US2650085A - Apparatus for the purification of calcium - Google Patents

Apparatus for the purification of calcium Download PDF

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US2650085A
US2650085A US686959A US68695946A US2650085A US 2650085 A US2650085 A US 2650085A US 686959 A US686959 A US 686959A US 68695946 A US68695946 A US 68695946A US 2650085 A US2650085 A US 2650085A
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calcium
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condensing
iron
distillation
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Burnett Robert Le Grice
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Imperial Chemical Industries Ltd
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B26/00Obtaining alkali, alkaline earth metals or magnesium
    • C22B26/20Obtaining alkaline earth metals or magnesium

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  • This invention relatesA to improvements inthe purification of calcium.
  • a process for the puriication of calcium containing an alkali metal as impurity comprises distilling the impure calcium in the presence of an inert gas at an absolute pressure not.V greater than 2 mm. of mercury, condensing, substantially pure calcillin on a condensing surface of, iron ora ferrous alloy and. condensing the alkali metal on a separate condensingl surface, the twofcondensing surn faces beine maintained atsuitalclc temperatures by separate cooling means, advantageously, in order to obtain substantially pure calcium in a readily divided forrn, thedistillationof the calcium is eiected at an absolute pressure between 0.5, and. 2,-@ hun. of mercury..
  • porising metal which; is in the lower par-t of said still, andV condensing means in the upper part of the said still formed of two condensing surfaces, one above the other at a substantial vertical distance apart, tlievlower condensing surface extending lacross the major portion of the cross-section of the still but leaving a space between its periphery and the Walls of the still through which vapour canv ascend, means being provided for maintaining the lowerof the. two surfaces at a temperature. at. which calcium Will condense thereon, and for maintaining the upper condensing surface at a temperature such that the alkali metal will condense titten-zon,v
  • the lower condensing surface is maintained during the earlier part of the distillation at such. a temperature that the calcium will condense thereon lout not the alkali metal- Throughout the distillation this condensingsurface should be maintained at a temperature which will ensure that the calcium is deposited in the desired readily divided iforrn; thus the tempera,- ture of thecalciumcovered surface on which further calcium is being deposited must not be allowed to rise to Stich. anV extent that fusion of the calcium takes place.
  • the ferrous condensing surface may be maintained at Li503 C. to 500@ Cu but as distillation proceeds and the thickness of they condensed calcium increases, it may become necessary to cool the condensing surface further, soV that the freshly formed surf face of the calcium is.
  • the ierrous metal surface may he cooled to .259 C ⁇ to 390
  • the alkali metal-conf taining impure product irorn the high purity calcium- It is thus. rnucheasier to obtain a high purity productirec .zan alkali metal than has been the case with processes used hitherto, and moreover this he vom Without subjectine the product to.
  • an iron-containing layer on the surface of the calcium in contact with the condensing surface depends upon the material of which this surface is composed. Thus if a condensing surface of iron or mild steel is used, the calcium in contact therewith absorbs a signincant proportion of iron, forming a skin which must be removed after the completion of the distillation. However, when a stainless steel condensing surface is used, the iron absorption is so insignificant as to render this step of the process unnecessary.
  • the iron-containing layer can readily be removed by mechanical means, as for example, by scraping; in many cases it can be prised 01T by merely inserting a chisel or the like under the skin. Thus by treating the condensed metal to remove such skin before grinding, milling or otherwise destroying the shape in which it is produced, a metal of correspondingly greater purity can be obtained.
  • the apparatus comprises a stainless steel vessel adapted to contain the crude calcium in the lower portion while the upper portion has a cover which can be attached to the vessel in an air-tight manner and which carries a hollow member extending downwards into the upper portion of the vessel comprising the still, the bottom of the hollow member being a flat plate of mild steel, stainless steel, or other suitable ferrous metal extending over susbtantially the whole cross-section of the still but leaving a narrow space between its periphery and the walls of the still through which vapours not condensing thereon can rise to the upper condensing surface.
  • This plate constitutes the surface on which the high purity calcium can be condensed.
  • a closed pipe or channel is attached to the hollow part depending from the cover, and means are provided for circulating water at high velocity through the pipe or channel.
  • the interior of the hollow member is tted, between the level of the condenser plate and the level of the pipe through which water can flow, with a number of radially disposed iins to increase the heat radiating surfaces of this condenser; means are also provided for circulating air or other suitable cooling medium over these radiating surfaces.
  • heating means for cal--g cium in the lower part of the still which is suitably a fused salt bath in which the still can be immersed to the level of the condenser plate.
  • the upper part of the still is connected to a pump by which the still can be evacuated, means also being provided for measuring the pressure within the still and for supplying thereto an atmosphere or argon or other inert gas.
  • the calcium is obtained in the form of small crystals which are joined loosely together and thus can be broken up in a mill to give high purity calcium in a divided form.
  • the lower part of the still should be at a temperature of the order of 850 C. to 950 C., say at 900 C. to 910 C., while the condensing surface for high purity calcium should be maintained initially at a temperature between 450 C. and 500 C.
  • a much lower temperature should be maintained in the region of the water-cooled pipe or channel, the temperature at this portion of the still being of the order of 30 C. to 60 C.
  • the product removed by this method consists of high quality material, and the layer containing the iron is left on the condenser surface and can be removed separately before the still is used again.
  • Figure 1 is a vertical section and Figure 2 is a plan view taken on the line II-II of Figure 1.
  • a still comprising a stainless steel vessel l, ls supported in a fused salt bath 3 @n feet 4,
  • the top of the vessel is closed by a cover 5, which carries a hollow member 6 extending downwards into the upper part of the still and terminating in a nat steel plate 'I occupying almost the whole of the cross section of the still.
  • a number of radially disposed metal fins 6 are situated in the interior of the hollow member 6, and a flat metal ring 9, fitted with a water cooling coil I0, is attached to the outside of said member about half-way between the cover 5 and the plate 7.
  • a pipe I I supplies compressed air to the fins 8 inside the hollow member, and a pipe I2, leading into the upper part of the still, and capable of being closed by a valve I3, is connected to a vacuum pump and pressure gauge and an inert gas supply, which are not shown in the drawing. Further water cooling coils are provided at I4, and thermocouple pockets at I5 and I6.
  • the still I is then evacuated by means of the pump connected to the pipe I2, and a small amount of argon is introduced through the same pipe so that the absolute pressure within the vessel is between 0.5 and 2 mm. of mercury. As distillation proceeds some occluded gas may be evolved and it is therefore necessary to observe the pressure within the vessel from time to time and if necessary to pump out gas and to introduce an appropriate quantity of argon.
  • the still I is lowered into the salt bath 3, maintained at a temperature of 900 C. to 950 C., so that the surface of the fused salt is level with the condenser plate 1.
  • the still I is raised out of the fused salt bath and allowed to cool, and argon is introduced into the still until the pressure therein is equal to atmospheric pressure.
  • the still is then opened, the condenser plate 1 withdrawn, and the deposited calcium removed therefrom, the iron-containing skin, if present, being subsequently removed from the product, which is then ground to give substantially pure calcium in the form of small crystals.
  • Example Ga Na, Ol, Fe, M-U, percent percent percent percent p. p. m. p. p. m.
  • the distillation was carried out in the manner described above, the calcium being condensed on a mild steel plate, whose temperature was maintained initially at 500 C. and gradually reduced to 250 C.
  • An apparatus for use in the purification of calcium containing an alkali metal as an impurity which comprises a still, means for maintaining therein an inert gas at a reduced pressure, means for vaporising metal which is in the lower part of said still, a removable cover for said still, a tubular member carried by and extending downwards from said cover, a lat horizontal ferrous plate closing the lower end of said tubular member and occupying almost the whole cross section of the still but leaving a space between its periphery and the wall of the still through which vapour can ascend, said plate constituting a lower condensing surface, internal ns in said tubular member, means for circulating a cooling medium over said fins whereby said plate is maintained at a temperature at which calcium will condense thereon, a at horizontal ring carried by said tubular member in the space between itself and the wall of said still, said ring constituting an upper condensing surface, a pipe coil on said ring, and means for circulating a cooling medium through said pipe coil whereby said

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  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
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  • Manufacturing & Machinery (AREA)
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Description

Patented Aug. 25, 1953 ArpARAzl-ios Fon THE PURIFICATIQN oF CALCIUM Robert Le Grice Burnett, Overton, England, as-Y signor to Imperial Chemical Industries Limitedf ,a .corporation of Great Britain Application July 29, 1946, Serial No. 686,959 In Great Britain August 24, 1945 l l Claim.
This invention relatesA to improvements inthe purification of calcium. v
It has already beenv proposed to purify calcium and magnesium, and alloys thereof, by heating the said metal or alloy to cause its rapid vaporisation While subjected to an absolute pressure less than the vapour pressure of the metal or alloyat. its nieltiin,`r point, and condensing the vapours in a suitable manner. Such a process has been described in British specification No. 270,060. Advantaeecusly the pressurewas not more than about. 2 min.. of mercury, and the metallic product was condensed on two heini-cylinolricall seo-V tions of a remcvablclincr placed in the condenser with its axis verticalt Indistillinc metal containing small amounts ci sodium or other impurities more volatile than the inetal or alloy, it was found that they deposit of metal which formed:- on the interior surface, ci the liner ccntained an upper portion relatively rich in the sodium or other impurity. While the lower portion wasY metal or alloylof high purity. `By exposing the. product to air a darkening of the. surface of that portion rich in sodium occurreiiy and this served as an indication oi the place. to separate the pure metal fromthe impure. Such a, process could normally be carried out in. a metallic apparatus, conveniently an apparatus of iron` orsteel.
According to the presenty invention, a process for the puriication of calcium containing an alkali metal as impurity comprises distilling the impure calcium in the presence of an inert gas at an absolute pressure not.V greater than 2 mm. of mercury, condensing, substantially pure calcillin on a condensing surface of, iron ora ferrous alloy and. condensing the alkali metal on a separate condensingl surface, the twofcondensing surn faces beine maintained atsuitalclc temperatures by separate cooling means, advantageously, in order to obtain substantially pure calcium in a readily divided forrn, thedistillationof the calcium is eiected at an absolute pressure between 0.5, and. 2,-@ hun. of mercury..
l have. found that in distillinsv calcium inY this manner, when usine a. condensing surface corn- Posed ci iron or oi. certain. .ferr ns. alloys thereis formed on vthe surface or, rnetal in contact with the condensing suriace a thin layer or skin kwhich contains a. .sienicantprcportion of iron and which. can. readily he rencor/ed hy inea chan-ical means- According to a further Yfeature of the invention therefore. the substantially pure o lcium condensate .is separated icyv mechanical., .means iroin an iron-cont,airlineA layer formed. on the surface thereof contact with the icrrous.. dcnsine suriacee l cium oxidey as impurity- A convenient apparatusy for carrying out the production of high quality calcium from calf ciuin containing an: alkali metal as impurity by the process of the present invention corn-- prises a still, meansV for maintaining therein an inert gas at a reduced pressure, means for va-... porising metal which; is in the lower par-t of said still, andV condensing means in the upper part of the said still formed of two condensing surfaces, one above the other at a substantial vertical distance apart, tlievlower condensing surface extending lacross the major portion of the cross-section of the still but leaving a space between its periphery and the Walls of the still through which vapour canv ascend, means being provided for maintaining the lowerof the. two surfaces at a temperature. at. which calcium Will condense thereon, and for maintaining the upper condensing surface at a temperature such that the alkali metal will condense titten-zon,v
In use the lower condensing surface is maintained during the earlier part of the distillation at such. a temperature that the calcium will condense thereon lout not the alkali metal- Throughout the distillation this condensingsurface should be maintained at a temperature which will ensure that the calcium is deposited in the desired readily divided iforrn; thus the tempera,- ture of thecalciumcovered surface on which further calcium is being deposited must not be allowed to rise to Stich. anV extent that fusion of the calcium takes place. Initially the ferrous condensing surface may be maintained at Li503 C. to 500@ Cu but as distillation proceeds and the thickness of they condensed calcium increases, it may become necessary to cool the condensing surface further, soV that the freshly formed surf face of the calcium is. kept at that temperature, For example, after the. distillation has heen proceeding for about an hour, the ierrous metal surface may he cooled to .259 C` to 390 By using the process of. 'the present lill/@ile tion for the distillation oi calcium@ 1 ain able to eiiect a segregation ci the alkali metal-conf taining impure product irorn the high purity calcium- It is thus. rnucheasier to obtain a high purity productirec .frein alkali metal than has been the case with processes used hitherto, and moreover this he donc Without subjectine the product to. atmospheric oxidation which wouldy necessarily entail theintroduction of cal- Furthermore, when using an apparatus of the type described herein, I rind that amuch, smaller condensing surface suiiices to collect the calcium than in the apparatus used previously: this, factor is. particularly advantaeeous when the material oi which the calcium condensing surface is composed is such that an iron-containing layer is formed, since the fraction of the calcium which has to be rejected on this account is thereby reduced.
The formation of an iron-containing layer on the surface of the calcium in contact with the condensing surface depends upon the material of which this surface is composed. Thus if a condensing surface of iron or mild steel is used, the calcium in contact therewith absorbs a signincant proportion of iron, forming a skin which must be removed after the completion of the distillation. However, when a stainless steel condensing surface is used, the iron absorption is so insignificant as to render this step of the process unnecessary. The iron-containing layer can readily be removed by mechanical means, as for example, by scraping; in many cases it can be prised 01T by merely inserting a chisel or the like under the skin. Thus by treating the condensed metal to remove such skin before grinding, milling or otherwise destroying the shape in which it is produced, a metal of correspondingly greater purity can be obtained.
In one form of the invention the apparatus comprises a stainless steel vessel adapted to contain the crude calcium in the lower portion while the upper portion has a cover which can be attached to the vessel in an air-tight manner and which carries a hollow member extending downwards into the upper portion of the vessel comprising the still, the bottom of the hollow member being a flat plate of mild steel, stainless steel, or other suitable ferrous metal extending over susbtantially the whole cross-section of the still but leaving a narrow space between its periphery and the walls of the still through which vapours not condensing thereon can rise to the upper condensing surface. This plate constitutes the surface on which the high purity calcium can be condensed. A suitable distance above this condenser plate, for example approximately halfway between the plate and the cover, a closed pipe or channel is attached to the hollow part depending from the cover, and means are provided for circulating water at high velocity through the pipe or channel. The interior of the hollow member is tted, between the level of the condenser plate and the level of the pipe through which water can flow, with a number of radially disposed iins to increase the heat radiating surfaces of this condenser; means are also provided for circulating air or other suitable cooling medium over these radiating surfaces. The
still is also provided with heating means for cal--g cium in the lower part of the still, which is suitably a fused salt bath in which the still can be immersed to the level of the condenser plate. The upper part of the still is connected to a pump by which the still can be evacuated, means also being provided for measuring the pressure within the still and for supplying thereto an atmosphere or argon or other inert gas.
In using such an apparatus for the distillation of calcium I nd that the physical nature of the calcium which is produced depends to a large extent upon the pressure which is maintained within the still during the distillation. If pressures much below 0.5 mm. absolute are maintained, the calcium is produced in the form of long, tough needles which are relatively difficult to break up subsequently if the calcium is required in a divided form. On the other hand, by maintaining within the still argon or other inert gas at an absolute pressure between. 015 and .2
mm., the calcium is obtained in the form of small crystals which are joined loosely together and thus can be broken up in a mill to give high purity calcium in a divided form. In order that distillation may proceed in a suitable manner the lower part of the still should be at a temperature of the order of 850 C. to 950 C., say at 900 C. to 910 C., while the condensing surface for high purity calcium should be maintained initially at a temperature between 450 C. and 500 C. A much lower temperature, however, should be maintained in the region of the water-cooled pipe or channel, the temperature at this portion of the still being of the order of 30 C. to 60 C. By operating the still under these conditions to purify calcium containing small proportions of sodium and other impurities it is found that the calcium is deposited on the surface which is maintained at 450 C. to 500 C. in a state of relatively high purity which is readily broken up subsequently, whereas the product which is deposited in the neighbourhood of the water-cooled channel contains substantially all the sodium originally in the crude calcium` There will be substantially no product on the intermediate portions of the walls of the hollow member carrying the two condensing surfaces, and thus segregation of high purity calcium and impure sodium-containing material results. Not only can high quality calcium be obtained in this manner from technical quality calcium, which may contain of the order of 0.5% to 1% of sodium, but it can also be produced quite successfully from calcium containing as little as 0.2% or as much i as 10% sodium. In addition it is possible to reduce to a matter of a few parts per million the amounts of iron, manganese and silicon which may be present in the crude material.
When distillation is complete the still is raised out of the fused salt bath and left until cold while maintaining the reduced pressure in the still; alternatively an atmosphere of argon may be introduced into the still. When the whole is quite cold and the vacuum has been broken, by introducing argon to a pressure of one atmosphere, the cover is lifted up, thus withdrawing the condensing surfaces with the product attached, and the high purity calcium is removed from the surface on which it has condensed by a hammer and chisel or like method. The product will then be in the form of a mass of glistening crystals which may have an iron-containing skin where it has adhered to the condensing surface. The skin, if present, is then removed by prising it o with a chisel or similar means. Instead of first detaching the product and then removing the skin in this way, it is possible to remove the majority of the calcium only from the condenser plate, leaving a narrow thickness of relatively pure calcium on the bottom of the condenser plate. The product removed by this method consists of high quality material, and the layer containing the iron is left on the condenser surface and can be removed separately before the still is used again.
One form of apparatus suitable for carrying out the process of the present invention is illustrated in the accompanying drawing in which the preferred type of still is shown diagrammatically.
Figure 1 is a vertical section and Figure 2 is a plan view taken on the line II-II of Figure 1.
In the drawing, a still comprising a stainless steel vessel l, ls supported in a fused salt bath 3 @n feet 4, The top of the vessel is closed by a cover 5, which carries a hollow member 6 extending downwards into the upper part of the still and terminating in a nat steel plate 'I occupying almost the whole of the cross section of the still. A number of radially disposed metal fins 6 are situated in the interior of the hollow member 6, and a flat metal ring 9, fitted with a water cooling coil I0, is attached to the outside of said member about half-way between the cover 5 and the plate 7. A pipe I I supplies compressed air to the fins 8 inside the hollow member, and a pipe I2, leading into the upper part of the still, and capable of being closed by a valve I3, is connected to a vacuum pump and pressure gauge and an inert gas supply, which are not shown in the drawing. Further water cooling coils are provided at I4, and thermocouple pockets at I5 and I6.
In carrying out the process by the preferred method using the apparatus illustrated in the drawing, the crude calcium in the form of an ingot, shown at 2, contaminated with sodium, is`
put into the still I, and the cover 5 is attached in an air-tight manner. The still is then evacuated by means of the pump connected to the pipe I2, and a small amount of argon is introduced through the same pipe so that the absolute pressure within the vessel is between 0.5 and 2 mm. of mercury. As distillation proceeds some occluded gas may be evolved and it is therefore necessary to observe the pressure within the vessel from time to time and if necessary to pump out gas and to introduce an appropriate quantity of argon. The still I is lowered into the salt bath 3, maintained at a temperature of 900 C. to 950 C., so that the surface of the fused salt is level with the condenser plate 1. Cold water is then caused to ilow through the cooling coils I and I4, and air is blown through the pipe IIv over the radiating ns 8. Distillation then proceeds, the high quality calcium collecting on the plate 1, which is maintained at a temperature of 450 C. to 500 C. by the air passing over the ns 8, while sodium condensed as a solid impure sodium-containing alloy on the water-cooled ring 9. As the thickness of the deposited calcium increases, the temperature of the plate 1 may be reduced as necessary by increasing the rate of flow of the compressed air.
When the distillation is complete, the still I is raised out of the fused salt bath and allowed to cool, and argon is introduced into the still until the pressure therein is equal to atmospheric pressure. The still is then opened, the condenser plate 1 withdrawn, and the deposited calcium removed therefrom, the iron-containing skin, if present, being subsequently removed from the product, which is then ground to give substantially pure calcium in the form of small crystals.
The following example illustrates but does not limit the invention, all proportions being by weight.
Example Ga, Na, Ol, Fe, M-U, percent percent percent p. p. m. p. p. m.
The distillation was carried out in the manner described above, the calcium being condensed on a mild steel plate, whose temperature was maintained initially at 500 C. and gradually reduced to 250 C.
After completion of the distillation, the still was cooled and the vacuum broken by introducing argon, the condenser plate was withdrawn and the calcium removed therefrom. The iron-containing skin, which had been formed on the surface of the calcium in contact with the mild steel plate, was scraped off the calcium mass, and the latter was then ground, giving a crystalline product of the following composition:
An apparatus for use in the purification of calcium containing an alkali metal as an impurity which comprises a still, means for maintaining therein an inert gas at a reduced pressure, means for vaporising metal which is in the lower part of said still, a removable cover for said still, a tubular member carried by and extending downwards from said cover, a lat horizontal ferrous plate closing the lower end of said tubular member and occupying almost the whole cross section of the still but leaving a space between its periphery and the wall of the still through which vapour can ascend, said plate constituting a lower condensing surface, internal ns in said tubular member, means for circulating a cooling medium over said fins whereby said plate is maintained at a temperature at which calcium will condense thereon, a at horizontal ring carried by said tubular member in the space between itself and the wall of said still, said ring constituting an upper condensing surface, a pipe coil on said ring, and means for circulating a cooling medium through said pipe coil whereby said ring is maintained at a temperature such that the alkali metal will condense thereon.
ROBERT LE GRICE BURNET'I".
References Cited in the ille of this patent UNITED STATES PATENTS Number Name Date 1,814,072 Bakken July 14, 1931 1,814,073 Bakken July 14, 1931 2,028,390 Hanson Jan. 21, 1936 2,231,023 Nelson Feb. 11, 1941 2,309,643 Hansgirg Feb. 2, 1943 2,328,479 Mathieu Aug. 31, 1943 2,330,143 Pidgeon Sept. 21, 1943 2,372,168 Alexander Mar. 27, 1945 2,375,198 Alexander May 8, 1945 2,387,677 Pidgeon Oct. 23, 1945 2,399,180 Girvin et al. Apr. 30, 1946 FOREIGN PATENTS Number Country Date 270,060 Great Britain May 5, 1927 Great Britain Feb. 23, 1942
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Cited By (10)

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US2813017A (en) * 1954-09-03 1957-11-12 Pechiney Prod Chimiques Sa Thermal process for producing alkali metals and magnesium
US2860965A (en) * 1956-06-22 1958-11-18 Pechiney Prod Chimiques Sa Process for producing pure manganese
US3123541A (en) * 1964-03-03 donnell
US3294385A (en) * 1963-04-23 1966-12-27 Dominion Magnesium Ltd Apparatus for forming and removing condensed metal crowns
US3301665A (en) * 1963-04-23 1967-01-31 Dominion Magnesium Ltd Method and apparatus for producing high purity calcium
US3375177A (en) * 1967-05-05 1968-03-26 Autosonics Inc Vapor degreasing with solvent distillation and condensation recovery
US3479252A (en) * 1966-11-14 1969-11-18 Uddeholms Ab Apparatus for the degreasing of articles by means of a solvent
US4973387A (en) * 1982-12-28 1990-11-27 Allied-Signal Inc. Apparatus and method for reducing solvent losses
US5048548A (en) * 1990-02-15 1991-09-17 E. I. Du Pont De Nemours And Company Vapor control system for vapor degreasing/defluxing equipment
US5142873A (en) * 1990-02-15 1992-09-01 E. I. Du Pont De Nemours And Company Vapor control system for vapor degreasing/defluxing equipment

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GB270060A (en) * 1926-03-24 1927-05-05 American Magnesium Corp Improvements in or relating to the art of refining calcium and magnesium and their alloys
US1814073A (en) * 1926-03-10 1931-07-14 American Magnesium Corp Purification of calcium
US1814072A (en) * 1926-01-11 1931-07-14 American Magnesium Corp Separating volatile metals by sublimation
US2028390A (en) * 1933-09-29 1936-01-21 Miles G Hanson Method of producing the alkali metals
US2231023A (en) * 1939-02-23 1941-02-11 Dow Chemical Co Method of treating magnesium
GB543370A (en) * 1940-08-20 1942-02-23 Henri Louis Gentil Improvements in or relating to metallurgic furnaces
US2309643A (en) * 1938-12-24 1943-02-02 Anglo California Nat Bank Sublimation refining
US2328479A (en) * 1941-11-22 1943-08-31 Mathieu Francois Electric oven for high temperatures working under vacuum or under neutral gas
US2330143A (en) * 1941-10-22 1943-09-21 Dominion Magnesium Ltd Method and apparatus for producing magnesium
US2372168A (en) * 1943-03-05 1945-03-27 Metal Hydrides Inc Production of metal hydrides
US2375198A (en) * 1943-03-05 1945-05-08 Metal Hydrides Inc Purification of metals
US2387677A (en) * 1942-04-30 1945-10-23 Dominion Magnesium Ltd Apparatus for producing magnesium
US2399180A (en) * 1943-08-18 1946-04-30 Permanente Metals Corp Sublimation apparatus

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1814072A (en) * 1926-01-11 1931-07-14 American Magnesium Corp Separating volatile metals by sublimation
US1814073A (en) * 1926-03-10 1931-07-14 American Magnesium Corp Purification of calcium
GB270060A (en) * 1926-03-24 1927-05-05 American Magnesium Corp Improvements in or relating to the art of refining calcium and magnesium and their alloys
US2028390A (en) * 1933-09-29 1936-01-21 Miles G Hanson Method of producing the alkali metals
US2309643A (en) * 1938-12-24 1943-02-02 Anglo California Nat Bank Sublimation refining
US2231023A (en) * 1939-02-23 1941-02-11 Dow Chemical Co Method of treating magnesium
GB543370A (en) * 1940-08-20 1942-02-23 Henri Louis Gentil Improvements in or relating to metallurgic furnaces
US2330143A (en) * 1941-10-22 1943-09-21 Dominion Magnesium Ltd Method and apparatus for producing magnesium
US2328479A (en) * 1941-11-22 1943-08-31 Mathieu Francois Electric oven for high temperatures working under vacuum or under neutral gas
US2387677A (en) * 1942-04-30 1945-10-23 Dominion Magnesium Ltd Apparatus for producing magnesium
US2372168A (en) * 1943-03-05 1945-03-27 Metal Hydrides Inc Production of metal hydrides
US2375198A (en) * 1943-03-05 1945-05-08 Metal Hydrides Inc Purification of metals
US2399180A (en) * 1943-08-18 1946-04-30 Permanente Metals Corp Sublimation apparatus

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