US1814072A - Separating volatile metals by sublimation - Google Patents
Separating volatile metals by sublimation Download PDFInfo
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- US1814072A US1814072A US80520A US8052026A US1814072A US 1814072 A US1814072 A US 1814072A US 80520 A US80520 A US 80520A US 8052026 A US8052026 A US 8052026A US 1814072 A US1814072 A US 1814072A
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- 229910052751 metal Inorganic materials 0.000 title description 45
- 239000002184 metal Substances 0.000 title description 45
- 150000002739 metals Chemical class 0.000 title description 19
- 238000000859 sublimation Methods 0.000 title description 14
- 230000008022 sublimation Effects 0.000 title description 14
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 17
- 229910052749 magnesium Inorganic materials 0.000 description 17
- 239000011777 magnesium Substances 0.000 description 17
- 238000000926 separation method Methods 0.000 description 14
- 238000000034 method Methods 0.000 description 13
- 239000007787 solid Substances 0.000 description 13
- 229910052708 sodium Inorganic materials 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 7
- 229910052791 calcium Inorganic materials 0.000 description 7
- 239000011575 calcium Substances 0.000 description 7
- 238000001704 evaporation Methods 0.000 description 6
- 239000012535 impurity Substances 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 239000000306 component Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Chemical compound CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 241001446467 Mama Species 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 241000212342 Sium Species 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- PGTXKIZLOWULDJ-UHFFFAOYSA-N [Mg].[Zn] Chemical compound [Mg].[Zn] PGTXKIZLOWULDJ-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 239000012809 cooling fluid Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000000260 fractional sublimation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003385 sodium Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000005092 sublimation method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
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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
- C22B9/02—Refining by liquating, filtering, centrifuging, distilling, or supersonic wave action including acoustic waves
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- This invention relates to the purificationof metals by sublimation or evaporation, and has for its object broadly the separation of the volatile components of im ure metals and alloys.
- I provlde a method of effecting substantial or partial separation of the volatile components .of alloys of the alkali and alkaline earth metals; especially magnesium.
- any sultable apparatus may be used, as for example one of the type described in my copending application above mentioned, to which reference may be made for a more complete description.
- the condenser is preferably of upright cylindrical form, ,equlpped with a split lining-of sheet metal which may be taken out for convenient removal of the metal deposited thereon.
- a lining bearin the deposit of metal on its inner surface, is s own in the accompanying drawings, in which Fig. 1 is a cross section on line 1-1 of Fig. 2, and Fig. 2 is a longitudinal section on line 2--2 of Fig.1 1.
- the sheet metal lining or liner 10 is split longitudinally as indicated at 11.
- the or stalline metal deposit is indicated at 12. he 75 temperature conditions which must be maintained in the condenser are of prime importance. If only one volatile metal is present it is only neoessar to maintain a condenser surface cold enoug I to cause the metal vapor to condense. When, however, two or more volatile metals are present a spatial separation can be effected, that is, the two metals can be caused to deposit on different zones of the condenser surface by maintaining these zones at different and successively lower temperatures, which are kept constant in any given run.
- One effective way of securing the proper temperature gradient on the condenser surface is to so proportion the length of the 90 condenser, with respect to the temperature and heat input in the retort connected therewith, that the natural thermal conduction of heat from the retort to the condenser through its walls, in conjunction with the radiation or other cooling of the conden'lsl ler,
- xternal insulating, heating, and cooling de-' vices of any convenient kind may also be employed for the purpose, enabling the tem- 10c perature to be regulated by manual control, or, if desired, automatically, as by thermostatic means.
- Sod1um may commonly occur as an impurity in magnesium prepared by electrolytic reduction from an electrolyte 1 containing sodium salts, and its removal is usually desirable.
- a suitable charge say 100 pounds of crude magnesium containing about 0.5 per cent sodium, may be placed in the retort and heated under a pressure of about 0.5 to 0.2 mm.
- the metal vapors crystallize on the split liner which is removable from the condenser and which may therefore be taken out and opened.
- the deposit usually has its eatest thickness a short distance from the ottom and from that point tapers ofi' gradually, and it may extend the full len h of the liner. At the extreme upper end t e'deposit may be only about one-sixteenth of an inch thick.
- the adhering crystalline deposit appears uniformly bright and silvery.
- An exposure to the air of about 10 to 20 minutes darkens a zone at the upper end, say down to about the point indicated by the arrow 13.
- Toward the lower edge of the zone-the darkening becomes less noticeable and disappears at a sharply marked boundary, and I have observed the remarkable fact that this boundary is generally so sharply defined that a drop of phenolphthalein solution placed on the line turns distinctly red on the dark side and remains unchanged in color on the bright slde of the deposit.
- Analysls of the material above the line discloses as high as 85 per cent sodium in the deposit at the extreme upper end.
- otassium is somewhat more volatile than sodium but its behavior is similar in the sublimation process and it is readily separable from magnesium by the present process.
- Calcium may also'be purified by my process, with separation of the volatile impurities such as sodium and potassium.
- a charge of pounds of impure calcium was heated in the retort at temperatures which eventually rose almost to the melting point, which is about 810 C., and the metallic calcium was deposited in zones in the condenser with the more volatile impurities segregated at the upper end.
- the concentration of alkali metal at the upper end of the condenser was so high that parts of it ignited on opening the condenser and exposing the deposit to. the air.
- the line of demarcation between the calcium and the more volatile impurities was indicated by a change in color on exposure to the atmosphere for a short time, much as in the case of the magnesium previously described. It is impossible to test with phenolphthalein, however, since the indlcator turns pink when in contact with either the calcium or the alkali metal.
- the temperature gradient in the condenser should be maintained substantially constant and may be regulated in any convenient manner, as for example by the simple expedient of one or more cooling .coils around the condenser at appropriate points, through which the flow of water or other cooling fluid can be controlled in accordance with the interior temperatures as indicated by thermometers suitably located.
- Thermostatic regulation may be employed if automatic control is desired.
- the condenser should not be too short, or the results will not be satisfactory. In sublimingmagnesiuni or calcium at the rate of about 80 pounds in 8-10 hours or so, a cylindrical condenser about four feet long and fourteen inches in diameter'inside has been found satisfactory.
- the time of heating and the rate of evaporation are also factorsin determining the extent of separation of the volatile metals. If the sublimation is too rapid there is greater tendency for the more volatile metals to be included in the deposit at the lower end of the condenser because the rate of condensation there is too rapid to admit of the ready re-evaporation of the small amounts (of the more volatile metal or metals) which are always condensing in that part of the condenser. The period of heating should therefore be snfliciently long to permit the desired separation to be effected in the particular condenser employed. This and other factors are best determined by'experience with the particular mixture or alloy to be treated.
- the pressure in the retort is maintained above the vapor pressure at the melting point of the metal 1n the retort, as by means of an lnert gas or gases, for ex ample argon, in the retort and condenser, or
- a process of subliming impure mag-- sium are produced, the step of condensing said vapors directly to the solid state in a condenser by controlling the temperature conditions in the condenser so as to cause substantial concentration of the solid metals in different parts of the condenser.
- a process of separating alkali metal from impure magnesium or magnesium al- 10y comprising subliming the volatile com ponents under reduced pressure and condensing the magnesium directly to solid form on a surface the temperature of which is maintained above the point of volatilization of the alkali metal but below the sublimation point of magnesium and condensing the alkali metal directly to solid form on a surface of suitably lower temperature.
- a process of subliming compositions containingalkali and alkaline earth metals under reduced pressure comprising subliming the volatile components and condensing the metallic vapors directly to the solid state by passing vapors over a condensing surface while maintaining on the latter a temperature gradient ranging from below the sublimation point of the least volatile metal and above the sublimation point of the more volatile' metal or metals to a suitably lower temperature.
- a process of separating volatile metal constituents of a metallic mixture comprising heating the mixture to volatilize the metals to be separated, and condensing the metallic vapors directly to the solid state by passing the vapors over a condensing surface of decreasing temperature while maintaining the temperature gradient substantially constant.
- a process of separating volatile metal constituents of a metallic mixture comprising heating the mixture to volatilize the metals to be separated, passin the metal vapors into the heated end of a tubular condenser, and regulating the escape of heat from'the condenser to provide therein a sub stantially constant temperature gradient from the hotter to the cooler end and thereby causing the volatilized metals to condense directly to the solid form on the surface of the tubular condenser in the order of their boiling points and with substantial spatial separation.
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- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
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Description
July 14, 1931. i H. E. BAKKEN 1,814,072
SEPARATING VOLATILE METALS BY- SUBLIMATION Filed Jan. 11, 1926 llyz.
Sodium- I Magnesizzm- Snvemtoz mama July 14,1931
UNITED STATES PATENT orrlcs m. BARKER, or NIAGARA FALLS, NEW Yonx, ASSIGNOR 'ro AmnnIcAN MAG- Nnsrou CORPORATION, or NIAGARA FALLS, NEW YORK, A CORPORATION or New YORK snrAnArI'Nq VOLATILE MErALs BY sunLInm'rIoN 4 Application filed January 11, 1926. Serial No. 80,520.
This invention relates to the purificationof metals by sublimation or evaporation, and has for its object broadly the separation of the volatile components of im ure metals and alloys. In particular, I provlde a method of effecting substantial or partial separation of the volatile components .of alloys of the alkali and alkaline earth metals; especially magnesium.
In a copending application, Serial No. 598,292, which has matured into Patent 1,594,344 dated August 3, 1926, I have disclosed a commercial maesium from relatlvely non-volatile impurlties by sublimation. Magnesium commonly has volatile impurities present also, as
for example sodium, which evaporate with it durin sublimation and may contaminate the sublimed' product. I have discovered, go however, that by proper control of the conditions surrounding condensation of the metal vapor, separation of the volatile components of the mixture or allo may also be effected. In my process ofsu limation the metal to as be subhmed is heated in a retort to which is attached a condenser and accessory apparatus for producing a high vacuum in the system.
In operation the pressure in the retort and condenser is reduced below the vapor pressure so of the metal at the temperature to which it is to be heated for sublimation and heat is a plied to the retort. The non-volatile S11E- stance's remain in the retort and the volatile metal eva rates and is de osited on the walls of the con enser. In my a ove-mentioned a plicationI have disclosed the fact that to o tain rapid sublimation, it is desirable to regulate or so adjust the operating pressure 1n the condenser that the vapor pressure of the solid metal in the retort is slightly greater than the total absolute pressure within the condenser. Under these conditions the evolution of metal va or will be rapid, and if the proper condensatlon facilities are provided, the rate of sublimation is limited only by the rate of evaporation of the solid metal. The temperature at which the vapor pressure of the solid metal becomes greater t an the absolute ressure of the system is hereinafter called esublimation point. By operating rocess of separatingv will maintain the desired conditions.
at or above the sublimation point, I not only produce rapid sublimation but I'also sweep out and away the residual amounts of air or other gases in the apparatus and thus decrease the possibility of these gases to combine with and thus introduce non-metallic impurities into the product.
In carrying out my present invention any sultable apparatus may be used, as for example one of the type described in my copending application above mentioned, to which reference may be made for a more complete description. The condenser is preferably of upright cylindrical form, ,equlpped with a split lining-of sheet metal which may be taken out for convenient removal of the metal deposited thereon. Such a lining bearin the deposit of metal on its inner surface, is s own in the accompanying drawings, in which Fig. 1 is a cross section on line 1-1 of Fig. 2, and Fig. 2 is a longitudinal section on line 2--2 of Fig.1 1.
The sheet metal lining or liner 10 is split longitudinally as indicated at 11. The or stalline metal deposit is indicated at 12. he 75 temperature conditions which must be maintained in the condenser are of prime importance. If only one volatile metal is present it is only neoessar to maintain a condenser surface cold enoug I to cause the metal vapor to condense. When, however, two or more volatile metals are present a spatial separation can be effected, that is, the two metals can be caused to deposit on different zones of the condenser surface by maintaining these zones at different and successively lower temperatures, which are kept constant in any given run. One effective way of securing the proper temperature gradient on the condenser surface is to so proportion the length of the 90 condenser, with respect to the temperature and heat input in the retort connected therewith, that the natural thermal conduction of heat from the retort to the condenser through its walls, in conjunction with the radiation or other cooling of the conden'lsl ler,
xternal insulating, heating, and cooling de-' vices of any convenient kind may also be employed for the purpose, enabling the tem- 10c perature to be regulated by manual control, or, if desired, automatically, as by thermostatic means. As one specific illustration of-my inven- 5 tion, I will describe the separation of magnesium from sodium by my fractional sublimation process. Sod1um may commonly occur as an impurity in magnesium prepared by electrolytic reduction from an electrolyte 1 containing sodium salts, and its removal is usually desirable. A suitable charge, say 100 pounds of crude magnesium containing about 0.5 per cent sodium, may be placed in the retort and heated under a pressure of about 0.5 to 0.2 mm. of mercury for a period of approximatel 12 hours, maintaining a temperature of a out 600 C. in the retort, and keeping the upper end of the condenser at about 90 C. The metal vapors crystallize on the split liner which is removable from the condenser and which may therefore be taken out and opened. The deposit usually has its eatest thickness a short distance from the ottom and from that point tapers ofi' gradually, and it may extend the full len h of the liner. At the extreme upper end t e'deposit may be only about one-sixteenth of an inch thick.
When the liner is first removed, the adhering crystalline deposit appears uniformly bright and silvery. An exposure to the air of about 10 to 20 minutes darkens a zone at the upper end, say down to about the point indicated by the arrow 13. Toward the lower edge of the zone-the darkening becomes less noticeable and disappears at a sharply marked boundary, and I have observed the remarkable fact that this boundary is generally so sharply defined that a drop of phenolphthalein solution placed on the line turns distinctly red on the dark side and remains unchanged in color on the bright slde of the deposit. Analysls of the material above the line discloses as high as 85 per cent sodium in the deposit at the extreme upper end. This sodium content decreases as the boundry is approached, being from 1 to 2 per cent adjacent to the boundary, just above the region of bright crystals. An average analysis of the material below the line shows sodium to 'be present in amounts less than 0.05 per cent. As the volatilized metal vapors impinge on the walls of the condenser the atoms of magnesium tend to condense because of the lower temperature in the condenser. At the lower (or warmer) end of the condenser, the temperature is relatively high compared with that at the other end. The more volatile so- 'diumtherefore does not condense on, or else evaporates readily from, the relatiyely hot lower surface and is carried on'farther up the condenser to a cooler zone- When the temperature of-the condensing surface is above' the boiling point of sodium at the pressure in ture of the condensing surface falls below this boiling point, the concentration of the sodium be ms to build up rapidly.
otassium is somewhat more volatile than sodium but its behavior is similar in the sublimation process and it is readily separable from magnesium by the present process.
Calcium may also'be purified by my process, with separation of the volatile impurities such as sodium and potassium. In one example, which I may cite, a charge of pounds of impure calcium was heated in the retort at temperatures which eventually rose almost to the melting point, which is about 810 C., and the metallic calcium was deposited in zones in the condenser with the more volatile impurities segregated at the upper end. The concentration of alkali metal at the upper end of the condenser was so high that parts of it ignited on opening the condenser and exposing the deposit to. the air. The line of demarcation between the calcium and the more volatile impurities was indicated by a change in color on exposure to the atmosphere for a short time, much as in the case of the magnesium previously described. It is impossible to test with phenolphthalein, however, since the indlcator turns pink when in contact with either the calcium or the alkali metal.
In some cases it may be impossible to efiect a very sharp separation of the volatile metals because of their physical characteristics. I have found, for example, that if magnesiumzinc alloys are sublimed, both metals volatilize. The zinc is appreciably more volatile than the magnesium but is, nevertheless, usually found in appreciable butnon-uniform quantities throughout the magnesium deosit. I have also found it impractical to efect a substantially complete separation of calcium and magnesium ,from each other. Even in these andother cases where complete or substantially complete separation cannot be accomplished a useful separation of the constituents may be obtained.
As previously stated, the temperature gradient in the condenser should be maintained substantially constant and may be regulated in any convenient manner, as for example by the simple expedient of one or more cooling .coils around the condenser at appropriate points, through which the flow of water or other cooling fluid can be controlled in accordance with the interior temperatures as indicated by thermometers suitably located. Thermostatic regulation may be employed if automatic control is desired. In some cases it may be desirable to enclose more or less of the condensing column in a heat-insulating jacket or the like, including or excluding the cooling coil or coils, to con trol the escape of heat by convection and radiation and obtain a steeper gradient between adjoining temperature zones; though it is to be understood that anything like a sharp differentiation is unnecessary. The condenser should not be too short, or the results will not be satisfactory. In sublimingmagnesiuni or calcium at the rate of about 80 pounds in 8-10 hours or so, a cylindrical condenser about four feet long and fourteen inches in diameter'inside has been found satisfactory.
The time of heating and the rate of evaporation are also factorsin determining the extent of separation of the volatile metals. If the sublimation is too rapid there is greater tendency for the more volatile metals to be included in the deposit at the lower end of the condenser because the rate of condensation there is too rapid to admit of the ready re-evaporation of the small amounts (of the more volatile metal or metals) which are always condensing in that part of the condenser. The period of heating should therefore be snfliciently long to permit the desired separation to be effected in the particular condenser employed. This and other factors are best determined by'experience with the particular mixture or alloy to be treated.
In carrying out the invention by evaporation of the metal in the liquid state, that is,
by distillation, the pressure in the retort is maintained above the vapor pressure at the melting point of the metal 1n the retort, as by means of an lnert gas or gases, for ex ample argon, in the retort and condenser, or
by throttling the retort outlet, and heat is supplied at a rate sufficient to produce melting, in whole or in part, of the contents of the retort. However, when operating by distillation a higher retort temperature is necessary, and the use of a foreign gas is usually inconvenient'if not otherwise undesirable.
It is to be understood that the invention is not limited to the specific procedure herein described but can be carried out in other ways without departing from its spirit.
1. Process of treating alkali'and alkaline earth metals and alloys thereof, comprising evaporating the metals from a metallic mixture containing the same, and condensing the resulting metallic vapors directly to the solid state upon condensing surface by passing the vapors over such surface while controlling the temperature of said surface so as to cause substantial spatial separation of the metals condensed thereon.
2. A process of subliming impure mag-- sium are produced, the step of condensing said vapors directly to the solid state in a condenser by controlling the temperature conditions in the condenser so as to cause substantial concentration of the solid metals in different parts of the condenser.
3. In a process of subliming impure magnesium or magnesium alloy containing another volatile metal capable of condensing from vapor directly to the solid state, the step of maintaining on a condensing surface to receive the magnesium, zones of successively lower and substantially unvarying temperatures whereby different condensible metals, as they condense directly to the solid state, are concentrated in different zones of the condensing surface.
4. A process of separating alkali metal from impure magnesium or magnesium al- 10y, comprising subliming the volatile com ponents under reduced pressure and condensing the magnesium directly to solid form on a surface the temperature of which is maintained above the point of volatilization of the alkali metal but below the sublimation point of magnesium and condensing the alkali metal directly to solid form on a surface of suitably lower temperature.
5. A process of subliming compositions containingalkali and alkaline earth metals under reduced pressure, comprising subliming the volatile components and condensing the metallic vapors directly to the solid state by passing vapors over a condensing surface while maintaining on the latter a temperature gradient ranging from below the sublimation point of the least volatile metal and above the sublimation point of the more volatile' metal or metals to a suitably lower temperature.
6. A process of separating volatile metal constituents of a metallic mixture, comprising heating the mixture to volatilize the metals to be separated, and condensing the metallic vapors directly to the solid state by passing the vapors over a condensing surface of decreasing temperature while maintaining the temperature gradient substantially constant.
7. A process of separating volatile metal constituents of a metallic mixture, comprising heating the mixture to volatilize the metals to be separated, passin the metal vapors into the heated end of a tubular condenser, and regulating the escape of heat from'the condenser to provide therein a sub stantially constant temperature gradient from the hotter to the cooler end and thereby causing the volatilized metals to condense directly to the solid form on the surface of the tubular condenser in the order of their boiling points and with substantial spatial separation. 1
In testimony whereof I hereto aflix my signature.
HERMAN E. BAKKEN.
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| Application Number | Priority Date | Filing Date | Title |
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| US80520A US1814072A (en) | 1926-01-11 | 1926-01-11 | Separating volatile metals by sublimation |
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| US80520A US1814072A (en) | 1926-01-11 | 1926-01-11 | Separating volatile metals by sublimation |
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Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2425705A (en) * | 1945-08-17 | 1947-08-12 | Dominion Magnesium Ltd | Method of removing manganese from calcium |
| US2434775A (en) * | 1943-05-08 | 1948-01-20 | Sosnick Benjamin | Process for making foamlike mass of metal |
| US2464767A (en) * | 1945-09-06 | 1949-03-15 | Dominion Magnesium Ltd | Production of calcium |
| US2650085A (en) * | 1945-08-24 | 1953-08-25 | Ici Ltd | Apparatus for the purification of calcium |
| US3476547A (en) * | 1966-10-20 | 1969-11-04 | Gen Motors Corp | Method of making metal powder |
| US5658367A (en) * | 1995-09-14 | 1997-08-19 | Reactive Metals & Alloys Corporation | Method of manufacturing magnesium powder from magnesium crown |
| US20130052076A1 (en) * | 2010-05-04 | 2013-02-28 | Andrew Chryss | Separation method |
| US20150232964A1 (en) * | 2014-02-20 | 2015-08-20 | Guizhou Province Product Quality Supervision And Inspection Institute | Method of purifying sodium metal |
-
1926
- 1926-01-11 US US80520A patent/US1814072A/en not_active Expired - Lifetime
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2434775A (en) * | 1943-05-08 | 1948-01-20 | Sosnick Benjamin | Process for making foamlike mass of metal |
| US2425705A (en) * | 1945-08-17 | 1947-08-12 | Dominion Magnesium Ltd | Method of removing manganese from calcium |
| US2650085A (en) * | 1945-08-24 | 1953-08-25 | Ici Ltd | Apparatus for the purification of calcium |
| US2464767A (en) * | 1945-09-06 | 1949-03-15 | Dominion Magnesium Ltd | Production of calcium |
| US3476547A (en) * | 1966-10-20 | 1969-11-04 | Gen Motors Corp | Method of making metal powder |
| US5658367A (en) * | 1995-09-14 | 1997-08-19 | Reactive Metals & Alloys Corporation | Method of manufacturing magnesium powder from magnesium crown |
| US20130052076A1 (en) * | 2010-05-04 | 2013-02-28 | Andrew Chryss | Separation method |
| US10035078B2 (en) * | 2010-05-04 | 2018-07-31 | Commonwealth Scientific And Industrial Research Organisation | Separation method |
| US20150232964A1 (en) * | 2014-02-20 | 2015-08-20 | Guizhou Province Product Quality Supervision And Inspection Institute | Method of purifying sodium metal |
| US9540710B2 (en) * | 2014-02-20 | 2017-01-10 | Guizhou Province Product Quality Supervision And Inspection Institute | Method of purifying sodium metal |
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