US2267862A - Removal of iron from magnesiumbase alloys - Google Patents

Removal of iron from magnesiumbase alloys Download PDF

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US2267862A
US2267862A US357788A US35778840A US2267862A US 2267862 A US2267862 A US 2267862A US 357788 A US357788 A US 357788A US 35778840 A US35778840 A US 35778840A US 2267862 A US2267862 A US 2267862A
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iron
manganese
alloy
magnesium
temperature
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Joseph D Hanawalt
Charles E Nelson
Graydon E Holdeman
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Dow Chemical Co
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Dow Chemical Co
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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
    • C22B26/22Obtaining magnesium

Description

1941- J. D. HANAWALT ETAL 2,267,862
REMOVAL OF IRON FROM MAGNESIUM-BASE ALLOYS Filed Sept. 21, 1940 Tempera/we -C 57 U S R 4 M .0? n T wE R my 0 Vflmm ah i? A 5 0 5% Z J (6 m Patented Dec. 30, 1941 7 REMOVAL OF IRON FROM MAGNESIUM- BASE ALLOYS Joseph D. Hanawalt, Charles E. Nelson, and
Graydon E. Holdeman, Midland, Mich., assignors to The Dow Chemical Company, Midland,
Micln, a corporation of Michigan Application September 21, 1940, Serial No. 357,788
14 Claims.
This invention relates to the removal of iron impurities from magnesium and magnesiumbase alloys.
For some time it has been appreciated that the tendency of uncoated articles of magnesium and magnesium-base alloys to corrode on exposure to moist air and to aqueous solutions is insome way dependent upon the presence of traces of iron in the metals. More recently it has been shown that there is a certain minute but critical proportion of iron, e. g. about 0.002 per cent in the case of magnesium-base alloys containing aluminum, below which these metals are highly corrosion resistant, but above which they are relatively corrosible. It is evident, then, that in order to render iron-contaminated magnesium and magnesium-base alloys resistant to attack the iron content thereof must be reduced to below the critical corrosion tolerance limit. Unfortunately, however, since at least part of the iron is in actual physical. solution in the metal when molten many of the removal processes described in the art are ineffective in reducing the iron concentration to a sufliciently low value. The remaining known processes, while more or less effective, are fraught with operating difiiculties and are wasteful of expensive purifying agents. Moreover, the ironfree metal produced by such processesusually cannot be remelted and heated to casting temperatures in iron and steel containers without again becoming contaminated with iron.
It is accordingly an object of'the present invention to provide a simple, convenient, and relatively inexpensive method of treating ironcontaminated magnesium and magnesium-base alloys to reduce the concentration of iron therein to a proportion well below the critical corrosion tolerance limit, 1. e. to below 0.002 'per cent for most alloys. Another object is to provide a method whereby magnesium and alloys thereof containing less than the critical corrosion limitof iron may be heated in contact with surfaces of metallic iron at temperatures up to 925 C; without dissolving iron. Other objects will be apparent from the description.
The present invention depends upon the discovery that iron is virtually insoluble, i. e. solu-- ble to an extent well below 0.002 per cent by weight, in molten magnesium and magnesiumbase alloys when these metals contain manganese in a proportion substantially equal to its solubility limit. For instance, when manganese is dissolved in a molten iron-contaminated magnesium alloy in a quantity approximately sufficient to form a saturated solution, the dissolved iron is rendered insoluble and precipitates, until less than 0.002 per cent remains in solution. The resulting alloy, since it contains ironin a proportion below the critical corrosion limit, is highly corrosion resistant. Likewise, when a substantially iron-free magnesium-base alloy is heated in contact with iron surfaces, if the alloy is nearly saturated with manganese, there is little if any solution of iron from the surfaces into the metal, since the latter is already saturated with iron even though somewhat less than 0.002 per cent is present. The corrosion resistance of the alloy is not reduced.
In removing dissolved and suspended iron impurities from magnesium and magnesium-base alloys according to the invention, any of a variety of essentially similar procedures may be employed. In general, the metal to be purified is melted, ordinarily under a suitable protective in a proportion approximately equal to its solubility limit at a predetermined temperature below 925 C., such operation being carried out at a temperature at least as high as the predetermined temperature. Aftef'solution is complete, the temperature of the molten metal is then controlled at the predetermined temperasame without agitation,
ture,- whereby a substantially saturated solution of manganese is formed without appreciable precipitation of metallic manganese, and the dissolved iron is rendered insoluble and precipitates. This precipitate may then be separated from the molten metal, usually by maintaining the and preferably also without permitting the temperature to fall appreciably, for a time sufficient topermit the iron to settle out of solution. However, other separation methods, such as centrifuging, are entirely possible.
In the invention, .the introduction of manganese into the magnesium or magnesium-base alloy may be accomplished by any suitable method. Thus, 'metallic manganese may be melted together with the magnesium, or stirred into the already molten metal. Alternatively, reducible manganese compounds, especially binary compounds such as manganous chloride, manganous fluoride, manganous oxide, manganese dioxide, etc., may be brought into contact with the molten magnesium,ias by incorporating the compound in the protective melting'flux, whereby the compound is reduced, forming manganese which dissolves in the magnesium. All these methods are comprehended by the term dissolving manganese in the metal, as herein e ployed.
The precise proportion of manganese required to form a substantially saturated solution with I any given alloy and at any desired separation temperature may easily be determined by simple experiment. Typical solubility data are given in the accompanying drawing, which illustrates graphically the variation with temperature of the limiting solubility-of manganese in molten magnesium, and in certain alloys of magnesium with aluminm. Inasmuch as alloyingelements other than aluminum do not affect the manganese solubility markedly, the graph will also serve as a rough guide for adding manganese rendered insoluble and precipitating. The metal is then maintained without agitation fora time sufficient for the precipitated iron, and also any suspended iron particles initially present as such, to settle out of the metal, usually for 30 minutes or more to insure complete settling. After this,
the purified metal is separated from the settled iron, as by decanting, and may be. introduced into a casting mold wherein it is allowed to solidify. As stated, the dissolving, settling, and
casting are all conductedwhile maintaining the metal at a substantially constant temperature, which is usually well above 700 C. to permit successful casting, although temperatures as low as 650 C. are operable. The resulting cast metal contains dissolved ironin' an amount less than 0.002 per cent by weight. It may be remelted in iron containers and heated. to temperatures as high as the original operating temperature without dissolving iron from-the container.
In an alternative form of the invention, the
settling and casting operations are carried-out at a substantially constant temperature in the range 650 C. to 925 C., but the dissolving of manganese is carried out at any desired higher temperature. In this case, manganese is incorporated in the heated molten metal in a proportion just suflicient-to form a saturated solution at the subsequent lower settling temperature, the precise proportion being determined'by the reference to a solubility diagram as explained. When the manganese is completely dissolved in the desired proportion, the.
melt is then cooled to the settling temperature, whereby a substantially saturated solution is formed, and the dissolved iron precipitates, and may be removed by means hereinbefore set forth.
As already stated, the process of the invention depends upon maintaining the molten magnesium or magnesium-alloy substantially saturated with manganese at the temperature of settling. In the case of constant temperature operation, it is sometimes convenient to attain this result simply byadding an excess of manganese to the settling vessel. In general, howe'ver,'it is-highly preferable to avoid the presence of any substantial excess undissolved manganese. In this way, waste of expensive metal iseliminated and the heating problems resulting-from the presence of metallic sludge are obviated, and in addition the corrosive attack by manganese on the iron and steel settling vessels ordinarily used is largely prevented. To avoid the presence of excess manganese, it is desirable to control quite carefully the quantity of manganese or reducible manganese compound added to the molten metal to be purified so as to approximate closely the satu- In this instance, iron-contaminated magnesium is melted under a protective flux, and aluminum is alloyed therewith in the predetermined proportion. Minor quantities of other alloying ele-, ments, such as zinc, cadmium, silicon, or tin, may also be added if desired. When this operation is completed, manganese or a reducible manganese compound is added to the heated melt in a quantity sufiicient to dissolve manganese in the alloy in the predetermined proportion. The temperature of the resulting alloy is then controlled to approximately that temperature in the range between about 650 C.'and about 925 C. at which the solubility limit of manganese in the final alloy is equal to the proportion of manganese added. In this way, the alloy is rendered substantially, saturated with manganese without appreciable precipitation thereof, and the dis solved iron impurities become insoluble and precipitate, and may be removed as hereinbeforeexplained. .This method of operation, in which the aluminum is added to the magnesium prior t0 the introduction of themanganese, is advantageous in that the proportion of the aluminum can be carefully controlled, as by rapid hardness iron-contaminated tests, without interference by the presence of manganese. It is within the invention, however,
to add the alloying elements, including manganese, in any desired order, or together.
Thus far it has been assumed that inthe process described the dissolving of manganese and the settling and casting steps are all carried out indirect sequence without allowing the metal to cool below its' saturation temperature. However, there is another procedural sequence which.
also utilizes the principle of the invention; In
this latter case, the iron-contaminated magne-- sium or magnesium-base alloy is melted and manganese dissolved therein in a proportion substantially equivalent to its solubility limit at any desired predetermined temperature above 650 C., preferably in the range 725? C. to 850 C.
The molten metal is then poured directly without a settling period into an ingot moldand allowed to solidify. The resulting ingot may then be stored .or shipped, and -.remelted for casting at any later-time. The melt so formed may then be heated without agitation to a castingtemperature' not appreciably above the predetermined manganese-saturation temperature.- In
this way, because the magnesiumissaturated with manganese,, the iron-impurities present in settle'out on the bottom of the remelting pot.
The melt may then be separated from the settled iron. as by decanting, and cast into molds to form finished products containing less than 0.002 per cent iron. This method of operation has the advantage that the metal maybe heated at high temperatures, i. e. up to 925 0., prior to casting the ingot to efiect a grain refinement, which persists even after the remelting and final casting operations.
In addition-to all the foregoing, of the invention may also .be applied to those instances in which it is desired to melt purified magnesium or magnesium-base alloy already containing less than 0.002 per cent by weight of iron in an iron vessel at temperatures between about 700 C. and about 925 C., particularly above 725 C.,'without experiencing contamination of the purified metal. This result may be attained merely by dissolving and maintaining in the molten metal a proportion of manganese sumcient to form a saturated solution at the temperature of heating. Because of the manganese saturation, solution of iron from the vessel into the alloy is substantially prevented, and the high corrosion resistance of the purified alloy is not destroyed.
The following examples will serve further to illustrate the invention, but are not to be construed as limiting its scope.
Example 1 Commercial metallic magnesium was melted under a protective flux having the following composition in per cent by weight: potassium chloride, 55; barium chloride, 9; magnesium chloride,
34; calcium fluoride, 2. The molten metal was heated to a temperature of 800 C., and metallic aluminum and metallic zinc were then stirred into the melt in quantities sufficient to form an alloy containing 9.0 per cent aluminum and 0.7 per cent zinc. The iron content of this alloy was found to be 0.037 per cent. Manganese was then dissolved in the melt in the proportion of 0.92 per cent, by stirring into the protective flux a sufficient quantity of a saline mixture consisting of manganese chloride, ,72 per cent; potassium chloride, 23 per cent; barium chloride, 2.5 per cent; and calcium fluoride, 2.5 per cent. The resulting alloy, which was substantially saturated with manganese, was then maintained without agitation at 800 C. for two hours, during which time the iron impurities, rendered insoluble by the presence of manganese, settled out .as a sludge. The purified alloy was then decanted from the sludge and poured into ingot molds to solidify. The resulting ingots contained only 0.0007 per cent iron, and were highly resistant to corrosion by moist air and by salt water. They could be remelted in iron containers at temperatures up to 800 C. or slightly higher without any observable increase in iron content.
Example 2 v Commercial magnesium was melted under a protective flux as in Example 1, and heated at a temperature of 785 C. while sufficient finelydivided metallic manganese was stirredinto the melt to form a solution containing 2.0 per cent by weight of manganese. The resulting alloy, which was found to contain 0.0126 per cent iron, was cooled to 700 C., at which temperature it became substantially saturated with manganese,
. the original alloy remain insoluble, and do not dissolve during the remelting operation, but
the principle e 3 and was held at that temperature without agitation for two hours, during which time the iron impurities settled out of the alloy. At the end of the period, less than 0.0007 per cent of iron remained dissolved in the metal.
Example 3 Commercial magnesium, metallic aluminum, and metallic manganese were melted'together at 700 C. under a protective flux to form an alloy containing 10.0 per cent aluminum and 0.5 per' Example 4 Dowmetal R, a magnesium-base alloy contain ing 9.0 per cent aluminum, 0.7 per cent zinc, and 0.2 per cent manganese, the balance being magnesium, was melted under a protective flux and heated to 800 C. Sufiicient metallic manganese to form a saturated solution at that temperature was stirred into the molten alloy, which was then 0.0015 iron, and exhibited immediately poured into ingot molds and allowed tosolidify. The resulting ingots contained 0.004 per cent of iron as impurity. The ingots were later remelted under flux in a steel pot and heated slowly without agitation to a, temperature of 3300 C. During the remelting, the iron impurities present settled out of the alloy. The purified metal was then decanted from the settled iron and cast into billets, which were found to contain less than 0.001 per cent iron.
Example 5 Dowmetal H, a magnesium-base alloy containnesium, was melted under aprotective flux, and
metallic manganese was dissolved in the metal in a proportion corresponding to its solubility limit at 750 C. The resulting melt was heated with stirring at temperaturesin the range 890 C. to 925 C. for a short period, and then immediately cast into ingots, which were found to contain 0.030 per cent iron as; impurity. The ingots were later remelted and heated without agitation at, 750 C. for a time suflicient to permit the iron impurities, which were insoluble at that temperature, to settle out. The settled alloy was then cast into billets. The latter contained the characteristicgrain refinement resulting from the high temperature treatment given.
From the discussion, it will be evident that the invention provides a simple and successful meth- 0d of removing iron impurities from magnesium and its alloys to values less than its critical. corrosion limit. The method does not employ an excess of an expensive purifyingingredient, is not wasteful of heat, and substantiallyeliminates corrosion of iron and steel containers employed.
Moreover, the purified alloy may be remelted at casting temperatures in iron pots without an observable increase in iron content. The method also provides a particularly convenient way of forming iron-free aluminumand manganesecontaining magnesium-base alloys.
It is to be understood that the foregoing description is illustrative rather than strictly 1imitative, and that the invention is co-extensive in scope with the following claims.
1., Themethod of removing dissolved iron 'impurities from iron-contaminated molten magnesium and magnesium-base alloys which comprises: adding to the, molten metal a suflicient quantity of a substance selected from the 'class consisting of manganese and reducible manganese compounds to form in the molten metal. a solution containing manganese in a proportion approximately equal to its solubility limit in the metal at a predetermined temperature between about 650 C. and about 925 C., while maintaining the metal at a temperature at least as high as the predetermined temperature; then controlling the temperature of the metal at approxi-' mately the predetermined temperature, whereby a substantially saturated solution of manganese in the metal is formed with'out appreciable precipitation of metallic manganese, and the dissolved iron is rendered insoluble and, precipitates; and separating the molten metal from the precipitated iron while still maintaining approximately the predetermined temperature.
2.- The method of. removing dissolved iron impurities from iron-contaminated molten mag ne sium and magnesium-base alloys which com- P I adding to the molten metal a substance selected'from the class consisting of manganese.
and reducible manganese compounds in a proportion at least suflicient to form in the metal a solution substantially saturated with manganese,
while-maintaining the metal at a substantially constant operating temperature below about 925 0., whereby the dissolved iron is rendered insoluble and precipitates; and thereafter separating the precipitated iron from the molten metal while it is still at the said operating temperature. 3. .The method of removing dissolved iron impurities from molten magnesium and magnesiumbase alloys which comprises: stirring the molten metal and adding thereto a substance selected from the class consisting of manganese and reducible manganese compounds in a quantity sufficient to form a solution containing manganese in a proportion approximatelyequal to its solubility limit in the metal at a predetermined temperature between about 650 C. and about 925 C. while maintaining the metal at a temperature at least as high as the predetermined temperature;
- discontinuing stirring and maintaining the metal without agitation at about the predetermined temperature, whereby there is formed a substantially saturated solution of manganese in the metal, and the dissolved iron is rendered insoluble and settles out of the molten metal; and separating the purified molten metal from the settled iron while still maintaining approximately the predetermined temperature.
4. In a method of forming castings comprising less than 0.002 per cent by weight of iron from molten magnesium and magnesium-base alloys containing dissolved iron' as an impurity, the steps which include: adding to the molten metal a substance selected from the class consisting of manganese and reducible manganese compounds in a proportion approximately equal to but not in excess of that required to form in the metal a solution substantially saturated with manganese,
wherein it is allowed to solidify, said dissolving,
separating, and casting operations all being car-.-
. proximately the said "whereby the dissolved iron is rendered insoluble the molten manganese in ried out" at a substantially constant temperature in the range 925 C.
5. In a method of preparing a substantially iron-free manganeseand aluminum-containing magnesium-base alloy from a. molten iron-contaminated aluminum-containing magnesiumbase alloy, the steps which comprise: adding to alloy manganese supplied in a proportion approximately equal to its solubility limit in the alloy at a predetermined temperature between about 650 C. and about 925 C., said proportionbeing between about 0.2 and about 2.0
between about 650, C. and about per cent by weight; controlling the temperature of the alloy to about said predetermined temperature, whereby a substantially saturated solution of manganese in the alloy is formed without appreciable pre ipitation of metallic manganese, and the dissol ed iron is rendered insoluble and precipitates; and separating the molten alloy from the precipitated iron while still maintaining approximately the predetermined temperature.
6. Ina method of preparing a magnesiumbase alloy containing less than 0.002 per cent .by weight of iron and comprising aluminum and manganese in predetermined proportions between about 0.2 and about 12 per cent of aluminum and between about 0.2 and about 2.0 per cent of manganese, the steps which comprise: forming a molten magnesium-base alloy portions; controlling the temperature of the alloy .thus formed to approximately that temperature tion of manganese, whereby there is formed a .molten alloy substantially saturated with man ganese in the desired proportion, and the dissolved ironis rendered insoluble and precipitates without appreciable precipitation of metallic manganese; and separating the molten alloy from the precipitate while still maintaining aptemperature.
7. In a method of preparing a magnesium-base alloy containing less than 0.002 per cent by weight of iron and comprising aluminum and predetermined proportions .between about 0.2 and about 12 per cent of aluminum'and between about 0.2 and about 2.0
per cent of manganese, the steps which com- I prise: providing a body of molten magnesium therewith in the predeand alloying aluminum termined proportion; adding to the resulting-alloy a substance selected from the class consisting of manganese and reducible manganese compounds in a quantity suflicient to dissolve m'anganese in the alloy in the predetermined proportion; controlling the temperature-of the alloy thus formed to perature in the range about 925 manganese termined desired proportion of manganese, whereby there is formed a molten alloy substantially saturated with manganese in the desired between about 650 C. and C. at which the solubility limit of proportion, and the dissolved iron is rendered insoluble and precipitates; and separating the molten alloy from the precipitate while still maintaining approximately the said temperature. '8. In a method of preparing a magnesium base alloy containing'less than 0.002 per cent by weight of} iron and comprising aluminum and. manganese in predetermined proportions between about containingmanganese and aluminum in the aforesaid proapproximately that temin the alloy is equal to the prede 0.2 and. about 12 per cent of proportion; controlling the temperature of the alloy thus formed to approximately that temperature in the range-between about 650 C. and about 925 C. at which the solubility limit of manganese in thealloy is' equal to the added proportion of manganese, whereby there is formed a molten alloy substantially saturated with manganese in the desired proportion, and the dissolved iron is rendered insoluble and, precipitates without appreciable precipitation of metallic manganese; and separating the molten in the alloy in the predetermined v metal a solution containing manganese in a proportion approximatelyequal to its solubihtylimit at the predetermined remelting temperature,
and thereafter without settling introducing. the
resulting alloy into a mold wherein it is allowed to solidify.
121 In a method of preparing a magnesium base alloy casting containing less than 0.002 per cent by weight of iron from an ingot of an ironcontaminated magnesium-base alloy containing manganese in a proportionsubstantially equal to its solubility-limit in the alloy at a predetermined temperature above 700 C.; the steps which comprise melting the ingot and heating the same without agitation to a castingtemperature not substantially above the predetermined temperature, whereby a substantially saturated solution of manganese in the alloy is formed and alloy from the precipitate while still maintaining approximately the said temperature.
9.'In a method of preparing,
predetermined remelting temperature, and thereafter without settling introducing the resulting alloy into a mold wherein it is allowed to solidify.
10. A process according to claim 9 wherein the molten metal is heated to a temperature sufliciently high to efiect grain refinement prior to introducing it into the mold. v
11. In a method of preparing, from a molten iron-contaminated magnesium-base alloy, an ingot capable of being remelted -and settled in an iron container at a predetermined temperature between about 650 C'. and about 925 C. to form a molten alloy containing less than 0.002 percent by weight of iron, the steps which comprise: adding to the molten iron-contaminated alloy a substance selected from the class consisting of manganese and reducible manganese compounds in a proportion suficient to but not in excess of that required to form in the a proportion" limit at the from a molten iron-contaminated magnesium-base alloy, an inbetween about (00 the iron-impurities remain-insoluble and settle out of the molten alloy; separating the alloy from the settled iron without allowing themetal to cool appreciably; and introducing the purified alloy into a mold wherein it is allowed to solidify.
13. In a method of preparing a magnesiumbase alloy casting containing less than 0.002
per cent by weight of iron from an ingot of an iron-contaminated magnesium-base alloy containing manganesein a proportion substantially equal to its solubility limit in the alloy at apredetermined temperature above 700 'C.;' the steps which comprisemelting'the ingot and heating the same without agitationto a casting temperature substantially equal to ,the predetermined temperature, whereby a substantially saturated solution of manganese in the alloy is formed and the iron-impurities remain insoluble and settle out of the molten alloy without appreciable precipitation of metallic manganese; separating the alloy from the settled iron without allowing the metal to cool appreciably; and introducing the purified alloy into a mold wherein it is allowed to solidify.v I
14. In a process wherein a magnesium-base alloy initially containing less than 0.002 per cent by weight or iron is heated at a temperature C. and about 925 C. in contact with. metallic iron, the method of preventing solution of iron in the molten metal which compriseslmaintaining therein a proportion of manganese sufflcient to form a substantially -saturated solution at the temperature of heating.
' JOSEPH D. HANAWAL'I'.
CHARLES E. NELSON.
GRAYDON' E. HOLDEMAN.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2474538A (en) * 1944-06-10 1949-06-28 Charles H Mahoney Alloying manganese with magnesium
US2497529A (en) * 1945-03-22 1950-02-14 Magnesium Elektron Ltd Process for production of magnesium base alloys containing zirconium
US2497537A (en) * 1946-05-17 1950-02-14 Magnesium Elektron Ltd Zirconium carrying alloying substance
US2500912A (en) * 1944-12-20 1950-03-14 Crimora Res And Dev Corp Method of making alloys
US2575273A (en) * 1947-12-05 1951-11-13 Bendix Aviat Corp Process for producing a magnesium die-casting alloy
US2620270A (en) * 1950-04-03 1952-12-02 Dow Chemical Co Method of improving magnesium and the binary magnesium-base alloy of magnesium and manganese
US2671039A (en) * 1946-05-02 1954-03-02 Bendix Aviat Corp Magnesium die casting alloy and process

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2474538A (en) * 1944-06-10 1949-06-28 Charles H Mahoney Alloying manganese with magnesium
US2500912A (en) * 1944-12-20 1950-03-14 Crimora Res And Dev Corp Method of making alloys
US2497529A (en) * 1945-03-22 1950-02-14 Magnesium Elektron Ltd Process for production of magnesium base alloys containing zirconium
US2671039A (en) * 1946-05-02 1954-03-02 Bendix Aviat Corp Magnesium die casting alloy and process
US2497537A (en) * 1946-05-17 1950-02-14 Magnesium Elektron Ltd Zirconium carrying alloying substance
US2575273A (en) * 1947-12-05 1951-11-13 Bendix Aviat Corp Process for producing a magnesium die-casting alloy
US2620270A (en) * 1950-04-03 1952-12-02 Dow Chemical Co Method of improving magnesium and the binary magnesium-base alloy of magnesium and manganese

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