 .and ScOCl Used (Precursors P1 to P5)

[0047] ScCl.sub.3 was produced in a manner analogous to the prior art summarized Table 1. Here, ScCl.sub.3*6H.sub.2O (purity Sc.sub.2O.sub.3/TREO 99.9%), obtainable from Shinwa Bussan Kaisha, Ltd., served as the starting material in each case.

[0048] P1: In the case of P1, the reaction was carried out at 720° C. in a stream of argon without addition of NH.sub.4Cl for 2 hours.

[0049] P2: P2 is based on Example 2 of EP 0 395 472 A1, but the NdCl.sub.3*6H.sub.2O described there was replaced by the corresponding Sc compound, ScCl.sub.3*6H.sub.2O.

[0050] P3: P3 is based on Example 5 of CN 110540117 A, but the mixture of LaCl.sub.3*7H.sub.2O/CeCl.sub.3*7H.sub.2O described there was replaced by the corresponding hydrate ScCl.sub.3*6H.sub.2O.

[0051] P4: As P4, use was made of phase-pure ScOCl which was produced by the thermal treatment of ScCl.sub.3*6H.sub.2O in a stream of HCl gas in a fused silica tube at 900° C. for 2 hours without addition of NH.sub.4Cl.

[0052] P5: As P5, use was made of Sc.sub.2O.sub.3 (purity Sc.sub.2O.sub.3/TREO 99.9%) obtainable from Shinwa Bussan Kaisha, Ltd.

[0053] The phase compositions determined from the X-ray diffraction pattern (XRD) for the respective products and also oxygen contents and residual contents of H.sub.2O are likewise reported in Table 1.

2. Comparative Experiments C1 to C7

[0054] For the comparative experiments C1 to C6, the scandium-containing precursors P1 to P5 were mixed as indicated in Table 2 with aluminum or magnesium powder and introduced into a ceramic crucible. The average particle size D50 of the aluminum powder used was 520 μm and that of the magnesium powder used was 350 μm. A thermal reaction in an argon atmosphere was subsequently carried out as indicated in Table 2. The respective reaction products were subsequently washed with dilute sulfuric acid, dried in a convection drying oven for at least 10 hours, and subsequently subjected to chemical analysis and X-ray diffraction examination. The results are likewise reported in Table 2.

[0055] For comparative experiment C7, Example 2 of WO 2014/138813 A1 was replicated using the precursor P3 (ScCl.sub.3) and an aluminum powder having an average particle size D50 of 14 μm. After the reaction under conditions analogous to those there disclosed, a powder having the following properties was obtained:

[0056] X-ray diffraction (XRD): Al.sub.3Sc

[0057] Chemical analysis: oxygen 0.81% by weight, C1 15000 ppm, F<50 ppm, Mg<10 ppm, Na<10 ppm, Ca<10 ppm

[0058] X-ray fluorescence analysis (XRF): Al:Sc ratio=0.77:0.23

[0059] Particle size D50: 25 μm

[0060] The total of all metallic impurities (including Mg, Ca and Na) was found to be <500 ppm for all experiments.

3. Experiments According to the Present Invention

[0061] a) E1 to E8

[0062] In a manner analogous to the comparative experiments C1 to C7, scandium-containing precursors P1 to P5 were mixed as indicated in Table 3 with pulverulent Al and Mg or an Al/Mg alloy (69% by weight of Al, 31% by weight of Mg) and introduced into ceramic crucibles for experiments E1 to E8. The average particle size D50 of the aluminum powder used was 520 μm, that of the magnesium powder was 350 μm, and that of the Al/Mg alloy was 380 μm. The thermal reactions were carried out within a steel retort through which argon was passed during the entire reaction time, as indicated in Table 3. The respective reaction products were subsequently washed with dilute sulfuric acid, dried in a convection drying oven for at least 10 hours, and subsequently subjected to chemical analysis and X-ray diffraction examination. The results are likewise reported in Table 3. The sodium and calcium content was in each case <10 ppm in all experiments. The total of all metallic impurities (including Mg, Ca and Na) was found to be <400 ppm in all experiments.

[0063] b) Experiments E9 to E34

[0064] The scandium- and aluminum-containing precursors were used in the ratios indicated in Table 3 and Table 4 and distributed over a finely perforated niobium sheet. This was located in a steel reduction vessel which had been filled with the amount of sodium required for the reaction plus an excess of 50% based on the stoichiometry. The niobium sheet was placed above the sodium and without direct contact with the sodium. The reaction was carried out within a steel retort through which argon was passed during the entire reaction time. The sodium was vaporized, as a result of which the precursors were reduced to elemental Sc and Al which were reacted in situ to give the target alloy.

[0065] After the reaction, the retort was carefully passivated with air and the steel reduction vessel was then removed. Sodium fluoride formed during the reaction was washed out of the reaction product using water, and the product was then dried at low temperatures. The calcium content was <10 ppm and the sodium content <50 ppm for all experiments. The total of all metallic impurities (including Mg, Ca and Na) was found to be <400 ppm for all experiments.

[0066] c) Experiments E35 to E42

[0067] The scandium- and aluminum-containing precursors were mixed (see Table 4) and introduced together with the amount of sodium required for the reaction, plus an excess of 5% based on the stoichiometry, into a niobium vessel. The reaction was carried out within a steel retort through which argon was passed during the entire reaction time. The precursors were reduced by the sodium to elemental Sc and Al which were reacted in situ to give the target alloy.

[0068] After the reaction, the retort was carefully passivated with air and the steel reduction vessel was then removed. Excess sodium was dissolved by reaction with ethanol and the remaining solid was washed with water. The sodium fluoride and/or sodium chloride was here washed out of the reaction product, and the product was then dried at low temperatures. The calcium content was <10 ppm for all experiments and the sodium content was <50 ppm. The total of all metallic impurities (including Mg, Ca and Na) was found to be <400 ppm for all experiments.

[0069] The oxygen content of the powders was determined via carrier gas hot extraction (Leco TCH600) and the particle sizes D50 and D90 were each determined via laser light scattering (ASTM B822-10, MasterSizer S, dispersion in water and Daxad 11.5 min ultrasonic treatment). Trace analysis of the metallic impurities was carried out via ICP-OES (optical emission spectroscopy with inductively coupled plasma) using the following analytical instruments PQ 9000 (Analytik Jena2) or Ultima 2 (Horiba) and the determination of the composition of the crystalline phases was carried out on pulverulent samples via X-ray diffraction (XRD) using an instrument from Malvern-PANalytical (X'Pert-MPD Pro with semiconductor detector, X-ray tubes Cu LFF with 40 KV/40 mA, Ni filter). The determination of the halides F and Cl was based on ion chromatography (ICS 2100). The instruments Axios and PW2400 from Malvern-PANalytical served for X-ray fluorescence analyses (XRF) of Al and Sc.

[0070] All contents of chemical elements reported in % are % by weight and are in each case based on the total weight of the powder. The purity in % by weight, in each case based on the metallic impurities, is the subtraction of all metallic impurities determined in % by weight from the 100% ideal value. The Al:Sc ratio is calculated from the contents of Al and Sc determined via XRF.

[0071] The abbreviation TREO stands for the total oxides of rare earth elements.

TABLE-US-00001 TABLE 1 Production of ScCl.sub.3 Precursors Experiment Target Product Product Product number product Prior art Production XRD O [%] Residual H.sub.2O [%] P1 ScCl.sub.3 W. W. Wendlandt Heating ScCl.sub.3*6H.sub.2O to 720° C. in a stream of ScOCl, ScCl.sub.3 7.1 0.5 et al argon without addition of NH.sub.4Cl P2 ScCl.sub.3 EP 0395472 A1 Analogous to Example 2, but ScCl.sub.3*6H.sub.2O ScCl.sub.3, ScClO 2.5 0.03 instead of NdCl.sub.3*6H.sub.2O P3 ScCl.sub.3 CN 110540117 A Analogous to Example 5, but ScCl.sub.3*6H.sub.2O ScCl.sub.3 0.09 0.003 instead of LaCl.sub.3*7H.sub.2O/CeCl.sub.3*7H.sub.2O mixture

TABLE-US-00002 TABLE 2 Comparative Examples for the Production of AlSc Alloy Powders Al/Mg alloy 69% by weight of Al/ Amount 31% by Product Sc of Sc weight Reaction Reaction Product XRF Product Product Product Product Experiment precursor precursor Al Mg of Mg temperature time XRD Al:Sc O C F Mg number production [g] [g] [g] [g] [° C.] [h] Result ratio [%] ppm ppm ppm C1 Sc.sub.2O.sub.3 200 0 210 0 950 3 Sc.sub.2O.sub.3 not able to be 35.0    <50 <50 480 (P5) determined C2 Sc.sub.2O.sub.3 200 640 0 0 950 3 Sc.sub.2O.sub.3 not able to be 34.9   <50 <50 <10 (P5) determined C3 ScClO 200 640 0 0 950 3 ScClO not able to be 16.0   370 000 <50 <10 from P4 determined C4 ScCl.sub.3 200 220 0 0 800 3 Al.sub.3Sc + — 4.1    27 000 <50 <10 from P1 ScClO   C5 ScCl.sub.3 200 220 0 0 800 3 Al.sub.3Sc + — 2.2    33 000 <50 <10 from P2 ScClO   C6 ScCl.sub.3 200 220 0 0 800 3 Al.sub.3Sc 0.77:0.23 0.75    12 000 <50 <10 from P3

TABLE-US-00003 TABLE 3 Examples According to the Present Invention for Production of AlSc Alloy Powders from ScCl.sub.3 Precursors Al/Mg alloy 69% by weight of Al/ 31% Reac- by tion Sc Amount weight tem- Reac- Product precursor of Sc of pera- tion Product XRF Product Product Product Product Product Experi- produc- precursor Al Mg Mg Na ture time XRD Al:Sc O Cl F Mg D90 ment tion [g] [g] [g] [g] [g] [ºC] [h] Result ratio [%] ppm ppm ppm μm E1 Sc.sub.2O.sub.3 200 0 0 680 0 mixed 500 3 Al.sub.3Sc 0.75:0.25 0.590 <50 <50 <10 202 from P5 E2 ScClO 200 0 0 680 0 mixed 500 3 Al.sub.3Sc 0.75:0.25 0.489 180 <50 <10 180 from P4 E3 ScCl.sub.3 200 220 100 0 0 mixed 800 3 Al.sub.3Sc 0.75 0.25 0.410 185 <50 266 420 from P1 E4 ScCl.sub.3 200 0 0 320 0 mixed 500 3 Al.sub.3Sc 0.75:0.25 0.095 <50 <50 25 168 from P1 E5 ScCl.sub.3 200 220 100 0 0 mixed 800 3 Al.sub.3Sc 0.75:0.25 0.310 168 <50 401 550 from P2 E6 ScCl.sub.3 200 220 100 0 0 mixed 800 3 Al.sub.3Sc 0.75:0.25 0.078 128 <50 330 430 from P3 E7 ScCl.sub.3 200 220 100 0 0 mixed 670 3 Al.sub.3Sc 0.75:0.25 0.049 <50 <50 94 358 from P3 E8 ScCl.sub.3 200 0 0 320 0 mixed 500 3 Al.sub.3Sc 0.74:0.26 0.033 <50 <50 35 210 from P3 E9 ScCl.sub.3 200 107 0 0 137 gaseous 750 4 Al.sub.3Sc 0.75:0.25 0.048 <50 <50 <10 290 from P2 E10 ScCl.sub.3 200 107 0 0 137 gaseous 750 4 Al.sub.3Sc 0.75:0.25 0.078 <50 <50 <10 277 from P1 E11 ScCl.sub.3 200 107 0 0 137 gaseous 750 4 Al.sub.3Sc 0.75:0.25 0.038 <50 <50 <10 250 from P3 E12 ScCl.sub.3 200 89 0 0 137 gaseous 750 4 Al.sub.2Sc. 0.72:0.28 0.069 <50 <50 <10 233 from P3 Al.sub.3Sc E13 ScCl.sub.3 200 98 0 0 137 gaseous 750 4 Al.sub.2Sc, 0.73:0.27 0.046 <50 <50 <10 231 from P3 Al.sub.3Sc E14 ScCl.sub.3 200 80 0 0 137 gaseous 750 4 Al.sub.2Sc, 0.69:0.31 0.105 <50 <50 <10 241 from P3 Al.sub.3Sc

TABLE-US-00004 TABLE 4 Examples According to the Present Invention for Production of AlSc Alloy Powders from Sc Fluorides Sc Amount Amount Reaction Reac- Product precursor of Sc of Al tempera- tion Product XRF Product Product Product Product Product Experi- produc- precursor precursor Na ture time XRD Al:Sc O Cl F Mg D90 ment tion [g] g [g] [ºC] [h] Result ratio [%] ppm ppm ppm μm E15 Na.sub.3ScF.sub.6/ 200 550 363 gaseous 750 4 Al.sub.3Sc 0.75:0.25 0.097 <50 <100 <10 240 Na.sub.3AlF.sub.6 Na3ScF.sub.6 Na.sub.3AlF.sub.6 E16 Na.sub.3ScF.sub.6/ 200 370 271 gaseous 750 4 Al.sub.2Sc 0.66:0.34 0.189 <50 <100 <10 280 Na.sub.3AlF.sub.6 Na.sub.3ScF.sub.6 Na.sub.3AlF.sub.6 E17 Na.sub.3ScF.sub.6/ 200 460 317 gaseous 750 4 Al.sub.2Sc. 0.72:0.28 0.102 <50 <100 <10 301 Na.sub.3AlF.sub.6 Na.sub.3ScF.sub.6 Na.sub.3AlF.sub.6 Al.sub.3Sc E18 Na.sub.3ScF.sub.6/ 200 505 340 gaseous 750 4 Al.sub.2Sc. 0.74:0.26 0.150 <50 <100 <10 250 Na.sub.3AlF.sub.6 Na.sub.3ScF.sub.6 Na.sub.3AlF.sub.6 Al.sub.3Sc E19 Na.sub.3ScF.sub.6/ 200 415 294 gaseous 750 4 Al.sub.2Sc. 0.68:0.32 0.209 <50 <100 <10 260 Na.sub.3AlF.sub.6 Na.sub.3ScF.sub.6 Na.sub.3AlF.sub.6 Al.sub.3Sc E20 AlF.sub.3/ScF.sub.3 200 495 811 gaseous 750 4 Al.sub.3Sc 0.74:0.26 0.044 <50 <100 <10 180 ScF.sub.3 AlF.sub.3 E21 AlF.sub.3/ScF.sub.3 200 330 609 gaseous 750 4 Al.sub.2Sc 0.65:0.35 0.204 <50 <100 <10 153 ScF.sub.3 AlF.sub.3 E22 AlF.sub.3/ScF.sub.3 200 415 710 gaseous 750 4 Al.sub.2Sc. 0.73:0.27 0.134 <50 <100 <10 181 ScF.sub.3 AlF.sub.3 Al.sub.3Sc E23 AlF.sub.3/ScF.sub.3 200 455 760 gaseous 750 4 Al.sub.2Sc. 0.75:0.25 0.072 <50 <100 <10 145 ScF.sub.3 AlF.sub.3 Al.sub.3Sc E24 AlF.sub.3/ScF.sub.3 200 375 660 gaseous 750 4 Al.sub.2Sc. 0.69:0.31 0.133 <50 <100 <10 175 ScF.sub.3 AlF.sub.3 Al.sub.3Sc E25 Na.sub.3ScF.sub.6/Al 200  70 91 gaseous 750 4 Al.sub.3Sc 0.73:0.27 0.048 <50 <100 <10 350 Na.sub.3ScF.sub.6 Al E26 Na.sub.3ScF.sub.6/Al 200  47 91 gaseous 750 4 Al.sub.2Sc 0.69:0.31 0.292 <50 <100 <10 365 Na.sub.3ScF.sub.6 A E27 Na.sub.3ScF.sub.6/Al 200  58 91 gaseous 750 4 Al.sub.2Sc. 0.72:0.28 0.185 <50 <100 <10 342 Na.sub.3ScF.sub.6 Al Al.sub.3Sc E28 Na.sub.3ScF.sub.6/Al 200  53 91 gaseous 750 4 Al.sub.2Sc. 0.74:0.26 0.064 <50 <100 <10 329 Na.sub.3ScF.sub.6 Al Al.sub.3Sc E29 Na.sub.3ScF.sub.6/Al 200  64 91 gaseous 750 4 Al.sub.2Sc. 0.69:0.31 0.306 <50 <100 <10 335 Na.sub.3ScF.sub.6 Al Al.sub.3Sc E30 NaScF.sub.4/Al 200 123 144 gaseous 750 4 Al.sub.3Sc 0.74:0.26 0.032 <50 <100 <10 201 Na.sub.3ScF.sub.6 Al E31 NaScF.sub.4/Al 200  82 144 gaseous 750 4 Al.sub.2Sc 0.64:0.36 0.288 <50 <100 <10 185 Na.sub.3ScF.sub.6 Al E32 NaScF.sub.4/Al 200 103 144 gaseous 750 4 Al.sub.2Sc. 0.7:0.3 0.159 <50 <100 <10 189 Na.sub.3ScF.sub.6 Al Al.sub.3Sc E33 NaScF.sub.4/Al 200 113 144 gaseous 750 4 Al.sub.2Sc. 0.75:0.25 0.044 <50 <100 <10 209 Na.sub.3ScF.sub.6 A1 Al.sub.3Sc E34 NaScF.sub.4/Al 200  93 144 gaseous 750 4 Al.sub.2Sc. 0.71:0.29 0.233 <50 <100 <10 195 Na.sub.3ScF.sub.6 Al Al.sub.3Sc E35 Na.sub.3ScF.sub.6/ 200 550 254 mixed 750 4 Al.sub.3Sc 0.75:0.25 0.120 <50 <100 <10 112 Na.sub.3AlF.sub.6 Na.sub.3ScF.sub.6 Na.sub.3AlF.sub.6 E36 Na.sub.3ScF.sub.6/ 200 370 190 mixed 750 4 Al.sub.2Sc 0.64:0.36 0.381 <50 <100 <10 131 Na.sub.3AlF.sub.6 Na.sub.3ScF.sub.6 Na.sub.3AlF.sub.6 E37 AlF.sub.3/ScF.sub.3 200 495 568 mixed 750 4 Al.sub.3Sc 0.75:0.25 0.136 <50 <100 <10 260 ScF AlF.sub.3 E38 AlF.sub.3/ScF.sub.3 200 330 426 mixed 750 4 Al.sub.2Sc 0.69:0.31 0.299 <50 <100 <10 251 ScF.sub.3 AlF.sub.3 E39 NaScF.sub.4/Al 200  70 64 mixed 750 4 Al.sub.3Sc 0.74:0.26 0.211 <50 <100 <10 321 Na.sub.3ScF.sub.6 Al E40 NaScF.sub.4/Al 200  47 64 mixed 750 4 Al.sub.2Sc 0.65:0.35 0.273 <50 <100 <10 309 Na.sub.3ScF.sub.6 Al E41 NaScF.sub.4/Al 200 123 101 mixed 750 4 Al.sub.3Sc 0.76:0.24 0.085 <50 <100 <10 150 Na.sub.3ScF.sub.4 Al E42 NaScF.sub.4/Al 200  82 101 mixed 750 4 Al.sub.2Sc 0.68:0.32 0.349 <50 <100 <10 179 Na.sub.3ScF.sub.4 Al

[0072] As can be seen from the data in Tables 3 and 4, the alloy powders of the present invention are distinguished not only by a low oxygen content, but also by a low chlorine and fluorine content, which is not achieved using the processes described in the prior art. The experiments presented also show that the process of the present invention also allows the production of high-purity AlSc alloy powder proceeding from the oxides, fluorides and chlorides of scandium, so that a complicated work-up of the starting materials can be dispensed with.

[0073] The X-ray diffraction patterns of the two AlSc alloy powders according to the present invention which are depicted are representative of all experiments E1 to E42 according to the present invention which have been described. As can be seen from a comparison of the patterns provided, the patterns of the powders according to the present invention do not show any further reflections in addition to those of the desired AlSc target compound.

[0074] The present invention is not limited to embodiments described herein; reference should be had to the appended claims.