US2380863A - Improving magnesium-base alloys - Google Patents
Improving magnesium-base alloys Download PDFInfo
- Publication number
- US2380863A US2380863A US459832A US45983242A US2380863A US 2380863 A US2380863 A US 2380863A US 459832 A US459832 A US 459832A US 45983242 A US45983242 A US 45983242A US 2380863 A US2380863 A US 2380863A
- Authority
- US
- United States
- Prior art keywords
- magnesium
- base alloys
- casting
- metal
- cast
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910045601 alloy Inorganic materials 0.000 title description 20
- 239000000956 alloy Substances 0.000 title description 20
- 229910052751 metal Inorganic materials 0.000 description 19
- 239000002184 metal Substances 0.000 description 19
- 238000005266 casting Methods 0.000 description 15
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 12
- 239000007789 gas Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000000155 melt Substances 0.000 description 10
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
- 229910002092 carbon dioxide Inorganic materials 0.000 description 6
- 239000001569 carbon dioxide Substances 0.000 description 6
- 229910002091 carbon monoxide Inorganic materials 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 230000004907 flux Effects 0.000 description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229910000861 Mg alloy Inorganic materials 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000005587 bubbling Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C22B26/00—Obtaining alkali, alkaline earth metals or magnesium
- C22B26/20—Obtaining alkaline earth metals or magnesium
- C22B26/22—Obtaining magnesium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/06—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of magnesium or alloys based thereon
Definitions
- This invention relates to a method of improving the mechanical properties of cast magnesium-base alloys by treatment of the molten metal prior to casting.
- a known process for improving the mechanical properties of cast magnesium-base alloys involves heating the molten metal prior to casting for a controlled period at a temperature well above ordinary casting temperatures, usually at above 1600 F. This treatment, which is frequently termed superheating," effects a grain refinement of the solid metal formed on casting and increases its mechanical properties to a value considerably greater than that of cast metal which has not been superheated.”
- the principal object of the present invention to provide a method of treating molten magnesium-base alloys prior to casting which produces in the cast metal mechanical properties at least as good as those obtained by "superheating" and which at the same a protective saline flux and heated to a casting r temperature, usually to 1300 to 1600 F., in accordance with conventional practice.
- a gaseous oxide of carbon is then introduced into or over the body of molten metal, which is agitated to insure intimate contact between the gas and all parts of the melt. Adequate agitation and contact are most, conveniently attained simply by bubbling a stream of the gas through the molten metal.
- Operation in this manner is continued for a time sufficient to produce the desired improvement in grain structure and properties of the metal after casting but insumcient to produce any substantial thickening of the melt by oxidation of the metal, usually for from 5 to 30 minutes.
- the refined molten alloy is then cast into any desired form in known manner, the resulting article exhibiting a flner grain structure and improved mechanical properties as compared to articles cast from the same alloy without the treatment.
- Carbon monoxide is somewhat rapid in its action
- carbon dioxide is perhaps to be preferred be-- cause of its more ready availability and the fact that no health hazard arises if some of it escapes into the foundry atmosphere.
- the gases are preferably used in a pure or nearly pure state, although they may without serious disadvantages be admixed with air, combustion products, or like gases which are practically inert to magnesium alloys under the conditions of the process. They should, however, be largely free of hydrogen, water vapor, or gaseous hydrocarbons, since these gases may tend to introduce hydrogen into the magnesium alloy and thus to cause porosity in the castings subsequently poured.
- the temperature of the magnesium-base alloy during the gas treatment is not critical, but may be maintained at any convenient value in the ordinary casting range, usually at 1300" to 1600 F.; the higher temperatures in the range permit a somewhat shorter treatment time.
- the rate of addition of the carbon monoxide or carbon dioxide although not critical, is important, and should preferably be relatively high, addition at the rate of at least 0.004 cubic foot of gas per pound of metal per minute for periods of 5 to 20 minutes producing optimum properties in the cast metal.
- the process of the invention is applicable in improving the physical properties of all magnesium-base alloys. It is particularly advantageous in the case of msnesium-base alloys containing from 3 to 10 per cent by weight of aluminum as the major alloy-.
- Example 1 A body oi Downmetal E (a magnesium-base alloy containing 5.8 per cent by weight of aluminum and 0.12 per cent manganese, the balance being magnesium) was melted under a Protective flux and heated to a temperature of 1500' 1'. Carbon dioxide was then bubbled through the melt at a rate of 0.005 cubic foot per pound per minute for' a period of minutes, after which the treated alloy, still at 1500 F., was poured into sand molds. On examination, the metal thus cast was found to have an average grain size 01 0.006 inch, and to exhibit the following mechanical properties: tensile strength, 31,200 pounds per square inch; yield strength, 12,100 pounds per square inch; elongation, in 2 inches, 8.6 per cent.
- tensile strength 31,200 pounds per square inch
- yield strength 12,100 pounds per square inch
- elongation in 2 inches, 8.6 per cent.
- Example 2 A body 01 Dowmetal H (a magnesium-base alloy containing 6.1 per cent aluminum, 3.0 per cent zinc, and 0.11 per cent manganese, balance magnesium) was melted under a protective flux and heated to 1400 F. Carbon monoxide was then bubbled rapidly through the melt for minutes, after which the metal was cast in sand molds. The grain size 01' the resulting cast metal was 0.003 inch, and the mechanical properties were: tensile strength, 31,000 pounds per square inch; yield strength, 14,200 pounds per square inch; elongation, in 2 inches, 6.6 per cent.
- the step which comprises agitating the molten 15 metal in intimate contact with a gaseous oxide 01' carbon for a period suillcient to eli'ect the desired improvement in properties but insuflicient to produce a substantial thickening of the melt.
- the step which comprises maintaining the molten metal at a casting temperature below about 1800 I". and bubbling a stream of a gaseous oxide of carbon through the melt for a period which is at least about 5 minutes but is insulllcient to produce substantial thickening oi the melt.
- a method according to claim 2 wherein the gas mployed is carbon monoxide.
- a method according to claim 2 wherein the alloy treated is a magnesium-base alloy containing from 3 to 10 per cent by weight of aluminum as the major alloying element.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
Patented July 31, 1945 assess: mraovmo macnaswm-aasa ALLOYS Charles E. Nelson and Graydon E. Holdeman, Midland, Mlcln, assignors to The Dow Chemical Company, Midland, Mich a corporation of Michigan No Drawing. Application September 28, 1942, Serial No. 459,882
8 Claims.
This invention relates to a method of improving the mechanical properties of cast magnesium-base alloys by treatment of the molten metal prior to casting.
A known process for improving the mechanical properties of cast magnesium-base alloys involves heating the molten metal prior to casting for a controlled period at a temperature well above ordinary casting temperatures, usually at above 1600 F. This treatment, which is frequently termed superheating," effects a grain refinement of the solid metal formed on casting and increases its mechanical properties to a value considerably greater than that of cast metal which has not been superheated."
While the "superheating" process is eflective for its intended purpose, it is in practice limited in application to the treatment of comparatively small melts, since the requirements of time and fuel needed for heating large bodies of molten alloy at high temperatures and the dimculties of accurately controlling considerable changes of temperature in such bodies render the "superheating" of large melts uneconomic. As a result, the optimum properties of cast magnesium-base alloys resulting from superheating" have for the most part not been attained in large-scale foundry operations and in the pouring of large castings.
In view of these facts it is the principal object of the present invention to provide a method of treating molten magnesium-base alloys prior to casting which produces in the cast metal mechanical properties at least as good as those obtained by "superheating" and which at the same a protective saline flux and heated to a casting r temperature, usually to 1300 to 1600 F., in accordance with conventional practice. A gaseous oxide of carbon is then introduced into or over the body of molten metal, which is agitated to insure intimate contact between the gas and all parts of the melt. Adequate agitation and contact are most, conveniently attained simply by bubbling a stream of the gas through the molten metal. Operation in this manner is continued for a time sufficient to produce the desired improvement in grain structure and properties of the metal after casting but insumcient to produce any substantial thickening of the melt by oxidation of the metal, usually for from 5 to 30 minutes. Following the gas treatment, the refined molten alloy is then cast into any desired form in known manner, the resulting article exhibiting a flner grain structure and improved mechanical properties as compared to articles cast from the same alloy without the treatment.
Either carbon monoxide or carbon dioxide may be used as the treating gas in the invention. Carbon monoxide is somewhat rapid in its action,
but carbon dioxide is perhaps to be preferred be-- cause of its more ready availability and the fact that no health hazard arises if some of it escapes into the foundry atmosphere. The gases are preferably used in a pure or nearly pure state, although they may without serious disadvantages be admixed with air, combustion products, or like gases which are practically inert to magnesium alloys under the conditions of the process. They should, however, be largely free of hydrogen, water vapor, or gaseous hydrocarbons, since these gases may tend to introduce hydrogen into the magnesium alloy and thus to cause porosity in the castings subsequently poured.
The temperature of the magnesium-base alloy during the gas treatment is not critical, but may be maintained at any convenient value in the ordinary casting range, usually at 1300" to 1600 F.; the higher temperatures in the range permit a somewhat shorter treatment time. The rate of addition of the carbon monoxide or carbon dioxide. although not critical, is important, and should preferably be relatively high, addition at the rate of at least 0.004 cubic foot of gas per pound of metal per minute for periods of 5 to 20 minutes producing optimum properties in the cast metal.
In so far as is known, the process of the invention is applicable in improving the physical properties of all magnesium-base alloys. It is particularly advantageous in the case of msnesium-base alloys containing from 3 to 10 per cent by weight of aluminum as the major alloy-.
ing element, with or without lesser proportions of other elements such as manganese, zinc, and silicon.
The following examples will serve to illustrate limiting its scope:
Example 1 A body oi Downmetal E (a magnesium-base alloy containing 5.8 per cent by weight of aluminum and 0.12 per cent manganese, the balance being magnesium) was melted under a Protective flux and heated to a temperature of 1500' 1'. Carbon dioxide was then bubbled through the melt at a rate of 0.005 cubic foot per pound per minute for' a period of minutes, after which the treated alloy, still at 1500 F., was poured into sand molds. On examination, the metal thus cast was found to have an average grain size 01 0.006 inch, and to exhibit the following mechanical properties: tensile strength, 31,200 pounds per square inch; yield strength, 12,100 pounds per square inch; elongation, in 2 inches, 8.6 per cent.
For the sake of comparison, an otherwise identical casting waspoured at 1500 F. from Dowmetal E which had not been treated with carbon dioxide. It exhibited an average grain size of 0.009 inch and mechanical properties as follows: tensile strength, 27,600 pounds per square inch; yield strength, 9,500 pounds per square inch; elongation, 'in 2 inches, 7.4 per cent.
Example 2 A body 01 Dowmetal H (a magnesium-base alloy containing 6.1 per cent aluminum, 3.0 per cent zinc, and 0.11 per cent manganese, balance magnesium) was melted under a protective flux and heated to 1400 F. Carbon monoxide was then bubbled rapidly through the melt for minutes, after which the metal was cast in sand molds. The grain size 01' the resulting cast metal was 0.003 inch, and the mechanical properties were: tensile strength, 31,000 pounds per square inch; yield strength, 14,200 pounds per square inch; elongation, in 2 inches, 6.6 per cent.
A comparative casting poured at 1400" F. from the invention, but are not to be construed as the same alloy before the carbon monoxide treatment had a grain size of 0.006 inch and phy cal properties as follows: tensile strength, 27,600
pounds per square inch; yield strength 10,700 5 pounds per square inch; elongation, in 2 inches,
ill-percent. I
The foregoing description is illustrative rather than limitative, the invention being coextensive in scope with the following claims.
What is claimed is:
1. In a method or improving the mechanical properties 01 cast magnesium-base alloys by treatment or the molten metal prior to casting, the step which comprises agitating the molten 15 metal in intimate contact with a gaseous oxide 01' carbon for a period suillcient to eli'ect the desired improvement in properties but insuflicient to produce a substantial thickening of the melt.
2. In a method of improving the mechanical properties or cast magnesium-base alloys by treatment of the molten metal prior to casting, the step which comprises maintaining the molten metal at a casting temperature below about 1800 I". and bubbling a stream of a gaseous oxide of carbon through the melt for a period which is at least about 5 minutes but is insulllcient to produce substantial thickening oi the melt.
3. A method according to claim 2 wherein the gas mployed is carbon monoxide.
4. A method according to claim 2 wherein the gas employed is carbon dioxide.
5. A method according a claim 2 wherein the gas is introduced into the melt at a rate of at least 0.004 cubic foot per pound of metal per minute.
6. A method according to claim 2 wherein the alloy treated is a magnesium-base alloy containing from 3 to 10 per cent by weight of aluminum as the major alloying element.
CHARLm E. NELSON. GRAYDON E. HOLDEMAN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US459832A US2380863A (en) | 1942-09-26 | 1942-09-26 | Improving magnesium-base alloys |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US459832A US2380863A (en) | 1942-09-26 | 1942-09-26 | Improving magnesium-base alloys |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2380863A true US2380863A (en) | 1945-07-31 |
Family
ID=23826305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US459832A Expired - Lifetime US2380863A (en) | 1942-09-26 | 1942-09-26 | Improving magnesium-base alloys |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2380863A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2436520A (en) * | 1944-05-03 | 1948-02-24 | Reconstruction Finance Corp | Grain refining magnesium alloys |
| US2448993A (en) * | 1944-08-26 | 1948-09-07 | Reconstruction Finance Corp | Grain refining magnesium alloys |
| US2472757A (en) * | 1945-02-16 | 1949-06-07 | Dow Chemical Co | Mechanical method for grain refining magnesium alloys |
| US2540366A (en) * | 1945-03-07 | 1951-02-06 | Aluminum Co Of America | Production of magnesium castings |
| US3975187A (en) * | 1975-02-13 | 1976-08-17 | Reynolds Metals Company | Treatment of carbothermically produced aluminum |
| WO1980001082A1 (en) * | 1978-11-21 | 1980-05-29 | Alusuisse | Purification process of molten aluminum |
-
1942
- 1942-09-26 US US459832A patent/US2380863A/en not_active Expired - Lifetime
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2436520A (en) * | 1944-05-03 | 1948-02-24 | Reconstruction Finance Corp | Grain refining magnesium alloys |
| US2448993A (en) * | 1944-08-26 | 1948-09-07 | Reconstruction Finance Corp | Grain refining magnesium alloys |
| US2472757A (en) * | 1945-02-16 | 1949-06-07 | Dow Chemical Co | Mechanical method for grain refining magnesium alloys |
| US2540366A (en) * | 1945-03-07 | 1951-02-06 | Aluminum Co Of America | Production of magnesium castings |
| US3975187A (en) * | 1975-02-13 | 1976-08-17 | Reynolds Metals Company | Treatment of carbothermically produced aluminum |
| WO1980001082A1 (en) * | 1978-11-21 | 1980-05-29 | Alusuisse | Purification process of molten aluminum |
| US4338124A (en) * | 1978-11-21 | 1982-07-06 | Swiss Aluminium Ltd. | Method of purification of aluminium melts |
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