US2306592A - Beryllium alloy - Google Patents
Beryllium alloy Download PDFInfo
- Publication number
- US2306592A US2306592A US406532A US40653241A US2306592A US 2306592 A US2306592 A US 2306592A US 406532 A US406532 A US 406532A US 40653241 A US40653241 A US 40653241A US 2306592 A US2306592 A US 2306592A
- Authority
- US
- United States
- Prior art keywords
- beryllium
- titanium
- alloy
- oxygen
- zirconium
- 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
- 229910000952 Be alloy Inorganic materials 0.000 title description 2
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 44
- 229910052790 beryllium Inorganic materials 0.000 description 43
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 26
- 239000010936 titanium Substances 0.000 description 26
- 229910052719 titanium Inorganic materials 0.000 description 26
- 229910045601 alloy Inorganic materials 0.000 description 25
- 239000000956 alloy Substances 0.000 description 25
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 18
- 229910052760 oxygen Inorganic materials 0.000 description 18
- 239000001301 oxygen Substances 0.000 description 18
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 15
- 229910052726 zirconium Inorganic materials 0.000 description 15
- 239000012535 impurity Substances 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 9
- 239000002184 metal Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 6
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 238000005098 hot rolling Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt 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
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000003245 working effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C25/00—Alloys based on beryllium
Definitions
- the present invention is directed to the provision of a novel alloy which has substantially the same desirable physical characteristics as beryllium, but is much more malleable and ductile so that under suitable conditions, it may be readily worked into forms suitable for practical use.
- the melting is carried on under a high vacuum, of the order of 0.001 mm. of mercury, and by high frequency currents induced in the metal by means of a coil surrounding the vacuum vessel and supplied withhigh frequency energy.
- the magnesium is evaporated oil and most or all of the other impurities are thrown out of the molten mass in the crucible. 1
- the ingot of purified beryllium thus formed is melted by high frequency currentsa second time and this operation is again carried on with metal out of contact with a reactive atmosphere and melting the metal in a vacuum, contains films which appear to be made of an impurity. Those films form the surfaces of failure when hot rolling is attempted and seem to separate masses of metal, which would otherwise be workable while hot. As each individual lump of beryllium is covered with an exceedingly thin surface film of oxide, it seems probable that, when the lumps are melted preliminary to the formation of an ingot,
- the films of beryllium oxide become trapped within the latter and that the films found within the ingots are made of beryllium oxide.
- the difilculties arising from the presence of the films are overcome by adding to the beryllium prior to the melting thereof a small quantity of an agent which is capable of rendering the impurity ineffective to embrittle the beryllium.
- Titanium is an example of an agent that may be employed for the purpose and when a small quantity of that metal is melted with beryllium, there occurs a reaction evidenced by the evolution of considerable heat.
- the resulting material is substantially free of films and, although it is brittle in the cold state. it may be readily worked at moderately elevated temperatures.
- the starting material is a commercial grade of beryllium available on the market in the form of lumps about an inch or so in diameter. This material contains some slag inclusions and a considerable percentage of magnesium. Also there are other impurities, for example, aluminum, iron, and calcium, present in very much smaller amounts.
- the beryllium is first formed into an ingot and, for this purpose, the lumps,of the metal are placedwithin a crucible of beryllium oxide and melted out. of contact with areactive atmospreferably under high vacuum.
- a beryllium oxide mold of the self-pouring type is preferred and such a mold is somewhat similar to a funnel in that the main body thereof is of generally cylindrical section and its upper portion is of considerably larger diameter. The beryllium is placed in the upper portion of the mold and, when melted, runs down into the cylindrical portion, the I shape of the'mold eliminating piping.
- a small quantity of the agent which is to render harmless the impurity in the beryllium is added to the material to be remelted and the agent may be in the form of small granules which should be placed somewhere in the mold where they will come in contact with the beryllium. Thus, the granules may be placed within cavities in the beryllium ingot itself.
- the amount of the agent employed should not be less than about A;% and should not exceed 2% by weight of the beryllium, and when titanium is used, the best results are obtained when the amount of titanium varies from 34% to by weight of the beryllium. When present in such small percentages in the liquid alloy, the titanium is soluble near the melting point of beryllium.
- the beryllium and titanium are heated, an exothermic reaction occurs and the reaction starts before actual melting of the beryllium takes place and continues for some time, during which the metals are melted and flow down into the cylindrical portion of the mold.
- the titaniing the embrittling films and renders the impurity harmless.
- the titanium On the assumption that the films are formed of beryllium oxide, the titanium apparently reduces that compound within the melt to beryllium with the probable resultant formation of an oxide of titanium and the possible formation of unusual compounds, such as substantially free of films.
- the titanium does not appear to attack the beryllium oxide crucible but seems to have a selective action on the impurities present in the molten beryllium metal.
- the observed fact is that the films disappear from the lower portion of the ingot, leaving it homogeneous in structure and relatively bright on its surface, whereas the upper part of the ingot contains an oxide surface film giving it a somewhat tarnished appearance. If an excessive amount of titanium is used, the ingot does not have desirable working properties and it is, therefore, evident that the amount of titanium to be employed is that which will be suflicient to react with the impurity that is present within the ingot and little, if any, more than that amount.
- the alloy high in beryllium produced by the method above described has all of the desirable properties of pure beryllium and, in addition, is workable at temperatures below red heat and oi the order of 500 C.
- the material maybe rolled by successive passes into thin sheets less than .005" in thickness and vacuum-tight so that they may be used as X-ray windows, and, in addition, the material may behot forged into curved plates and drawn into cups.
- zirconium may be used instead of using titanium as the agent which reacts with the impurity which would otherwise embrittle the beryllium. Its action appears to be the same as that of the titanium and correspondingly small quantities may be employed to obtain the desired result.
- An alloy which consists of beryllium in excess of 98%, a trace of oxygen, and the remainder of a member taken from the class made up of titanium and zirconium which has chemically combined with at least a part of the oxygen.
- An alloy which consists of in excess of 98% I beryllium, from to less than 2% of a member of the class made up of titanium andzirconium, and a trace of oxygen, at least part of the oxygen being chemically combined with said member of said class.
- An alloy which'consists of in excess of 98% of beryllium, from /4% to of a member of the class made up of titanium and zirconium, and a trace of oxygen, at least part of the oxygen being in chemical combination with said member of said class.
- An alloy which consists oi in excess of 98% beryllium, not to exceed 2% of titanium, and a trace of oxygen, at least part of the oxygen being in chemical combination with the titanium.
- An alloy which consists of in excess of 98% beryllium, from to not more than 2% of titanium, and-a trace of oxygen, at least part of the oxygen being chemlcallycombined with the titanium.
- An alloy which consists of in excess of 98% of beryllium, from to of titanium, and a trace of oxygen, at least part of the oxygen being in chemical combination with the titanium.
- An alloy which consists of in excess of 98% beryllium, from to not more than 2% or zirconium, and a trace of oxygen, at least part of the oxygen being chemically combined with the zirconium.
- An alloy which consists of in excess of 98% of beryllium, from to of zirconium, and a trace of oxygen, at least part of the oxygen being in chemical combination with, the zirconium.
- An alloy which consists of beryllium in excess oi 98%, traces of impurities, and from to 2% of a member-o1 the class made up or titanium and zirconium, the alloy having substantially the characteristics of beryllium except for having such malleability as to permit it to be hot worked.
- a rolled vacuum-tight sheet less than .005" thick made of a material consisting of more than 98% beryllium, from to 2% of a member of the class made up of titanium and zirconium, and traces of impurities.
- a vacuum-tight X-ray window comprising a thin rolled sheet of an alloy comprising beryllium in excess of 98%, and from to 2% of a member of the class made up of titanium and zirconium, the window, being substantially as pervious to X-rays as one made of beryllium.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Dec. 2 9, 1942 UNITED STATES PATENT. OFFICE BEBYLLIUM ALLOY Gerard E. Claussen, Springdale,
to Machlett Laboratories Incorp rated,
Conm, assignor Springdaie, Conn., a corporation of Connecticut No Drawing. Application Serial No. 400,5
August 12,1041,
1t Claims. (cl. -150) This invention relates to alloys of high beryllium content and is concerned more particularly with a novel alloy of the kind specified and sheets,
. beryllium has heretofore had only a limited application in the arts.
The present invention is directed to the provision of a novel alloy which has substantially the same desirable physical characteristics as beryllium, but is much more malleable and ductile so that under suitable conditions, it may be readily worked into forms suitable for practical use.
Theinvention is based upon the discovery that ingots of beryllium, even though produced by phere. Preferably, the melting is carried on under a high vacuum, of the order of 0.001 mm. of mercury, and by high frequency currents induced in the metal by means of a coil surrounding the vacuum vessel and supplied withhigh frequency energy. In the melting operation, the magnesium is evaporated oil and most or all of the other impurities are thrown out of the molten mass in the crucible. 1
The ingot of purified beryllium thus formed is melted by high frequency currentsa second time and this operation is again carried on with metal out of contact with a reactive atmosphere and melting the metal in a vacuum, contains films which appear to be made of an impurity. Those films form the surfaces of failure when hot rolling is attempted and seem to separate masses of metal, which would otherwise be workable while hot. As each individual lump of beryllium is covered with an exceedingly thin surface film of oxide, it seems probable that, when the lumps are melted preliminary to the formation of an ingot,
the films of beryllium oxide become trapped within the latter and that the films found within the ingots are made of beryllium oxide.
According to the inventio the difilculties arising from the presence of the films are overcome by adding to the beryllium prior to the melting thereof a small quantity of an agent which is capable of rendering the impurity ineffective to embrittle the beryllium. Titanium is an example of an agent that may be employed for the purpose and when a small quantity of that metal is melted with beryllium, there occurs a reaction evidenced by the evolution of considerable heat. The resulting material is substantially free of films and, although it is brittle in the cold state. it may be readily worked at moderately elevated temperatures.
In the production of the new product, the starting material is a commercial grade of beryllium available on the market in the form of lumps about an inch or so in diameter. This material contains some slag inclusions and a considerable percentage of magnesium. Also there are other impurities, for example, aluminum, iron, and calcium, present in very much smaller amounts. The beryllium is first formed into an ingot and, for this purpose, the lumps,of the metal are placedwithin a crucible of beryllium oxide and melted out. of contact with areactive atmospreferably under high vacuum. A beryllium oxide mold of the self-pouring type is preferred and such a mold is somewhat similar to a funnel in that the main body thereof is of generally cylindrical section and its upper portion is of considerably larger diameter. The beryllium is placed in the upper portion of the mold and, when melted, runs down into the cylindrical portion, the I shape of the'mold eliminating piping.
A small quantity of the agent which is to render harmless the impurity in the beryllium is added to the material to be remelted and the agent may be in the form of small granules which should be placed somewhere in the mold where they will come in contact with the beryllium. Thus, the granules may be placed within cavities in the beryllium ingot itself. The amount of the agent employed should not be less than about A;% and should not exceed 2% by weight of the beryllium, and when titanium is used, the best results are obtained when the amount of titanium varies from 34% to by weight of the beryllium. When present in such small percentages in the liquid alloy, the titanium is soluble near the melting point of beryllium. When the beryllium and titanium are heated, an exothermic reaction occurs and the reaction starts before actual melting of the beryllium takes place and continues for some time, during which the metals are melted and flow down into the cylindrical portion of the mold. In the reaction, the titaniing the embrittling films and renders the impurity harmless. On the assumption that the films are formed of beryllium oxide, the titanium apparently reduces that compound within the melt to beryllium with the probable resultant formation of an oxide of titanium and the possible formation of unusual compounds, such as substantially free of films. The titanium does not appear to attack the beryllium oxide crucible but seems to have a selective action on the impurities present in the molten beryllium metal. Whatever the action may be, the observed fact is that the films disappear from the lower portion of the ingot, leaving it homogeneous in structure and relatively bright on its surface, whereas the upper part of the ingot contains an oxide surface film giving it a somewhat tarnished appearance. If an excessive amount of titanium is used, the ingot does not have desirable working properties and it is, therefore, evident that the amount of titanium to be employed is that which will be suflicient to react with the impurity that is present within the ingot and little, if any, more than that amount.
The alloy high in beryllium produced by the method above described has all of the desirable properties of pure beryllium and, in addition, is workable at temperatures below red heat and oi the order of 500 C. The material maybe rolled by successive passes into thin sheets less than .005" in thickness and vacuum-tight so that they may be used as X-ray windows, and, in addition, the material may behot forged into curved plates and drawn into cups.
In working the material, it is'preierably protected against strong oxidation and, for this purpose, a ortion of the lower part of the ingot produced in the second melt is removed and placed between protective sheets which may be of nickel or stainless steel, for example. These sheets are preferably crimped along the edges so that the piece of beryllium alloy between them -is substantially out of contact with the air. The
sheets with the piece of alloy between them are then raised to the desired temperature and subjected to the desired working operations.
Instead of using titanium as the agent which reacts with the impurity which would otherwise embrittle the beryllium, zirconium may be used. Its action appears to be the same as that of the titanium and correspondingly small quantities may be employed to obtain the desired result.
In the foregoing, I have described the melting operations as being carried on with the metals out ofcontact with a reactive atmosphere. Melt ing under. vacuum is perhaps the most convenient method of thus protecting the metals against oxidation but other expedients may be used, such as use of a protective atmosphere or possibly of I claim:
1. An alloy which consists of beryllium in excess of 98%, a trace of oxygen, and the remainder of a member taken from the class made up of titanium and zirconium which has chemically combined with at least a part of the oxygen.
2. An alloy which consists of in excess of 98% I beryllium, from to less than 2% of a member of the class made up of titanium andzirconium, and a trace of oxygen, at least part of the oxygen being chemically combined with said member of said class.
3. An alloy which'consists of in excess of 98% of beryllium, from /4% to of a member of the class made up of titanium and zirconium, and a trace of oxygen, at least part of the oxygen being in chemical combination with said member of said class.
, 4. An alloy which consists oi in excess of 98% beryllium, not to exceed 2% of titanium, and a trace of oxygen, at least part of the oxygen being in chemical combination with the titanium.
5. An alloy which consists of in excess of 98% beryllium, from to not more than 2% of titanium, and-a trace of oxygen, at least part of the oxygen being chemlcallycombined with the titanium.
6. An alloy which consists of in excess of 98% of beryllium, from to of titanium, and a trace of oxygen, at least part of the oxygen being in chemical combination with the titanium.
7. An alloy which consists of in excess of 98% beryllium, not to exceed 2% of zirconium, and a trace of oxygen, at least part of the oxygen being in chemical combination with the zirconium.
8. An alloy which consists of in excess of 98% beryllium, from to not more than 2% or zirconium, and a trace of oxygen, at least part of the oxygen being chemically combined with the zirconium.
9. An alloy which consists of in excess of 98% of beryllium, from to of zirconium, and a trace of oxygen, at least part of the oxygen being in chemical combination with, the zirconium.
10. An alloy which consists of beryllium in excess oi 98%, traces of impurities, and from to 2% of a member-o1 the class made up or titanium and zirconium, the alloy having substantially the characteristics of beryllium except for having such malleability as to permit it to be hot worked.
11. An alloy which consists of beryllium in excess of 98%, traces of impurities, and from to /2% of a member 01' the class made up of titanium and zirconium, the alloyhaving substantially the characteristics of beryllium except for having such malleability as to permit it to be hot worked. i
12. A rolled vacuum-tight sheet of a material consisting of more than 98% beryllium, from to 2% of a member or the class made up of titan-. ium and zirconium, and traces oi impurities;
13. A rolled vacuum-tight sheet less than .005" thick made of a material consisting of more than 98% beryllium, from to 2% of a member of the class made up of titanium and zirconium, and traces of impurities.
14. A vacuum-tight X-ray window comprising a thin rolled sheet of an alloy comprising beryllium in excess of 98%, and from to 2% of a member of the class made up of titanium and zirconium, the window, being substantially as pervious to X-rays as one made of beryllium. 15. An alloy containing from about to about 2% of a member of the class made up of titanium and zirconium, substantially the balance of the alloy being beryllium, said alloy being substantially as. permeable to X-rays as beryllium and having its malleability increased by the member of said class to a; suflicient extent to render Y the alloy hot workable.
- lium and having its malleability increased by the member of said class to a sufllcient. extent to render the alloy hot workable.
GERARD E.- CLAUSSEN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US406532A US2306592A (en) | 1941-08-12 | 1941-08-12 | Beryllium alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US406532A US2306592A (en) | 1941-08-12 | 1941-08-12 | Beryllium alloy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2306592A true US2306592A (en) | 1942-12-29 |
Family
ID=23608380
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US406532A Expired - Lifetime US2306592A (en) | 1941-08-12 | 1941-08-12 | Beryllium alloy |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2306592A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3145098A (en) * | 1961-06-27 | 1964-08-18 | Ass Elect Ind | Beryllium alloys |
| DE1188295B (en) * | 1961-03-08 | 1965-03-04 | Ass Elect Ind | Use of beryllium alloys |
-
1941
- 1941-08-12 US US406532A patent/US2306592A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1188295B (en) * | 1961-03-08 | 1965-03-04 | Ass Elect Ind | Use of beryllium alloys |
| US3145098A (en) * | 1961-06-27 | 1964-08-18 | Ass Elect Ind | Beryllium alloys |
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