EP0375308A1 - Process and apparatus for producing high purity aluminum - Google Patents
Process and apparatus for producing high purity aluminum Download PDFInfo
- Publication number
- EP0375308A1 EP0375308A1 EP89313184A EP89313184A EP0375308A1 EP 0375308 A1 EP0375308 A1 EP 0375308A1 EP 89313184 A EP89313184 A EP 89313184A EP 89313184 A EP89313184 A EP 89313184A EP 0375308 A1 EP0375308 A1 EP 0375308A1
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- European Patent Office
- Prior art keywords
- vessel
- aluminum
- impeller
- crystallizer
- molten aluminum
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 59
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 59
- 238000000034 method Methods 0.000 title claims abstract description 32
- 238000001816 cooling Methods 0.000 claims abstract description 34
- 239000012809 cooling fluid Substances 0.000 claims abstract description 11
- 238000003756 stirring Methods 0.000 claims abstract description 11
- 238000002844 melting Methods 0.000 claims abstract description 10
- 230000008018 melting Effects 0.000 claims abstract description 10
- 239000012535 impurity Substances 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 7
- 229910052796 boron Inorganic materials 0.000 claims description 7
- 238000002425 crystallisation Methods 0.000 claims description 5
- 230000008025 crystallization Effects 0.000 claims description 5
- 239000003595 mist Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 238000001640 fractional crystallisation Methods 0.000 abstract description 7
- 239000007787 solid Substances 0.000 description 16
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 239000000155 melt Substances 0.000 description 11
- 238000013019 agitation Methods 0.000 description 9
- 239000002826 coolant Substances 0.000 description 9
- 239000013078 crystal Substances 0.000 description 9
- 238000007711 solidification Methods 0.000 description 7
- 230000008023 solidification Effects 0.000 description 7
- 230000005496 eutectics Effects 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 238000007670 refining Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 210000001787 dendrite Anatomy 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 229910001338 liquidmetal Inorganic materials 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- FGUJWQZQKHUJMW-UHFFFAOYSA-N [AlH3].[B] Chemical compound [AlH3].[B] FGUJWQZQKHUJMW-UHFFFAOYSA-N 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000011031 large-scale manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D9/00—Cooling of furnaces or of charges therein
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B21/00—Obtaining aluminium
- C22B21/06—Obtaining aluminium refining
Definitions
- This invention relates to a process and apparatus for producing high purity aluminum, particularly by fractional crystallization.
- High purity aluminum is widely used to produce automotive and other bright surface products.
- a highly desirable aluminum having excellent brightness is one of 99.95% ⁇ 0.02 purity containing less than 0.05 wt% iron and silicon.
- This high purity aluminum is typically produced by one or a combination of the following techniques: zone refining, three layer refining and fractional crystallization.
- the zone refining and three layer refining both require high investment, expensive maintenance and very skilled personnel.
- fractional crystallization tends to be easier to operate, requires minimal investment and is cheaper to run.
- the principal objective of fractional crystallization is to form a purified solid phase from an impure liquid phase.
- a body of molten aluminum containing eutectic impurities, i.e. Fe, Si, Cu, etc. which undergo a eutectic reaction with aluminum is subjected to cooling, the crystals which solidify are richer in aluminum content than the liquid body from which they came. It is, therefore, possible by partial solidification of the melt to produce a solid fraction with higher purity than the original melt.
- Mitsubishi, Japanese Patent 1984-28538 describes a system in which molten aluminum is accommodated in a vessel with a horizontal floor. The metal is purified by the extraction of heat through the cooled floor while liquid aluminum is stirred. Cracking problems in the floor and expansion problems with cooling pipes created serious operational difficulties for the Mitsubishi method.
- the process of this invention for producing high purity aluminum comprises the steps of melting aluminum containing eutectic impurities to obtain a body of molten aluminum, holding the molten aluminum within a vertical, cylindrical crystallizer vessel, passing cooling fluid through a cooling jacket at least partially surrounding the vessel walls and stirring the molten aluminum within the vessel whereby high purity aluminum crystallizes on the cooled inner surface of the cylindrical vessel.
- the molten aluminum is preferably provided in the crystallizer vessel by mounting the crystallizer on top of a melting furnace, e.g. an electromagnetic furnace.
- the aluminum to be purified is added and melted until the height of the molten aluminum reaches the level of the top of the cooling jacket.
- the aluminum may also contain peritectic impurities, such as vanadium and titanium. If so, an optional prior treatment with boron may be carried out by known methods to remove such impurities.
- the methods include the following:
- molten metal temperature, molten metal agitation and the cooling method all affect the quality of the final product. It is found advantageous to use an air/water mist flow for cooling and it has been found that the level of impurities in the purified solid decreases with increased speed of agitation and decreased coolant flow, i.e. lower solidification rate.
- This coolant flow is obtained by varying the water to air ratio in the coolant mix, either by decreasing the water flow or increasing the air flow.
- the eutectic impurities are rejected from the solid into the liquid phase to form a boundary layer of concentrated impurities in the vicinity of the liquid-solid interface.
- the impurity content in the boundary layer increases, the solid/liquid interface changes from a smooth regular crystal front to a dendritic structure.
- the thick thermal boundary layer in inefficiently mixed vessels also encourages the growth of dendrites.
- the dendrites that form at the interface have a tendency to entrap the mother liquid enriched with impurities in their interstices. Therefore their formation is undesirable.
- strong agitation of the melt is desirable.
- agitation of the melt increases the rate of mass transfer because the impurities are more rapidly transferred from the solid/liquid interface to the melt.
- an impeller speed in the order of about 150 to 250 rpm is preferred.
- the cooling rate must also be carefully controlled. In order to minimize occlusion of impurities in the crystalline solid, it is desirable to form perfect crystals. However, the more perfect crystal growth occurs at low rates of crystallization. Moreover, as the rate of crystallization is decreased, the rate of buildup of impurities at the solid/liquid interface is reduced. This results in greater separation since decreasing the cooling flow rate decreases the rate of solidification. Of course, there is a lower limit on the level of cooling flow rate and it is must be sufficiently high to produce a rate of heat transfer sufficient to provide the degree of supersaturation necessary for crystallization.
- the invention also relates to an apparatus for producing high-purity aluminum comprising (a) a vertical, cylindrical crystallizer vessel at least partially surrounded by a cooling jacket for passage of cooling fluid therethrough and having an open bottom end, (b) a melting furnace connected below the open bottom end of the crystallizer vessel, said furnace being adapted to melt aluminum and provide molten aluminum within the crystallizer vessel and (c) an elongated impeller axially rotatably mounted within the crystallizer vessel, said impeller being adapted to stir the molten aluminum in the crystallizer vessel while passing cooling fluid through the cooling jacket thereby crystallizing high purity aluminum on the cooled inner vessel wall.
- the drawing is a view in vertical section showing one preferred embodiment of an apparatus for producing high purity aluminum by the process of the invention.
- the apparatus consists of a cylindrically shaped crystallizer vessel 10 with an open bottom resting on top of an electromagnetic furnace 11.
- the vessel 10 rests on a support 14 on top of furnace 11 which is mounted in a cabinet assembly 15.
- the crystallizer vessel and furnace are both manufactured with silicon carbide refractory walls and the crystallizer vessel 10 has a cylindrical inner chamber 12.
- a cooling jacket 13 in the form of a hollow wall portion surrounds the vessel 10 and is connected to inlet lines (not shown) for air and water.
- a graphite impeller 17 with radial vanes Mounted axially within chamber 12 is a graphite impeller 17 with radial vanes.
- the impeller is driven by a drive shaft 22 extending through removable insulated top 23 and connecting to a motor assembly 18 mounted on top of vessel 10.
- Insulation is also provided between the vessel 10 and the electromagnetic furnace 12 and further portions of insulation 19 are provided adjacent portions of the cooling jacket.
- part of the aluminum to be purified is placed within cavity 20 of furnace 11 to be melted and the rest of the aluminum to be purified is added gradually until the height of the molten metal reaches the level of the top of the cooling jacket 13. While stirring the molten aluminum with the impeller 17, the molten metal is cooled by a mist flow of air and water passing through cooling jacket 13. This results in high purity aluminum 21 solidifying on the cooled wall of chamber 12.
- the stirring action disperses a layer of molten metal that stays close to the solidification boundary and is rich in impurities away from the boundary and into the molten metal mass. In this manner, the impurities are not pulled into the solids forming on the wall of the vessel and the purity of the final aluminum is improved.
- the stirring system 17, 18 and top 23 are removed and the liquid metal is poured out by tilting the crystallizer using a hydraulic mechanism, leaving an annular form 21 of purified solid which, after cooling, is removed from the vessel 10.
- the upper half of the crystallizer walls are designed so as to have a few degrees of taper to enable easy removal of the purified solid formed on the walls. Contraction during cooling makes subsequent removal easy. No cutting is necessary.
- the above reactor was used to conduct various experiments on an impure aluminum alloy containing 99.7% by weight aluminum.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
A process and apparatus are described for producing high purity aluminum by fractional crystallization. This process comprises the steps of melting the aluminum to be purified to obtain a molten aluminum, holding the molten aluminum within a vertical, cylindrical crystallizer vessel at least partially surrounded by a cooling jacket for the passage of cooling fluid therethrough, and stirring the molten aluminum in the vessel while passing cooling fluid through the cooling jacket thereby crystallizing high purity aluminum on the cooled inner vessel wall. An apparatus for carrying out the above process is also described.
Description
- This invention relates to a process and apparatus for producing high purity aluminum, particularly by fractional crystallization.
- High purity aluminum is widely used to produce automotive and other bright surface products. For instance, a highly desirable aluminum having excellent brightness is one of 99.95% ± 0.02 purity containing less than 0.05 wt% iron and silicon. This high purity aluminum is typically produced by one or a combination of the following techniques: zone refining, three layer refining and fractional crystallization. The zone refining and three layer refining both require high investment, expensive maintenance and very skilled personnel. On the other hand, fractional crystallization tends to be easier to operate, requires minimal investment and is cheaper to run.
- The principal objective of fractional crystallization is to form a purified solid phase from an impure liquid phase. When a body of molten aluminum containing eutectic impurities, i.e. Fe, Si, Cu, etc. which undergo a eutectic reaction with aluminum, is subjected to cooling, the crystals which solidify are richer in aluminum content than the liquid body from which they came. It is, therefore, possible by partial solidification of the melt to produce a solid fraction with higher purity than the original melt.
- Among specific prior systems for producing high purity aluminum, there may be mentioned that described in Alcoa, U.S. Patent 3,211,547. In the Alcoa method, crystals are formed on the free surface of a molten metal bath and these are allowed to fall to the bottom by gravity to form aggregates of crystals by pressing, thereby separating the crystals from the molten metal. This method suffers from the entrapment of impurities between the crystals collected at the bottom. Further deficiencies are a large diffusion layer between the interface and the liquid and a small temperature gradient.
- Reynolds, U.S. Patent 3,163,895 describes a process comprising continuous fractional crystallization of a liquid aluminum feed stream under strong agitation at the solid/liquid interface. The process needs high investment costs and maintenance is difficult and costly.
- In Pechiney, U.S. Patent 3,671,229 there is described a system generally similar to that of the Alcoa method, but it is generally not suitable for large scale production and long treatment times are required for small quantities of high purity aluminum.
- Mitsubishi, Japanese Patent 1984-28538 describes a system in which molten aluminum is accommodated in a vessel with a horizontal floor. The metal is purified by the extraction of heat through the cooled floor while liquid aluminum is stirred. Cracking problems in the floor and expansion problems with cooling pipes created serious operational difficulties for the Mitsubishi method.
- Showa, U.S. Patent 4,469,512 describes a purification method by adding boron to molten aluminum and rotating a cooling body immersed in the boron-containing molten aluminum while introducing a cooling fluid to the interior of the cooling body. This provides a small area of crystallization. Therefore, to increase the surface area, additional vessels identical to each other are set up in series, increasing both the cost and difficulty of the process.
- It is the object of the present invention to provide a simpler and less expensive technique for fractional crystallization than has been possible by other methods.
- The process of this invention for producing high purity aluminum comprises the steps of melting aluminum containing eutectic impurities to obtain a body of molten aluminum, holding the molten aluminum within a vertical, cylindrical crystallizer vessel, passing cooling fluid through a cooling jacket at least partially surrounding the vessel walls and stirring the molten aluminum within the vessel whereby high purity aluminum crystallizes on the cooled inner surface of the cylindrical vessel.
- The molten aluminum is preferably provided in the crystallizer vessel by mounting the crystallizer on top of a melting furnace, e.g. an electromagnetic furnace. The aluminum to be purified is added and melted until the height of the molten aluminum reaches the level of the top of the cooling jacket.
- In this manner, eutectic impurities are removed and an annular body of solid, high purity aluminum is formed. The stirring action disperses a layer of molten metal that stays close to the solidification boundary and tends to urge the impurities away from the boundary and into the molten metal. Thus, the impurities do not tend to be trapped in the solids and the purity of the solid product is improved. When the process is completed, the stirring system is removed, the remaining liquid metal is poured out and the purified solid product is cooled and removed from the reactor.
- The aluminum may also contain peritectic impurities, such as vanadium and titanium. If so, an optional prior treatment with boron may be carried out by known methods to remove such impurities.
- The methods include the following:
- 1. Addition of boron as potassium borofluoride;
- 2. Addition of boron as an aluminium-boron master alloy;
- 3. Addition of boron by the method disclosed in co-assigned Canadian patent No. 1,215,236.
- With the system of the present invention, molten metal temperature, molten metal agitation and the cooling method all affect the quality of the final product. It is found advantageous to use an air/water mist flow for cooling and it has been found that the level of impurities in the purified solid decreases with increased speed of agitation and decreased coolant flow, i.e. lower solidification rate. This coolant flow is obtained by varying the water to air ratio in the coolant mix, either by decreasing the water flow or increasing the air flow.
- Best results appear to be obtained with a melt temperature in the order of 660°C ± 0.5°C. Of course, in terms of temperatures, it is a matter of the relationship between the cooling rate and the melt temperature such that the desired freezing rate at the solid/liquid interface is achieved.
- During crystal growth, the eutectic impurities are rejected from the solid into the liquid phase to form a boundary layer of concentrated impurities in the vicinity of the liquid-solid interface. As the impurity content in the boundary layer increases, the solid/liquid interface changes from a smooth regular crystal front to a dendritic structure. The thick thermal boundary layer in inefficiently mixed vessels also encourages the growth of dendrites. The dendrites that form at the interface have a tendency to entrap the mother liquid enriched with impurities in their interstices. Therefore their formation is undesirable. To remove this entrapped mother liquid and to reduce the thickness of the thermal boundary layer, strong agitation of the melt is desirable. Thus, agitation of the melt increases the rate of mass transfer because the impurities are more rapidly transferred from the solid/liquid interface to the melt. The higher the rate of agitation, the better is the mass transfer of impurities. Typically, an impeller speed in the order of about 150 to 250 rpm is preferred.
- The cooling rate must also be carefully controlled. In order to minimize occlusion of impurities in the crystalline solid, it is desirable to form perfect crystals. However, the more perfect crystal growth occurs at low rates of crystallization. Moreover, as the rate of crystallization is decreased, the rate of buildup of impurities at the solid/liquid interface is reduced. This results in greater separation since decreasing the cooling flow rate decreases the rate of solidification. Of course, there is a lower limit on the level of cooling flow rate and it is must be sufficiently high to produce a rate of heat transfer sufficient to provide the degree of supersaturation necessary for crystallization.
- It has been found that a particularly satisfactory result is obtained using as a coolant a mixture of air and water in which a small amount of water is added to an air flow before entering the cooling jacket. This creates a mist flow of very fine droplets of water.
- The invention also relates to an apparatus for producing high-purity aluminum comprising (a) a vertical, cylindrical crystallizer vessel at least partially surrounded by a cooling jacket for passage of cooling fluid therethrough and having an open bottom end, (b) a melting furnace connected below the open bottom end of the crystallizer vessel, said furnace being adapted to melt aluminum and provide molten aluminum within the crystallizer vessel and (c) an elongated impeller axially rotatably mounted within the crystallizer vessel, said impeller being adapted to stir the molten aluminum in the crystallizer vessel while passing cooling fluid through the cooling jacket thereby crystallizing high purity aluminum on the cooled inner vessel wall.
- The invention will be described below in greater detail with reference to the accompanying drawing.
- The drawing is a view in vertical section showing one preferred embodiment of an apparatus for producing high purity aluminum by the process of the invention.
- The apparatus consists of a cylindrically shaped
crystallizer vessel 10 with an open bottom resting on top of anelectromagnetic furnace 11. Thevessel 10 rests on asupport 14 on top offurnace 11 which is mounted in acabinet assembly 15. The crystallizer vessel and furnace are both manufactured with silicon carbide refractory walls and thecrystallizer vessel 10 has a cylindricalinner chamber 12. A coolingjacket 13 in the form of a hollow wall portion surrounds thevessel 10 and is connected to inlet lines (not shown) for air and water. - Mounted axially within
chamber 12 is agraphite impeller 17 with radial vanes. The impeller is driven by adrive shaft 22 extending through removable insulated top 23 and connecting to amotor assembly 18 mounted on top ofvessel 10. - Insulation is also provided between the
vessel 10 and theelectromagnetic furnace 12 and further portions ofinsulation 19 are provided adjacent portions of the cooling jacket. - In operation, part of the aluminum to be purified is placed within
cavity 20 offurnace 11 to be melted and the rest of the aluminum to be purified is added gradually until the height of the molten metal reaches the level of the top of the coolingjacket 13. While stirring the molten aluminum with theimpeller 17, the molten metal is cooled by a mist flow of air and water passing through coolingjacket 13. This results inhigh purity aluminum 21 solidifying on the cooled wall ofchamber 12. - The stirring action disperses a layer of molten metal that stays close to the solidification boundary and is rich in impurities away from the boundary and into the molten metal mass. In this manner, the impurities are not pulled into the solids forming on the wall of the vessel and the purity of the final aluminum is improved. When the process has been completed, the stirring
system annular form 21 of purified solid which, after cooling, is removed from thevessel 10. The upper half of the crystallizer walls are designed so as to have a few degrees of taper to enable easy removal of the purified solid formed on the walls. Contraction during cooling makes subsequent removal easy. No cutting is necessary. - The reactor described above had the following characteristics:
- Crystallizer capacity: 200 kg
- Melting furnace capacity: 200 kg
- Power capacity during melting: 80 kw
- Power capacity to keep the charge at constant temperature: 10 kw
- Inside area of the reactor: 6900 cm2 (1070 in2)
- Height of reactor: 76 cm (30 in.)
- Inside diameter: 43 cm (17 in.)
- Height of cooling jacket: 51 cm (20 in.)
- Width of cooling jacket: 1 cm (3/8 in.)
- Maximum flow of cooling air: 7080 liters/minute (250 SCFM)
- Maximum flow of cooling water: 1.0 kg/minute
- The above reactor was used to conduct various experiments on an impure aluminum alloy containing 99.7% by weight aluminum.
- (A) In order to study the effects of temperature, tests were conducted at 670°C and 665°C, but very little solidification occurred at these temperatures. To be effective at these temperatures, a greater cooling rate would have been necessary from the cooling jacket. Good solid growth was obtained when the molten metal was kept at 660°C. At this temperature, it was found to be easy to adjust the power of the furnace to keep the molten charge at constant temperature. This consumed about 10 kw of power.
- For these tests an air flow of 4250 liters/minute was used together with a water flow of 0.40 kg/minute and a melt temperature of 660°C. The rate of agitation was varied and it was found that agitation at speeds below 150 rpm was insufficient for mixing of the melt, while a speed in excess of 250 rpm tended to splash the melt on top of the inside wall of the reactor and cause freezing. The results obtained are shown in Table 1 below:
-
- The effect of decreasing the ratio of water coolant per unit volume of air coolant (col. 2) is to decrease the solidification rate. This tended to improve purification.
-
- The results show that increasing the water coolant flow rate and hence the ratio of water coolant to air coolant (col. 2) increases the rate of heat transfer and tends to decrease the purification of eutectic elements (Fe + Si).
-
- The preferred practice of our invention has by example and otherwise been explained in detail but we do not desire to be limited to such specific description except as expressed in the appended claims.
Claims (15)
1. A process for producing high-purity aluminum comprising the steps of melting the aluminum to be purified to obtain a molten aluminum, holding the molten aluminum within a vertical, cylindrical crystallizer vessel at least partially surrounded by a cooling jacket for the passage of cooling fluid therethrough, and stirring the molten aluminum in the vessel while passing cooling fluid through the cooling jacket thereby crystallizing high purity aluminum on the cooled inner vessel wall.
2. A process according to claim 1 wherein the crystallizer vessel is positioned on top of a melting furnace which provides the molten aluminum for the crystallizer vessel.
3. A process according to claim 2 wherein the stirring is conducted by means of a rotating elongated impeller mounted axially within the cylindrical crystallizer vessel.
4. A process according to claim 3 wherein the impeller is rotated at a rate of about 150 to 250 rpm.
5. A process according to claim 2 wherein peritectic impurities are removed from the molten aluminum by treatment with boron prior to crystallization.
6. A process according to claim 2 wherein the cooling fluid is an air/water mixture.
7. A process according to claim 6 wherein the air/water mixture is a mist flow of very fine droplets of water.
8. A process according to claim 3 wherein upon completion of the process, the impeller is removed from the vessel and an annulus of purified aluminum is removed from the vessel.
9. An apparatus for producing high-purity aluminum comprising (a) a vertical, cylindrical crystallizer vessel at least partially surrounded by a cooling jacket for passage of cooling fluid therethrough and having an open bottom end, (b) a melting furnace connected below the open bottom end of the crystallizer vessel, said furnace being adapted to melt aluminum and provide molten aluminum within the crystallizer vessel and (c) an elongated impeller axially rotatably mounted within the crystallizer vessel, said impeller being adapted to stir the molten aluminum in the crystallizer vessel while passing cooling fluid through the cooling jacket thereby crystallizing high purity aluminum on the cooled inner vessel wall.
10. An apparatus according to claim 9 wherein the impeller has radially extending vanes.
11. An apparatus according to claim 9 wherein the crystallizer vessel has an insulated top with a drive shaft for the impeller extending through said top.
12. An apparatus according to claim 11 wherein a drive motor for the impeller is mounted outside the crystallizer vessel.
13. An apparatus according to claim 9 wherein the cooling jacket comprises a hollow wall portion.
14. An apparatus according to claim 13 wherein the melting furnace is a cylindrical vessel surrounded by an electromagnetic heater.
15. An apparatus according to claim 11 wherin the top and impeller are removable to permit removal of an annulus of purified aluminum from the vessel.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA586886 | 1988-12-22 | ||
CA586886 | 1988-12-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0375308A1 true EP0375308A1 (en) | 1990-06-27 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89313184A Withdrawn EP0375308A1 (en) | 1988-12-22 | 1989-12-18 | Process and apparatus for producing high purity aluminum |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0375308A1 (en) |
JP (1) | JPH02225633A (en) |
KR (1) | KR900010026A (en) |
AU (1) | AU4703289A (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5110352A (en) * | 1990-05-28 | 1992-05-05 | Showa Aluminum Corporation | Method of producing aluminum material for use as electronic material |
EP1288319A1 (en) * | 2001-09-03 | 2003-03-05 | Corus Technology BV | Method for the purification of an aluminium alloy |
EP1380658A1 (en) * | 2002-07-05 | 2004-01-14 | Corus Technology BV | Method for fractional crystallisation of a molten metal |
NL1023009C2 (en) * | 2003-03-25 | 2004-09-30 | Univ Delft Tech | Method for recovering a metal from a mixture. |
WO2005049875A1 (en) * | 2003-11-19 | 2005-06-02 | Corus Technology Bv | Method of cooling molten metal during fractional crystallisation |
US7442228B2 (en) | 2001-10-03 | 2008-10-28 | Aleris Switzerland Gmbh C/O K+P Treuhangesellschaft | Method and device for controlling the proportion of crystals in a liquid-crystal mixture |
US7531023B2 (en) | 2004-03-19 | 2009-05-12 | Aleris Switzerland Gmbh | Method for the purification of a molten metal |
US7648559B2 (en) | 2002-07-05 | 2010-01-19 | Aleris Switzerland Gmbh C/O K+P Treuhangesellschaft | Method for fractional crystallisation of a metal |
US7892318B2 (en) | 2006-06-28 | 2011-02-22 | Aleris Switzerland Gmbh C/O K+P Treuhandgesellschaft | Crystallisation method for the purification of a molten metal, in particular recycled aluminium |
US7955414B2 (en) | 2006-07-07 | 2011-06-07 | Aleris Switzerland Gmbh | Method and device for metal purification and separation of purified metal from metal mother liquid such as aluminium |
CN102534246A (en) * | 2011-12-27 | 2012-07-04 | 昆明冶金研究院 | Preparation method of high-purity aluminum |
US8313554B2 (en) | 2006-06-22 | 2012-11-20 | Aleris Switzerland Gmbh | Method for the separation of molten aluminium and solid inclusions |
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CN113652553A (en) * | 2021-08-19 | 2021-11-16 | 武汉拓材科技有限公司 | Production device and method of high-purity gallium |
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CN118500126A (en) * | 2024-07-09 | 2024-08-16 | 安徽朗盛环能科技有限公司 | Nickel plate purification decarburization deoxidization equipment and process |
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CN111575501A (en) * | 2020-06-24 | 2020-08-25 | 江苏金海铝业有限公司 | Method for extracting ultra-high purity aluminum by directional solidification under electromagnetic stirring |
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Cited By (25)
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US5110352A (en) * | 1990-05-28 | 1992-05-05 | Showa Aluminum Corporation | Method of producing aluminum material for use as electronic material |
EP1288319A1 (en) * | 2001-09-03 | 2003-03-05 | Corus Technology BV | Method for the purification of an aluminium alloy |
WO2003020991A1 (en) * | 2001-09-03 | 2003-03-13 | Corus Technology Bv | Method for the purification of an aluminium alloy |
US7442228B2 (en) | 2001-10-03 | 2008-10-28 | Aleris Switzerland Gmbh C/O K+P Treuhangesellschaft | Method and device for controlling the proportion of crystals in a liquid-crystal mixture |
EP1380658A1 (en) * | 2002-07-05 | 2004-01-14 | Corus Technology BV | Method for fractional crystallisation of a molten metal |
WO2004005558A1 (en) * | 2002-07-05 | 2004-01-15 | Corus Technology Bv | Method for fractional crystallisation of a molten metal |
US7648559B2 (en) | 2002-07-05 | 2010-01-19 | Aleris Switzerland Gmbh C/O K+P Treuhangesellschaft | Method for fractional crystallisation of a metal |
US7419530B2 (en) | 2002-07-05 | 2008-09-02 | Aleris Switzerland Gmbh C/O K+P Treuhangesellschaft | Method for fractional crystallisation of a molten metal |
NL1023009C2 (en) * | 2003-03-25 | 2004-09-30 | Univ Delft Tech | Method for recovering a metal from a mixture. |
WO2004085686A2 (en) * | 2003-03-25 | 2004-10-07 | Technische Universiteit Delft | Method of recovering a metal from a mixture by melt freeze fractionation |
WO2004085686A3 (en) * | 2003-03-25 | 2004-12-02 | Univ Delft Tech | Method of recovering a metal from a mixture by melt freeze fractionation |
US7537639B2 (en) | 2003-11-19 | 2009-05-26 | Aleris Switzerland Gmbh | Method of cooling molten metal during fractional crystallisation |
CN100513601C (en) * | 2003-11-19 | 2009-07-15 | 阿勒里斯瑞士有限公司 | Method of cooling molten metal during fractional crystallisation |
WO2005049875A1 (en) * | 2003-11-19 | 2005-06-02 | Corus Technology Bv | Method of cooling molten metal during fractional crystallisation |
US7531023B2 (en) | 2004-03-19 | 2009-05-12 | Aleris Switzerland Gmbh | Method for the purification of a molten metal |
US8313554B2 (en) | 2006-06-22 | 2012-11-20 | Aleris Switzerland Gmbh | Method for the separation of molten aluminium and solid inclusions |
US7892318B2 (en) | 2006-06-28 | 2011-02-22 | Aleris Switzerland Gmbh C/O K+P Treuhandgesellschaft | Crystallisation method for the purification of a molten metal, in particular recycled aluminium |
US7955414B2 (en) | 2006-07-07 | 2011-06-07 | Aleris Switzerland Gmbh | Method and device for metal purification and separation of purified metal from metal mother liquid such as aluminium |
CN102534246A (en) * | 2011-12-27 | 2012-07-04 | 昆明冶金研究院 | Preparation method of high-purity aluminum |
WO2021071381A1 (en) * | 2019-10-11 | 2021-04-15 | Юрий Иванович ОСИПОВ | Method for purifying aluminium and its alloys |
RU2731948C1 (en) * | 2019-10-16 | 2020-09-09 | Юрий Иванович Осипов | Method of cleaning aluminum and its alloys from intermetallides and other non-metallic inclusions |
CN113652553A (en) * | 2021-08-19 | 2021-11-16 | 武汉拓材科技有限公司 | Production device and method of high-purity gallium |
CN115747515A (en) * | 2022-11-25 | 2023-03-07 | 宁波锦越新材料有限公司 | A high-purity aluminum continuous purification equipment |
CN115747515B (en) * | 2022-11-25 | 2023-07-14 | 宁波锦越新材料有限公司 | A high-purity aluminum continuous purification equipment |
CN118500126A (en) * | 2024-07-09 | 2024-08-16 | 安徽朗盛环能科技有限公司 | Nickel plate purification decarburization deoxidization equipment and process |
Also Published As
Publication number | Publication date |
---|---|
AU4703289A (en) | 1990-06-28 |
JPH02225633A (en) | 1990-09-07 |
KR900010026A (en) | 1990-07-06 |
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