US3743263A - Apparatus for refining molten aluminum - Google Patents
Apparatus for refining molten aluminum Download PDFInfo
- Publication number
- US3743263A US3743263A US00211950A US3743263DA US3743263A US 3743263 A US3743263 A US 3743263A US 00211950 A US00211950 A US 00211950A US 3743263D A US3743263D A US 3743263DA US 3743263 A US3743263 A US 3743263A
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- gas
- metal
- vessel
- refining
- molten metal
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- 238000007670 refining Methods 0.000 title claims abstract description 69
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 41
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 39
- 229910052751 metal Inorganic materials 0.000 claims abstract description 137
- 239000002184 metal Substances 0.000 claims abstract description 137
- 238000002347 injection Methods 0.000 claims abstract description 31
- 239000007924 injection Substances 0.000 claims abstract description 31
- 239000000155 melt Substances 0.000 claims abstract description 31
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 238000007599 discharging Methods 0.000 claims description 8
- 229910002804 graphite Inorganic materials 0.000 claims description 8
- 239000010439 graphite Substances 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 7
- 238000001802 infusion Methods 0.000 claims description 4
- 238000005553 drilling Methods 0.000 claims description 3
- 239000007789 gas Substances 0.000 abstract description 140
- 239000011261 inert gas Substances 0.000 abstract description 36
- 238000000034 method Methods 0.000 abstract description 13
- 230000008569 process Effects 0.000 abstract description 7
- 239000000460 chlorine Substances 0.000 description 27
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 25
- 229910052801 chlorine Inorganic materials 0.000 description 25
- 229910045601 alloy Inorganic materials 0.000 description 24
- 239000000956 alloy Substances 0.000 description 24
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 21
- 239000001257 hydrogen Substances 0.000 description 21
- 229910052739 hydrogen Inorganic materials 0.000 description 21
- 239000012535 impurity Substances 0.000 description 17
- 238000005266 casting Methods 0.000 description 13
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 229910000838 Al alloy Inorganic materials 0.000 description 9
- 239000002245 particle Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 229940063656 aluminum chloride Drugs 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000004907 flux Effects 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000003517 fume Substances 0.000 description 3
- 229910001629 magnesium chloride Inorganic materials 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000002035 prolonged effect Effects 0.000 description 3
- 239000011819 refractory material Substances 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 238000010924 continuous production Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000013528 metallic particle Substances 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000000809 air pollutant Substances 0.000 description 1
- 231100001243 air pollutant Toxicity 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 229940000425 combination drug Drugs 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000009658 destructive testing Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 238000005242 forging Methods 0.000 description 1
- 150000004820 halides Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052743 krypton Inorganic materials 0.000 description 1
- DNNSSWSSYDEUBZ-UHFFFAOYSA-N krypton atom Chemical compound [Kr] DNNSSWSSYDEUBZ-UHFFFAOYSA-N 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- 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
- C22B9/00—General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/20—Mixing gases with liquids
- B01F23/23—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids
- B01F23/233—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements
- B01F23/2331—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements characterised by the introduction of the gas along the axis of the stirrer or along the stirrer elements
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/20—Mixing gases with liquids
- B01F23/23—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids
- B01F23/233—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements
- B01F23/2331—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements characterised by the introduction of the gas along the axis of the stirrer or along the stirrer elements
- B01F23/23311—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements characterised by the introduction of the gas along the axis of the stirrer or along the stirrer elements through a hollow stirrer axis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/20—Mixing gases with liquids
- B01F23/23—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids
- B01F23/2366—Parts; Accessories
- B01F23/2368—Mixing receptacles, e.g. tanks, vessels or reactors, being completely closed, e.g. hermetically closed
-
- 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
- C22B21/066—Treatment of circulating aluminium, e.g. by filtration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/20—Mixing gases with liquids
- B01F23/23—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids
- B01F23/233—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements
- B01F23/2331—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements characterised by the introduction of the gas along the axis of the stirrer or along the stirrer elements
- B01F23/23314—Mixing gases with liquids by introducing gases into liquid media, e.g. for producing aerated liquids using driven stirrers with completely immersed stirring elements characterised by the introduction of the gas along the axis of the stirrer or along the stirrer elements through a hollow stirrer element
Definitions
- the apparatus of the invention is capable of injecting gas in the form of small discrete bubbles into a mass of molten metal.
- the apparatus comprises a rotatable shaft coupled to drive means at its upper end and a vaned rotor at its lower end. Gas under sufficient pressure to be injected into the melt is fed into a passageway extending axially through the device whereby upon rotation of the rotor the gas is injected into the molten metal and subdivided into discrete gas bubbles.
- the process of the invention utilizes the above described gas injection apparatus for refining molten aluminum by introducing an inert gas into the metal beneaththe surface of the melt.
- This invention relates in general to refining ofmolten aluminum, and more particularly, to a method and apparatus for removing dissolved gases and non-metallic impurities from molten aluminum and its alloys without the emission of corrosive or environmentally harmful gases and fumes.
- Molten aluminum prior to casting contains many impurities which, if not removed, cause high scrap loss in casting, or otherwise cause poor metal quality in products fabricated therefrom.
- the principal objectionable impurities are dissolved hydrogen and suspended non-metallic particles such as the oxides of aluminum and magnesium, refrac-,
- the solubility of hydrogen in aluminum alloys decreases by about an order of magnitude when the metal solidifies. Consequently, hydrogen gas is released from the metal during casting if the hydrogen content of the molten metal is not reduced below the solid solubility limit of hydrogen in the metal. Hydrogen causes pinhole porosity in rapidly solidified metal such as directchill cast ingots, or fills shrinkage cavities in slowly solidified metal. Even hydrogen remaining dissolved in the metal after solidification is harmful, since it diffuses during heat treatment into voids and other discontinuities in the solid metal, therebyaggravating the harmful I effects of these defect points on the properties of the metal. Excessive amounts of hydrogen cause bright flakes in forgings and blisters in rolled products.
- Solid, non-metallic particles suspended in the molten metal cause serious difficulties during casting and fabrication of aluminum alloys.
- These particles consist mainly of oxides which are introduced into the melt with the scrap during the melting operation, or are produced by'direct oxidation with air, water vapor, carbon dioxide and other oxidizing gases while the metal is processed in the molten state.
- Fine, broken-up oxide films stirred into the molten metal are particularly harmful, since in contrast to the more macroscopic oxides and other solid particles they cannot be skimmed off as dross and remain suspended in the molten metal. It has been suggested that buoyancy is provided for these oxide particles by microscopic hydrogen bubbles adsorbed on the particles.
- the term sound metal is used in reference to the quality of the molten metal immediately prior to casting, and is intended to mean that both dissolved hydrogen andnon-metallic impurities are removed from the molten metal to an extent required for the production of substantially flawless cast ings or for fabrication of the particular alloy into a useful metal product.
- the soundness of the metal is determined by conventional testing procedures well known in the art, such as vacuum solidification test of the molten metal before casting, metallographic and ultrasonic examinations of the solid metal according to relevant standards, porosity tests, destructive testing, etc.
- chlorine vaporizes aluminum in the form of aluminum chloride gas, and reacts with substantially all the alloying elements in aluminum alloys. This is undesirable from both an operational as well as economic standpoint. Furthermore, unreacted chlorine gas represents a health hazard for operating personnel. Therefore, the fluxing chamber :is generally operated under negative pressure to prevent leakage of the toxic gas into the atmosphere. This, however, facilitates the entry into the chamber of air and moisture from the surrounding atmosphere which then come into contact with the molten metal. As a result, the metal can be recontaminated with hydrogen and oxygen during and after the fluxing operation.
- inert gases such as nitrogen and argon
- inert gases have been suggested for the fluxing of aluminum and its alloys.
- comparative tests carried out with these inert gases at conditions similar to those used for chlorine fluxing have shown that the inert gases were inferior to chlorine in their fluxing ability, and in addition have caused operational difficulties.
- the problems encountered with the use of inert gas have included a less efficient degree of hydrogen removal, severe splashing of the metal atgas flow rates at which no splashing occurred with chlorine, poor non-metallic impurity removal and a significant increase in the metal content of the dross. I
- porous media has been suggested for the introduction of the inert gas into the metal instead of conventional fluxing tubes. This suggestion was apparently aimed at improving the gas injection technique and, in fact, contributed in some cases to better utilization of the inert gas in removing hydrogen.
- this technique has not gained wide acceptance by the aluminum industry, due to the fact that only at rela-- tively low gas flow rates can porous media efficiently disperse the gas into distinct gas bubbles in molten aluminum, and because at practical gas flow rates the degree of non-metallic impurity removal has been unsatisfactory.
- inert gases introduced through porous materials are used principally for degassing aluminum alloys under special plant conditions, where the production routine and economics justify a relatively slow metal treatment rate.
- OBJECTS Accordingly,it is an object of this invention to provide a device capable of injecting inert gas into a molten metal bath, such as aluminum, in the form of small discrete bubbles at high gas flow rates in such manner as to cause the gas bubbles to come into intimate contact with the entire mass of the molten metal bath.
- a device capable of subsurface injection of gas in the form of small discrete bubbles into a mass of molten metal contained in an enclosure comprising in combination:
- the second aspect of the present invention is a system for refining molten aluminum comprising in com bination: (l) a gas injection device as set forth above, (2) an insulated vessel provided with entrance and exit means for the continuous flow of molten metal through said vessel, means for the discharging of gas from said vessel and (3) a vessel cover which seals said vessel to prevent infusion of air and moisture into said vessel, which enables said vessel to be operated under positive pressure and which has an opening therein into which said gas injection device is inserted in a sealed manner.
- the third aspect of the present invention is a process for removing dissolved hydrogen and non-metallic impurities from molten aluminum prior to casting comprising the steps of:
- inert gas as used herein is meant to include gases which are inert towards molten aluminum. Argon and nitrogen or mixtures thereof are preferred for this purpose although, the inert gases of the periodic table viz., helium, krypton, xenon or mixtures of any of them are also suitable for the present invention.
- aluminum as used throughout the specification and claims ismeant to include pure aluminum metal as well as alloys of aluminum.
- FIG. 1 is a perspective view of a preferred embodiment of the gas injection device of the present invention
- FIG. 2 is a cross-sectional view of the device shown in FIG. 1;
- FIG. 3 is a schematic diagram in cross-section illustrating a preferred system for refining a metal stream in a continuous process in accordance with the present invention
- FIGS. 4 and 5 are a cross-sectional and a top view, respectively, of another preferred embodiment of apparatus suitable for refining molten metal in accordance with the present invention.
- the gas injection device of the present invention is characterized by its ability to inject a gas at high flow rates into molten metal in the form of discrete gas bubbles and to achieve a high degree of gas dispersion throughout the melt.
- the device when in operation, induces flow patterns in the metal in the vicinity of the device such that the gas bubbles which are formed, are
- Such preheating is provided in the present invention by conducting the gas through a passageway running the ,length of the device which is submerged in the hot mol ten metal.
- the initially cold gas is preheated by contact with the hot, heat conducting walls of the gas passageway, whereby the gas is expanded before being subdivided into gas bubbles. Consequently, the number of bubbles generated from a given volume of gas is increased substantially, and thermal growth of the small bubbles in the melt is substantially prevented.
- the injection device of the present invention When used for injecting inert gas into molten aluminum, the injection device of the present invention produces an unanticipated improvement in the efficiency of the refining operation.
- the vigorous stirring action produced by the device coupled with the large gas/metal contact area of the well distributed gas bubbles, assure efficient removal of solid particulate impurities suspended in the melt a major deficiency in the prior art of light metal refining with inert gases.
- the process of the invention can refme aluminum at an efficiency comparable to that achieved with chlorine, while eliminating the problems inherent with chlorine fluxing.
- the gas injection device consists of rotor ll, equipped with vertical vanes 2, and rotated by means of a motor, such as an air motor or electric motor (not shown) through shaft 3.
- Shaft 3 which does not contact the melt during normal operation, may be constructed of steel, while the remainder of the equipment is preferably constructed from a refractory material, such as commercially available graphite or silicon carbide, materials which are inert toward aluminum and its alloys at the operating temperatures involved.
- Shaft 3 is shielded from the molten metal by sleeve 4, which is fixedly attached to stator 5.
- a plurality of vertical channels 11 are machined into stator 5.
- the upper flow pattern 13 has a main velocity vector pointing essentially downward, i.e., it is coaxial with the axis of rotation of the rotor 1, thereby forcing the molten metal through the channels 11 of stator 5;
- the lower, more localized flow pattern indi cated byarrows l2 develops beneath the rotor l and is pointed essentially upward and perpendicular to the axis of rotation of the rotor l.
- the resultant flow of these components is indicated by arrows 14, which 1 show that the molten metal is forcefully discharged by from rotor 1.
- the resultant flow pattern causes a well distributed and uniform gas dispersion and a thorough agitation of the molten metal within the treating vessel.
- An inert gas (indicated by arrow 15), such as argon or nitrogen, is introduced into the annular passageway 10 at a predetermined pressure and flow rate.
- the gas fills the bell shaped pocket 16 which is a continuation of passageway 10 surrounding neck 17 of rotor 1. Since the gas is supplied at a pressure greater than the pressure prevailing in the molten metal at a height indicated by arrow 18, the gas pocket 16 prevents molten metal from running back through the gas passage and from coming in contact with the metal shaft 3 of the gas injector.
- Neck 17 surrounds shaft 3 and is constructed from a material resistant to molten aluminum in order to protect shaft 3 from attack by molten aluminum.
- inert gas 15 into annular passageway 10 need not necessarily be the sole means of providing the gas to be injected.
- An alternate embodiment of the invention may include a hollow shaft, wherein a passageway 19 extends axially through shaft 3 and is provided with a plurality of drillings 20 which provide communication with passageway 10 and gas pocket 16.
- inert gas (indicated by arrows 15 and 25) may be provided through either passageway 10 or passageway 19 or both.
- the cold gas (indicated by arrows l and 25) entering the injector be preheated during its passage through passageway or passageway 19, and gas pocket 16 by contacting the sleeve 4 and shaft 3 which are essentially at the temperature of the melt.
- the preheated gas is forced between the vanes of the rotor l where it is broken up into small discrete bubbles by collision with the vanes 2 and by the metal flow sweeping past the vanes.
- the forced circulation of the metal around the injector device rapidly disperses the gas bubbles as they are formed in a direction essentially along the main flow velocity vector, indicated by arrows M.
- the initial trajectory of the gas bubbles follows the direction of the arrows 14 until the buoyancy force prevails and causes the gas bubbles to rise to the surface of the melt.
- the beneficial effects of the forced circulation pattern of the metal around the injection device include the following: (1) the provision of an efficient mechanism for small gas bubble formation, (2) the prevention of bubble coalescence by dispersing the small gas bubbles almost simultaneously with their formation, (3) the provision of efficient circulation of the metal, and (4) prolonged residence time of the gas bubbles in the melt beyond the time they wouldremain in the melt if gravity were the sold force acting upon them.
- the process of the invention can be carried out in a batch-type operation, or in a continuous operation by using a refining system such as shown in FIG. 3.
- the refining system comprises a cast iron shell 31 which is maintained at its operating temperature by conventional heating means which may be located in well 32, and is insulated against heat loss by an outer refractory shell 33.
- the inner surface of shell 31 is lined with graphite 34 or with other refractory materials which are inert to molten aluminum and non-metallic impurities likely to be present.
- Shell 31 is provided with a cover 36 which rests upon flanges 39.
- a gas-tight seal is provided between flanges 39 and cover 36 which may be bolted or otherwise fastened thereto, thereby allowing the system to be operated without the iltration of air.
- a gas injection device 35 such as that shown in PEG. 3, is fastened to cover 36 and supported therefrom.
- inert gas (indicated by arrow 37) is injected into molten metal 38 by gas injector 35.
- the gas after passing through the molten metal, collects in head space 43 to form an inert gas blanket over the melt and leaves through metal inlet port 40 counter-current to the incoming flow of metal.
- the free cross-sectional area of the gas passage, and hence the pressure in the system, is regulated by damper 49 located in port 40.
- the slightly pressurized inert gas in head space 43 prevents air leakage into the vessel.
- metal inlet port 40 Entry of the metal 38 into the refining system is through metal inlet port 40.
- metal 38 is sparged by the uniformly distributed small bubbles of inert gas and is agitated by the action provided by the rotating gas injector 35. Hydrogen dissolved in the melt diffuses into and is carried away by the bubbles of inert gas as they rise through the melt to the melt surface 42.
- the large surface area of the finely dispersed gas bubbles also serves as an efficient transport means for suspended oxide particles to dross layer 48 at the melt surface 42 from where they can be removed by skimming.
- the major overall circulation pattern developed in the molten metal are schematically shown by arrows 50. It is this induced flow pattern of metal in the vessel which continues to bring fresh metal into contact with the gas bubbles which are being discharged from the space between the rotor and stator of the injection device.
- the refined molten metal leaves the refining vessel through discharge port 44 situated below the metal surface 42 in wall 45.
- the metal then passes through well 46 and leaves the system through exit trough 47 to a casting station.
- Well 46 may contain a conventional filtering medium, such as, graphite or solid refractory chips.
- Skimrning of the metal surface 42 may be accomplished by stopping the inlet flow of metal to the refining vessel while maintaining the flow of inert gas 37 through gas injector 35 so as to push the dross layer 48 into inlet trough 40 from where it may be removed by mechanical means.
- metal surface 42 can be skimmed by means of a hand tool inserted into shell 31 through inlet trough 40 or through an opening (not shown) in cover 3 6.
- the refining operation is not restricted to being carried out in a single refining zone as shown in FIG. 3; rather, the vessel may contain a plurality of individual refining compartments or zones through which the molten metal passes in series.
- FIGS. 4, and 5 illustrate such an alternate arrangement.
- the refining vessel 55 is constructed from a refractory which is inert to molten aluminum, and is insulated against heat losses with high temperature insulating materials. if necessary, the vessel may also be provided with electric heating elements (not shown) to compensate for heat losses.
- Refining vessel 55 is provided with a cover 56 which is attached to vessel 55 gas-tight leaving only the metal inlet trough 57 unsealed.
- Gas injectors 39 and as which are of the type described in FIG. l, and their respective drives 61 and 62 are supported by cover 56. Arrows '75 indicate inert gas entering gas injectors 591 and (MD through their respective inlet ports.
- the refining vessel 55 is intended to be used in continuous operation, i.e., molten metal is continuously supplied through inlet trough 57 into the vessel 55, the metal is refined by continuous agitation and gas injection through injectors 59 and 60, and the refined metal is continuously withdrawn from the vessel via exit trough 58.
- Reference to FIG. 5 shows that refining vessel 55 is provided with two refining zones 63 and 64 separated by a baffle plate 65.
- the metal first enters refining zone 63 where it is agitated and sparged with an inert gas provided by gas injector 59.
- the metal leaves the refining zone 63, in part by overflow over the top of baffle plate 65, and partly by underflow through ports 66 provided in baffle plate 65.
- the metal is further refined in the second refining zone 64 where it is similarly agitated and sparged with inert gas provided by gas injector 60.
- the metal leaves refining zone 64 by overflowing the bottom baffle plate 67 and entering exit pipe 68.
- Exit pipe 68 is fabricated from a refractory material, such as graphite or silicon carbide and serves to conduct the refined molten metal from refining zone 64 to exit well 69 where it leaves the refining vessel through exit trough 58.
- the refining gas introduced into the system passes through the molten metal, collects in head space 74 above the metal and leaves the refining vessel 55 through inlet trough 57 above and in counter-current flow to the entering molten metal.
- the pressure in the refining vessel 55 may be adjusted by a hingeddamper 73, located in inlet trough 57, by regulating the free cross-sectional area of the gas passage in inlet trough 57.
- the degree of refining which is necessary will, of course, vary with the intended use of the cast product.
- the addition of a salt flux may be advantageous during refining to promote oxide-metalseparation.
- the flux is selected from the group consisting of halides of alkali and alkaliearth metals. This chemical flux may be charged into the inlet trough 57 when the flow of metal is initiated through the refining vessel or through a port (not shown) providedin the cover 56.
- the exit well 72 maybe filled with a suitable filtering medium, preferably one having a density lower than that of molten aluminum or its alloys, such as coke or crushed graphite, to insure removal of the flux from the metal as it leaves the refining vessel 55.
- a suitable filtering medium preferably one having a density lower than that of molten aluminum or its alloys, such as coke or crushed graphite, to insure removal of the flux from the metal as it leaves the refining vessel 55.
- An efficient and convenient alternate method of providing an in situ fluxing agent to the bath is the addition of a small amount of chlorine to the inert gas.
- chlorine is introduced into a molten aluminum alloy containing magnesium, part of the chlorine reacts with magnesium forming magnesium chloride, an efficient fluxing agent, the remaining part reacts with aluminumforming aluminum chloride gas.
- magnesium chloride is preferentially formed relative to aluminum chloride, tothe extent that substantially all the chlorine supplied with the inert gas reacts with magnesium. It is therefore possible to generate an effi ient in situ" fluxing agent in magnesium containing aluminum alloys by introducing chlorine into the melt, in a highly diluted form withan inert gas, through the injection device of the present invention.
- concentration of chlorine in the inert gas is generally regulated in the range of O to 5 vplume percent depending upon the magnesium content of the alloy, but in no case is it allowed to exceed the amount which results in the emission of harmful byproducts from the system. 7
- a distinct advantage of the system of the present invention is that it can be readily adjusted to supply the refining gas requirements for different alloy grades and the speed of refining can be matched to a wide range of casting rates.
- the specific refining gas requirement generally expressed as volume of gas at normal temperature and pressure per unit weight of metal to be treated, is a function of the composition of the alloy and the degree of purity required in the finished product.
- the flow rate of metal through the refining system is governed by the required speed of casting, i.e., by the type of casting machines used and by the number of ingots cast simultaneously from the refined metal.
- the following examples illustrate a convenient way by which operating conditions in the system may be adjusted depending upon the particular alloy to be refined and the desired rate of refining in accordance with the present invention. 7
- the flow rate of the refining gas per gas injection device is calculated from the following formula:
- R 300 750V 83r )/d where: R the speed of rotation of the rotor, (RPM);
- V the gas flow rate through the device as calculated from formula( I normal cu.ft./min;
- the least cross-sectional dimension of refining zone 63 is the smaller of the two dimensions indicated by arrows and 71;
- This formula yields an approximate RPM for the rotor which ensures a satisfactory dispersion of the refining gas and a good stirring of the metal bath under most operating conditions. From the formula it can be seen that the speed of the rotor must be increased with increasing refining gas flow rates. It should be noted, however, that it is possible to operate the device at significantly lower speeds than predicted by this formula, the optimum speed being dictated primarily by the desired degree of refining.
- EXAMPLE I 1,640 lbs of alloy selected from the 6,000 series is to be refined in 12 minutes.
- the specific refining gas requirement of the alloy is C 0.0146 normal cu.ft. gas/lb metal.
- the system contains one gas injection device and is characterized by the following dimensional constants:
- the refining rate, W, defined in formula (1) is calculated as W 1,640 lbs/ 12 minutes 137 lbs/min.
- EXAMPLE II A high strength structural alloy selected from the 7,000 series is to be refined in a continuous operation, i.e., while the metal is being transferred to a casting station where several fabricating ingots are cast simultaneously from the refined alloy, at a total rate of 37,000 lbs metal/hour.
- the specific refining gas requirement of the alloy was determined by experimentation as C 0.019 normal cu.ft./lb.
- the system contains two gas injection devices and is characterized by the following dimensional constants:
- the solution of formula 1) yields a gas flow rate of V 5 .86 normal cu.ft./min and, in accordance with formula (2), a satisfactory refining is achieved by rotating the gas injection devices at a speed of 739 RPM.
- the induced circulation pattern is such as to transport the injected gas bubbles in a direction extending radially outward from the axis of said device with a downward component relative to said axis.
- the rotatable shaft contains a second passageway extending axially therethrough and is provided with a plurality of drillings which communicate with said axially extending passageway, formed by the inner surfaces of said sleeve and stator and the outer surface of said shaft, for conveying and discharging said gas into said mass of metal.
- Apparatus for refining molten aluminum comprising in combination: (1) a gas injection device as set forth in claim 1, (2) an insulated vessel provided with entrance and exit means for the continuous flow of molten metal through said vessel, means for the discharging of gas from said vessel and (3) a vessel cover which seals said vessel to prevent infusion of air and moisture into said vessel, which enables said vessel to be operated under positive pressure and which has an opening therein into which said gas injection device is inserted in a sealed manner.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Accessories For Mixers (AREA)
- Waste-Gas Treatment And Other Accessory Devices For Furnaces (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21195071A | 1971-12-27 | 1971-12-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3743263A true US3743263A (en) | 1973-07-03 |
Family
ID=22788934
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00211950A Expired - Lifetime US3743263A (en) | 1971-12-27 | 1971-12-27 | Apparatus for refining molten aluminum |
Country Status (10)
Cited By (85)
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US3839019A (en) * | 1972-09-18 | 1974-10-01 | Aluminum Co Of America | Purification of aluminum with turbine blade agitation |
US3871872A (en) * | 1973-05-30 | 1975-03-18 | Union Carbide Corp | Method for promoting metallurgical reactions in molten metal |
US3892395A (en) * | 1972-09-28 | 1975-07-01 | Foseco Int | Stopper rods |
US3902895A (en) * | 1973-02-09 | 1975-09-02 | Wolfgang Wuth | Method for the treatment of fusible non-ferrous metals, particularly copper, by means of a blowing-on of reaction gases |
US3904180A (en) * | 1973-05-18 | 1975-09-09 | Southwire Co | Apparatus for fluxing and filtering of molten metal |
US3917242A (en) * | 1973-05-18 | 1975-11-04 | Southwire Co | Apparatus for fluxing and filtering of molten metal |
US3972709A (en) * | 1973-06-04 | 1976-08-03 | Southwire Company | Method for dispersing gas into a molten metal |
US4007923A (en) * | 1975-07-18 | 1977-02-15 | Southwire Company | Molten metal filter |
US4040610A (en) * | 1976-08-16 | 1977-08-09 | Union Carbide Corporation | Apparatus for refining molten metal |
US4169584A (en) * | 1977-07-18 | 1979-10-02 | The Carborundum Company | Gas injection apparatus |
US4203581A (en) * | 1979-03-30 | 1980-05-20 | Union Carbide Corporation | Apparatus for refining molten aluminum |
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EP0042196A1 (en) * | 1980-06-12 | 1981-12-23 | Union Carbide Corporation | Apparatus for refining molten metal |
US4357004A (en) * | 1981-07-06 | 1982-11-02 | Union Carbide Corporation | Apparatus for refining molten metal |
FR2506785A1 (fr) * | 1981-05-27 | 1982-12-03 | Sumitomo Light Metal Ind | Appareil pour le traitement de metal fondu |
EP0151434A1 (en) * | 1984-01-25 | 1985-08-14 | Norsk Hydro A/S | Method of and apparatus for treating and breaking up a liquid with the help of centripetal force |
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US4992241A (en) * | 1990-03-15 | 1991-02-12 | Alcan International Limited | Recycling of metal matrix composites |
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GB1428146A (en) * | 1972-09-18 | 1976-03-17 | Aluminum Co Of America | Purification of aluminium |
SE7706137L (sv) * | 1976-06-18 | 1977-12-19 | Union Carbide Corp | Sett att raffinera smelt metall |
JPS5426907A (en) * | 1977-08-02 | 1979-02-28 | Rozai Kogyo Kk | Mixing method of molten metal in aluminum melting furnace |
JPS55105520U (enrdf_load_stackoverflow) * | 1979-01-20 | 1980-07-23 | ||
FR2491954A1 (fr) * | 1980-10-14 | 1982-04-16 | Pechiney Aluminium | Dispositif de traitement d'un bain de metal liquide par injection de gaz |
JPS5731280Y2 (enrdf_load_stackoverflow) * | 1981-01-08 | 1982-07-09 | ||
FR2512067B1 (fr) * | 1981-08-28 | 1986-02-07 | Pechiney Aluminium | Dispositif rotatif de dispersion de gaz pour le traitement d'un bain de metal liquide |
US4738717A (en) * | 1986-07-02 | 1988-04-19 | Union Carbide Corporation | Method for controlling the density of solidified aluminum |
AU2006308469B2 (en) * | 2005-10-25 | 2011-09-08 | Stas Inc. | In-line salt refining of molten aluminium alloys |
JP2020142232A (ja) * | 2019-02-28 | 2020-09-10 | キヤノン株式会社 | ウルトラファインバブル生成方法、ウルトラファインバブル生成装置、およびウルトラファインバブル含有液 |
JP7223725B2 (ja) * | 2020-06-04 | 2023-02-16 | 堺アルミ株式会社 | アルミニウム溶湯処理方法 |
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- 1972-12-26 SU SU721864202A patent/SU1068040A3/ru active
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- 1972-12-26 ES ES410033A patent/ES410033A1/es not_active Expired
- 1972-12-27 NO NO4773/72A patent/NO134754C/no unknown
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Cited By (176)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3839019A (en) * | 1972-09-18 | 1974-10-01 | Aluminum Co Of America | Purification of aluminum with turbine blade agitation |
US3892395A (en) * | 1972-09-28 | 1975-07-01 | Foseco Int | Stopper rods |
US3902895A (en) * | 1973-02-09 | 1975-09-02 | Wolfgang Wuth | Method for the treatment of fusible non-ferrous metals, particularly copper, by means of a blowing-on of reaction gases |
US3904180A (en) * | 1973-05-18 | 1975-09-09 | Southwire Co | Apparatus for fluxing and filtering of molten metal |
US3917242A (en) * | 1973-05-18 | 1975-11-04 | Southwire Co | Apparatus for fluxing and filtering of molten metal |
US3871872A (en) * | 1973-05-30 | 1975-03-18 | Union Carbide Corp | Method for promoting metallurgical reactions in molten metal |
US3972709A (en) * | 1973-06-04 | 1976-08-03 | Southwire Company | Method for dispersing gas into a molten metal |
US4007923A (en) * | 1975-07-18 | 1977-02-15 | Southwire Company | Molten metal filter |
US4040610A (en) * | 1976-08-16 | 1977-08-09 | Union Carbide Corporation | Apparatus for refining molten metal |
US4169584A (en) * | 1977-07-18 | 1979-10-02 | The Carborundum Company | Gas injection apparatus |
US4203581A (en) * | 1979-03-30 | 1980-05-20 | Union Carbide Corporation | Apparatus for refining molten aluminum |
EP0017150A1 (en) * | 1979-03-30 | 1980-10-15 | Union Carbide Corporation | Apparatus for refining molten aluminium |
EP0038608A1 (en) * | 1980-04-21 | 1981-10-28 | Union Carbide Corporation | Apparatus for refining molten metal |
EP0042196A1 (en) * | 1980-06-12 | 1981-12-23 | Union Carbide Corporation | Apparatus for refining molten metal |
US4373704A (en) * | 1980-06-12 | 1983-02-15 | Union Carbide Corporation | Apparatus for refining molten metal |
FR2506785A1 (fr) * | 1981-05-27 | 1982-12-03 | Sumitomo Light Metal Ind | Appareil pour le traitement de metal fondu |
DE3219782A1 (de) * | 1981-05-27 | 1982-12-30 | Sumitomo Light Metal Industries Ltd., Tokyo | Vorrichtung zum behandeln von geschmolzenem metall |
US4401295A (en) * | 1981-05-27 | 1983-08-30 | Sumitomo Light Metal Industries, Ltd. | Apparatus for treating molten metal |
US4357004A (en) * | 1981-07-06 | 1982-11-02 | Union Carbide Corporation | Apparatus for refining molten metal |
EP0069434A1 (en) * | 1981-07-06 | 1983-01-12 | Union Carbide Corporation | Apparatus for refining molten metal |
EP0136394A3 (en) * | 1983-10-06 | 1986-05-07 | Yokosuka Boat Kabushiki Kaisha | Method and apparatus for solution of gas in liquid |
EP0151434A1 (en) * | 1984-01-25 | 1985-08-14 | Norsk Hydro A/S | Method of and apparatus for treating and breaking up a liquid with the help of centripetal force |
US4618427A (en) * | 1984-01-25 | 1986-10-21 | Ardal Og Sundal Verk A.S. | Method of treating and breaking up a liquid with the help of centripetal force |
US4634105A (en) * | 1984-11-29 | 1987-01-06 | Foseco International Limited | Rotary device for treating molten metal |
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Also Published As
Publication number | Publication date |
---|---|
NO134754B (enrdf_load_stackoverflow) | 1976-08-30 |
SU1068040A3 (ru) | 1984-01-15 |
ES414721A1 (es) | 1976-02-01 |
ES414722A1 (es) | 1976-06-16 |
IT974890B (it) | 1974-07-10 |
IN140212B (enrdf_load_stackoverflow) | 1976-09-25 |
IN137552B (enrdf_load_stackoverflow) | 1975-08-16 |
ES410033A1 (es) | 1975-12-01 |
JPS4873314A (enrdf_load_stackoverflow) | 1973-10-03 |
NO134754C (enrdf_load_stackoverflow) | 1976-12-08 |
JPS5236487B2 (enrdf_load_stackoverflow) | 1977-09-16 |
FR2166014A1 (enrdf_load_stackoverflow) | 1973-08-10 |
FR2166014B1 (enrdf_load_stackoverflow) | 1975-03-28 |
ES439938A1 (es) | 1977-03-01 |
AU471539B2 (en) | 1976-04-29 |
CA981912A (en) | 1976-01-20 |
SU982546A3 (ru) | 1982-12-15 |
DE2263288B2 (de) | 1976-06-24 |
DE2263288A1 (de) | 1973-07-12 |
AU4943672A (en) | 1974-05-30 |
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