METHOD FOR EXTRACTING ALUMINUM
20260110053 ยท 2026-04-23
Assignee
Inventors
Cpc classification
B33Y70/00
PERFORMING OPERATIONS; TRANSPORTING
B22F2998/10
PERFORMING OPERATIONS; TRANSPORTING
C22B5/02
CHEMISTRY; METALLURGY
B22F9/04
PERFORMING OPERATIONS; TRANSPORTING
International classification
B22F9/04
PERFORMING OPERATIONS; TRANSPORTING
B33Y70/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A method for extracting aluminum according to one embodiment of the present disclosure comprises a hydrogenation reaction step of an aluminum (Al) alloy; a separation step of NaAlH.sub.4 generated from the hydrogenation reaction step; a dehydrogenation reaction step of the NaAlH.sub.4; and a pure aluminum extraction step.
Claims
1. A method for extracting aluminum comprising: a hydrogenation reaction step of an aluminum (Al) alloy; a separation step of NaAlH.sub.4 generated from the hydrogenation reaction step; a dehydrogenation reaction step of the NaAlH.sub.4; and a pure aluminum extraction step.
2. The method for extracting aluminum of claim 1, wherein in the hydrogenation reaction step, the aluminum alloy reacts with sodium hydride (NaH).
3. The method for extracting aluminum of claim 1, wherein in the separation step of NaAlH.sub.4, the NaAlH.sub.4 is dissolved in a solvent.
4. The method for extracting aluminum of claim 3, wherein the solvent dissolves only NaAlH.sub.4.
5. The method for extracting aluminum of claim 3, wherein the solvent is one or more of tetrahydrofuran (THF), dioxane, acetone, dimethyl sulfoxide (DMSO), dimethylformamide (DMF), 1-methyl-2-pyrrolidone (NMP), or any combination thereof.
6. The method for extracting aluminum of claim 1, wherein in the separation step of NaAlH.sub.4, the NaAlH.sub.4 is dissolved in a solvent to create a dissolved NaAlH.sub.4 solution, and wherein the method further comprises heating the dissolved NaAlH.sub.4 solution.
7. The method for extracting aluminum of claim 1, wherein the dehydrogenation reaction step comprises: heating the NaAlH.sub.4 at a first temperature; and separating remaining NaAlH.sub.4 and NaH.
8. The method for extracting aluminum of claim 7, wherein the first temperature is 95 C. or higher.
9. The method for extracting aluminum of claim 7, wherein the dehydrogenation reaction step further comprises recapturing NaH and H.sub.2.
10. The method for extracting aluminum of claim 1, wherein the dehydrogenation reaction step comprises: heating the NaAlH.sub.4 at a second temperature; and supplying hydrogen.
11. The method for extracting aluminum of claim 10, wherein the second temperature is a sodium (Na) evaporation temperature or higher.
12. The method for extracting aluminum of claim 10, wherein the second temperature is 882 C. or higher.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] The above and other aspects, features, and advantages of the present disclosure should become apparent from the detailed description of the following aspects in conjunction with the accompanying drawings, in which:
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
DETAILED DESCRIPTION
[0029] Hereinafter, examples of the present disclosure are described in detail with reference to the accompanying drawings. Like or similar reference numerals designate like or similar elements in the following description, and the detailed description thereof may be omitted.
[0030] As used herein, the terms comprising, including, and having specify the presence of features, integers, steps, operations, elements, components, or combinations thereof disclosed on the present disclosure, but do not preclude any one of features, integers, steps, operations, elements, components, and/or combinations thereof in advance.
[0031] Various examples of the present disclosure relate to a method for extracting aluminum. Various examples of the present disclosure relate to a method for extracting expensive pure aluminum from a low-priced aluminum alloy.
[0032]
[0033] Referring to
[0034] In the hydrogenation reaction step (S100), an aluminum alloy may react with sodium hydride (NaH). The aluminum alloy may be various aluminum alloys, such as cast aluminum, secondary aluminum, primary aluminum, and 3D printing aluminum powder. The aluminum alloy may be an alloy that further comprises a metallic element in addition to aluminum. For example, the aluminum alloy may mean an alloy that further comprises one or more of Si, Cu, Mg, Zn, Fe, Mn, Ni, Sn, or any combination thereof, in addition to aluminum.
[0035] The aluminum alloy may be in the form of a processed chip having a total length of 50 mm or less or a powder having a diameter of 5 mm or less.
[0036] In one example, NaH reacting with the aluminum alloy may be a single component. In one example, NaH may be a solid state.
[0037] The aluminum alloy and NaH may be prepared at a molar ratio of 1:1, for example.
[0038] In the hydrogenation reaction step (S100), hydrogen may be supplied. In the hydrogenation reaction step (S100), hydrogen may be supplied in a gaseous form. In the hydrogenation reaction step (S100), hydrogen may be supplied at a pressure of 80 bars to 90 bars. In the hydrogenation reaction step (S100), hydrogen may be supplied continuously.
[0039]
[0040] In the hydrogenation reaction step (S100), a reaction according to the following Reaction Formula may occur. In other words, in the hydrogenation reaction step (S100), NaAlH.sub.4 may be generated.
NaH(s)+aluminum alloy(s)+H.sub.2(g).fwdarw.NaAlH.sub.4(s)+Si(s), Mg(s), Cu(s), Fe(s), and the like.Reaction Formula
[0041] Next, the NaAlH.sub.4 separation step (S200) may be performed. In the NaAlH.sub.4 separation step (S200), NaAlH.sub.4 generated in the hydrogenation reaction step (S100) above may be separated.
[0042] In the NaAlH.sub.4 separation step (S200), NaAlH.sub.4 may be dissolved using a solvent. The solvent may be a solvent that dissolves NaAlH.sub.4. For example, the solvent may be one or more of tetrahydrofuran (THF), dioxane, acetone, dimethyl sulfoxide (DMSO), dimethylformamide (DMF), 1-methyl-2-pyrrolidone (NMP), or any combination thereof. In one example, the solvent may be tetrahydrofuran. For example, the solvent may comprise a single component of tetrahydrofuran.
[0043] The solvent may dissolve NaAlH.sub.4 and NaH in a solid state. The solvent may not react with trace metallic elements generated in the hydrogenation reaction step (S100). In other words, the solvent does not react with Si, Cu, Mg, Zn, Fe, Mn, Ni, Sn, and the like.
[0044] When the NaAlH.sub.4 is dissolved with the solvent, the dissolution may be performed at a temperature of less than 66 C. At a temperature of 66 C. or higher, the solvent may be evaporated. When the NaAlH.sub.4 is dissolved with the solvent, the dissolution may be maintained for at least 10 minutes.
[0045] In the NaAlH.sub.4 separation step (S200), a reaction according to the following Reaction Formula may occur.
NaAlH.sub.4(s)+solvent.fwdarw.NaAlH.sub.4(sol)Reaction Formula
[0046] Referring to
[0047] Next, the NaAlH.sub.4 solution dissolved in the solvent may be heated at a temperature of 66 C. or higher. Through this heating step, the solvent in the NaAlH.sub.4 solution may be evaporated. By evaporating the solvent, only the NaAlH.sub.4 may be separated. In one example, the evaporated solvent may be recaptured and recycled.
[0048] Next, in the dehydrogenation reaction step (S300), a reduction reaction of the separated NaAlH.sub.4(s) may occur. The dehydrogenation reaction step (S300) may be performed according to various examples. A first example and a second example is described below.
[0049]
[0050] In the heating of NaAlH.sub.4 (S311), the NaAlH.sub.4 separated in the NaAlH.sub.4 separation step (S200) may be heated at a first temperature. The first temperature may be 95 C. or higher. In one example, the first temperature may be 97.5 C. or higher. In another example, the first temperature may be 97.9 C. or higher. Through the heating of NaAlH.sub.4 (S311) at the first temperature, NaAlH.sub.4 may be decomposed into NaH, Al, and H.sub.2.
[0051] In the separating of the remaining NaAlH.sub.4 and NaH (S312), the unreacted NaAlH.sub.4 and NaH may be dissolved using a solvent. The solvent may be a solvent that dissolves only NaAlH.sub.4 and NaH in a solid state. For example, the solvent may be one or more of tetrahydrofuran (THF), dioxane, acetone, dimethyl sulfoxide (DMSO), dimethylformamide (DMF), 1-methyl-2-pyrrolidone (NMP), or any combination thereof. In one example, the solvent may be tetrahydrofuran. For example, the solvent may comprise a single component of tetrahydrofuran.
[0052] The separating of the remaining NaAlH.sub.4 and NaH (S312) may be performed at a temperature of less than 66 C. At a temperature of 66 C. or higher, the solvent may be evaporated. When the remaining NaAlH.sub.4 and NaH are dissolved in the solvent, the dissolution may be maintained for at least 10 minutes.
[0053] In the separating of the remaining NaAlH.sub.4 and NaH (S312), pure aluminum that is not dissolved in the solvent may be separated.
[0054] The dehydrogenation reaction step (S301) according to the first example may be performed by a ball milling process. The ball milling time may be within 5 hours. Through this, the carbon emissions may be reduced while maximally decomposing NaAlH.sub.4. For example, the remaining NaAlH.sub.4 that is not decomposed in the dehydrogenation reaction step (S301) according to the first example may be less than 10 wt % compared to initial NaAlH.sub.4.
[0055] The separating of the remaining NaAlH.sub.4 and NaH (S312) may further comprise recapturing NaH and H.sub.2. The recaptured NaH and H.sub.2 may be recycled and used in the hydrogenation reaction step (S100).
[0056] In the dehydrogenation reaction step (S301), a reaction according to the following Reaction Formula may occur. In the dehydrogenation reaction step (S301), a reduction reaction of NaAlH.sub.4(s) may occur.
NaAlH.sub.4(s).fwdarw.NaH(s)+Al(s)+2H.sub.2(g)Reaction Formula
[0057]
[0058] Referring to
[0059] Referring to
[0060] In the heating of NaAlH.sub.4 (S311), the NaAlH.sub.4 separated in the NaAlH.sub.4 separation step (S200) may be heated at a second temperature. The second temperature may be equal to or higher than a sodium (Na) evaporation temperature. For example, the second temperature may be 882 C. or higher. In the heating of NaAlH.sub.4 (S311), Na may be evaporated.
[0061] Referring to
Na(g)+H.sub.2(g).fwdarw.NaH(s)Reaction Formula
[0062] The NaH generated in the supplying of hydrogen (S312) may be accumulated on the cold upper plate (Cold). This NaH may be scraped off and reused.
[0063] Once the NaH generated in the supplying of hydrogen (S312) is removed, only pure aluminum may remain in the reactor. For example, pure aluminum may be accumulated on the hot lower plate (Hot) in the reactor.
[0064] Next, in the pure aluminum extraction step (S400), pure aluminum separated in the dehydrogenation reaction step (S300) may be extracted.
[0065] For example, in the separating of the remaining NaAlH.sub.4 and NaH (S312) of the dehydrogenation reaction step (S301) according to the first example, pure aluminum not dissolved in the solvent is separated through filter paper, and the corresponding aluminum may be extracted.
[0066] After removing the NaH generated in the supplying of hydrogen (S312) of the dehydrogenation reaction step (S302) according to the second example, pure aluminum may be extracted.
[0067] According to various examples of the present disclosure, the method of extracting aluminum may separate pure aluminum from an aluminum alloy containing a large amount of fine metallic elements. According to various examples of the present disclosure, the method of extracting aluminum may extract expensive pure aluminum from a low-priced aluminum alloy through a hydrogenation/dehydrogenation reaction of NaH.
[0068] According to various examples of the present disclosure, the method of extracting aluminum may recycle NaH, a solvent, hydrogen gas, and the like generated during an extraction process, so that the process is highly efficient and eco-friendly.
[0069] According to various examples of the present disclosure, the method of extracting aluminum may reduce CO.sub.2 emissions by about 84% or more compared to conventional aluminum extraction methods.
[0070] Hereinafter, the present disclosure is described in more detail by Examples. However, the following Examples and Experimental Examples are only intended to describe the present disclosure in more detail, and the scope of the present disclosure is not limited by the following Examples and Experimental Examples.
Example
[0071] Various aluminum alloys having compositions shown in Table 1 were prepared.
TABLE-US-00001 TABLE 1 Composition (wt. %) Ex. Cu Si Mg Zn Fe Mn Ni Sn Etc. Al Ex. 1 1.5~3.5 9.6~12.0 0.3 max. 1.0 max. 1.3 max. 0.5 max. 0.5 max. 0.3 max. 0.5 max. Rem. Ex. 2 0.35 max. 0.2~0.6 0.45~0.9 0.1 max. <0.1 Rem. Ex. 3 0.05 max. 9.0~10.0 0.25~0.45 0.1 max. 0.55 max 0.45 max. 0.05 max. 0.05 amx. Rem.
[0072] Example 1 was ADCl2 (secondary aluminum). Example 2 was A6005 (primary aluminum). Example 3 was 3D printing powder. The aluminum alloys of Examples 1-3 were prepared in the form of processed chips with a total length of 50 mm or less or in the form of powders with a diameter of 5 mm or less.
[0073] The aluminum alloys of Examples 1-3 and NaH were charged into a ball milling device, and hydrogen gas was supplied at 83 Bar to induce a hydrogenation reaction.
[0074] As a result of the hydrogenation reaction, NaAlH.sub.4(s) was generated. Since the aluminum alloy that participated in the reaction contained trace elements such as Si, Mg, Cu, and Fe in addition to aluminum, the corresponding trace elements were included after the hydrogenation reaction.
[0075] Next, NaAlH.sub.4 was dissolved using tetrahydrofuran (THF) as a solvent. The NaAlH.sub.4 solution passed through a filter. Since the solvent did not react with trace elements such as Si, Mg, Cu, and Fe, the corresponding trace elements were separated by a filter. The NaAlH.sub.4 solution was heated at a temperature of 66 C. or higher to evaporate and recapture THF. Thereafter, solid NaAlH.sub.4 remained.
[0076] Next, the solid NaAlH.sub.4 was charged into the ball milling device again and applied with a temperature of 97.9 C. or higher. NaAlH.sub.4 was decomposed into NaH(s), Al(s), and H.sub.2(g). After the reaction was completed, H.sub.2(g) was captured as gas, and solid pure aluminum, NaH(s), and unreacted NaAlH.sub.4(s) remained. The remaining NaAlH.sub.4(s) and NaH(s) were dissolved in THF, and pure aluminum was separated using filter paper. The NaH(s) and H.sub.2(g) were recaptured and recycled.
Experimental Example 1: Comparison of Carbon Dioxide Emissions
[0077] The carbon dioxide emissions of a conventional aluminum extraction method and an aluminum extraction method using ADCl2 (secondary aluminum) of Example 1 were compared. Specifically, according to the conventional aluminum extraction method, a graphite anode, a graphite cathode, and molten cryolite as an electrolyte were prepared in a steel tank and then electrolyzed.
[0078] A carbon oxidation reaction occurred at the anode as follows:
##STR00001##
[0079] A carbon reduction reaction occurred at the cathode as follows:
##STR00002##
[0080] The overall Reaction Formula was as follows:
##STR00003##
[0081] Molten aluminum was extracted through this reaction. The CO.sub.2 emissions when extracting 1 kg of aluminum were 16 kg.
[0082] On the other hand, when the aluminum extraction method using ADC12 (secondary aluminum) of Example 1 was used, the CO.sub.2 emissions when extracting 1 kg of aluminum were 2.5 kg.
[0083] In other words, it was confirmed that aluminum extraction methods of the Examples above could reduce the CO.sub.2 emissions by about 84% compared to the conventional aluminum extraction method.
[0084] Hereinabove, the examples of the present disclosure have been described together with the drawings. The examples are illustrative, and the present disclosure is not limited to the above-described examples and the contents of the drawings.
[0085] It should be apparent to those having ordinary skill in the art that modifications of the present disclosure may be made within the scope of the disclosed technical idea. The described examples should be considered as part of the present disclosure, and the scope of the present disclosure should not be limited only to the described examples.
[0086] The scope of the present disclosure should be judged by the technical ideas set forth in the appended claims. In addition, even if the actions or effects according to the configuration are not explicitly described while explaining the embodiments of the present disclosure, it is understood that the actions or effects that may be predicted by the configuration should also be recognized as the present disclosure.