US1650631A - Process of preparing metals with high-temperature fusing points such as tungsten andof preparing wire therefrom - Google Patents
Process of preparing metals with high-temperature fusing points such as tungsten andof preparing wire therefrom Download PDFInfo
- Publication number
- US1650631A US1650631A US611156A US61115623A US1650631A US 1650631 A US1650631 A US 1650631A US 611156 A US611156 A US 611156A US 61115623 A US61115623 A US 61115623A US 1650631 A US1650631 A US 1650631A
- Authority
- US
- United States
- Prior art keywords
- tungsten
- preparing
- crystal
- andof
- metals
- 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
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- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 title description 29
- 229910052721 tungsten Inorganic materials 0.000 title description 18
- 239000010937 tungsten Substances 0.000 title description 18
- 238000000034 method Methods 0.000 title description 11
- 229910052751 metal Inorganic materials 0.000 title description 10
- 239000002184 metal Substances 0.000 title description 10
- 150000002739 metals Chemical class 0.000 title description 3
- 239000013078 crystal Substances 0.000 description 40
- 238000004519 manufacturing process Methods 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- 238000005245 sintering Methods 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 235000011149 sulphuric acid Nutrition 0.000 description 4
- 239000001117 sulphuric acid Substances 0.000 description 4
- 238000005530 etching Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 241000370685 Arge Species 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- XAYGUHUYDMLJJV-UHFFFAOYSA-Z decaazanium;dioxido(dioxo)tungsten;hydron;trioxotungsten Chemical compound [H+].[H+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].[NH4+].O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O.[O-][W]([O-])(=O)=O XAYGUHUYDMLJJV-UHFFFAOYSA-Z 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002927 oxygen compounds Chemical class 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- CMPGARWFYBADJI-UHFFFAOYSA-L tungstic acid Chemical compound O[W](O)(=O)=O CMPGARWFYBADJI-UHFFFAOYSA-L 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01K—ELECTRIC INCANDESCENT LAMPS
- H01K3/00—Apparatus or processes adapted to the manufacture, installing, removal, or maintenance of incandescent lamps or parts thereof
- H01K3/02—Manufacture of incandescent bodies
Definitions
- the wire has been made from tungsten, for example, as follows: A bar of pressed tungsten powder is heated to a lllgl'l temperature until the powder is sintered into a body which consists of crystals more or less closely joined. This bar-like body is then subjected to the well-known hammering and drawing process at high temperatures and thereby transformed gradually from the brittle condition, which is the condition of the bar, to a ductile wire, that is,
- the sizes of the small grains of the crystalline bar cannot always be exactly controlled so that in practice the individual char es of metal give bars having grains of di erent sizes and even with the most uniform progress of mechanical working the wires are not exactly alike.
- the tungsten bars are converted into a single crystal or into a few crystals.
- the properties of such a macro-crystal are always the same and are not subject to any chance variations.
- the macro-crystal is to be recognized from the fact that in case of weak etching it shows large uniformly reflecting surfaces and not surfaces which reflect differently from place to place; and further, in that it splits in accordance with natural cleavage planes and finally after strong etching it becomes angular in shape, even though round in the beginning.
- the process may be carried out by sintering preliminarily and thereafter highly sintering again bars pressed from powdered metal after which they are kept for a considerable time in a vacuum or in an indifierent or reducing gas atmosphere at temperatures near the melting point of the metal.
- the microscopic crystals of the powder become coarser, combining very gradually and almost uniformly until after a time which may be as much as several hours, a macroscopic crystal forms at one point which is much larger than all the others and which now absorbs its neighbors in a comparatively short timein a few minutes sometimes.
- the crystal may be thus increased to such an extent that finally the whole body may consist of a single crystal.
- the hydro gen used is preferably passed through sulphuric acid of a predetermined concentration. If the ingots of a given batch of tungsten metal are found to give about 8 to 10 crystals with well dried hydrogen from a given source, then if this same hydrogen is passed through 50% sulphuric acid, for example, the ingots from the same batch may be found to consist of only 3 to 5 crystals. If the moisture content is further increased, a single crystal results.
- Crystallized ammonium paratungstate is transformed by heating to a red glow into tungstic acid. This is reduced in a porcelain tube furnace b means of hydrogen at about 1,000 deg. to tungsten metal powder. This power is resse into ingots and the ingots are eated for about half an hour at 1300 deg.
- the b0 y reviously sintered in this manner is broug t to a temperature near the melting point or in'the neighborhood of 3000 C. in a very well dried stream of hydro en, by sending through it a low voltage a ternating current of high amperage. After'coolg, it can be determined by etching whether the desired crystallization has begun. This process of heating and checking up b etchmg is repeated until the body is trans ormed into one or more macro-crystals. If it consists of only one crystal, the remaining inots of this batch are heated for the same ength of time with hydrogen of the same degree of dryness.
- the hydrogen in the next ingot is passed through a washin bottle with sulphuric acid and is eated in the same man ner. If then, a body consisting of a single crystal is obtained, the work is continued in the same manner, otherwise, the concentration of the sulphuric acid will be varied until this result is reached.
- the method of making tungsten wire which consists in first making a large brittle tungsten crystal and then working this crystal into a flexible and'ductile state.
- the method of making tungsten wire which consists in compressing powdered tungsten, sintering it into a large crystal in an atmosphere of reducing gas which gas is provided beforehand with a proper proportion of oxygen compound and thereafter working the crystal into a flexible and ductile state.
- tungsten wire which consists in compressing powdered tungsten, sintering it into a large crystal in an atmosphere of reducing gas which gas is provided beforehand with a. proper proportion of water and thereafter working the crystal into a flexible and ductile state.
- tun sten wire which consists in first making a arge brittle tungsten crystal and then working the crystal while still hot into a flexible and ductile state.
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Powder Metallurgy (AREA)
Description
Patented Nov. 29, 1927.
UNITED STATES PATENT OFFICE.
IRITZ KOREF, OF CHARLOTTENBURG, AND HANS ALTERTHUM, OF HALENSEE, NEAR BERLIN, GERMANY, ASSIGNORS TO GENERAL ELECTRIC COMPANY, A CORPORA- TION OF NEW YORK.
PROCESS OF PREPARING METALS WITH HIGH-TEMPERATURE FUSING POINTS SUCH AS TUNGSTEN AND OF PREPARING WIRE THEREFROM.
No Drawing. Application filed January 6, 1923, Serial No. 611,156, and in Germany August 17, 1922.
metals.
Heretofore the wire has been made from tungsten, for example, as follows: A bar of pressed tungsten powder is heated to a lllgl'l temperature until the powder is sintered into a body which consists of crystals more or less closely joined. This bar-like body is then subjected to the well-known hammering and drawing process at high temperatures and thereby transformed gradually from the brittle condition, which is the condition of the bar, to a ductile wire, that is,
one which is flexible and adapted to be drawn cold.
The sizes of the small grains of the crystalline bar cannot always be exactly controlled so that in practice the individual char es of metal give bars having grains of di erent sizes and even with the most uniform progress of mechanical working the wires are not exactly alike.
Among the objects of our invention are the following: to overcome the foregoing objection; to prepare tungsten bars in the form of a single crystal or in the form of only a few crystals; to prepare tungsten wire from bars of the above form, to provide other details of improvement in processes of the above character, tending to increase their efliciency and serviceability.
To accomplish the foregoing and other useful ends our invention consists of details hereinafter more fully set forth and claimed.
In the contemplated process, the tungsten bars are converted into a single crystal or into a few crystals. The properties of such a macro-crystal are always the same and are not subject to any chance variations. The macro-crystal is to be recognized from the fact that in case of weak etching it shows large uniformly reflecting surfaces and not surfaces which reflect differently from place to place; and further, in that it splits in accordance with natural cleavage planes and finally after strong etching it becomes angular in shape, even though round in the beginning.
The process may be carried out by sintering preliminarily and thereafter highly sintering again bars pressed from powdered metal after which they are kept for a considerable time in a vacuum or in an indifierent or reducing gas atmosphere at temperatures near the melting point of the metal. As a result the microscopic crystals of the powder become coarser, combining very gradually and almost uniformly until after a time which may be as much as several hours, a macroscopic crystal forms at one point which is much larger than all the others and which now absorbs its neighbors in a comparatively short timein a few minutes sometimes. The crystal may be thus increased to such an extent that finally the whole body may consist of a single crystal. Sometimes it occurs that several such crystals are formed at diflerent points, each of which then continues to grow independently until it comes in contact with its neighbor or neighbors of the same order of magnitude with which, however, it does not combine. The body then consists of several large crystals and it is possible, by mechanical sub-division, for example, to take several different pieces, each of which consists of a single macrocrystal. The time which elapses before crystallization occurs may be shortened by increasing the temperature.
With respect to the number of crystals formed during the process, it is found that they differ in the case of different batches of metal made in regular operation, but in metal taken from any one batch, it is sub stantially constant.
It is found desirable to carry on the process in a reducing atmosphere and that then the number of crystals produced may be influenced by a certain small moisture content in the atmosphere. To this end, the hydro gen used is preferably passed through sulphuric acid of a predetermined concentration. If the ingots of a given batch of tungsten metal are found to give about 8 to 10 crystals with well dried hydrogen from a given source, then if this same hydrogen is passed through 50% sulphuric acid, for example, the ingots from the same batch may be found to consist of only 3 to 5 crystals. If the moisture content is further increased, a single crystal results. However, too great not have t -the crystalline tungsten) softened condition, sub ected to the usual process of mechanical working, wherein after the reduction in diameter amounting to about 20%, it loses its elasticity mentioned above. This may be recognized by the fact that a iece cut out with parallel sides in case oft e slow rise of pressure, can no longer be compressed cold by even a small amount without splitting. In the further course of hammering andi'drawing, the ductility gradually develo s just as in the case of wire in the wellown process which is drawn from a bar in a small crystalline state. In this ductile condition, the metal is suitable for use in incandescent lamps.
The following rule may be followed in making single crystal tungsten: Crystallized ammonium paratungstate is transformed by heating to a red glow into tungstic acid. This is reduced in a porcelain tube furnace b means of hydrogen at about 1,000 deg. to tungsten metal powder. This power is resse into ingots and the ingots are eated for about half an hour at 1300 deg.
C. in order to give them the cohesion necessa for the further treatment. Then the b0 y reviously sintered in this manner is broug t to a temperature near the melting point or in'the neighborhood of 3000 C. in a very well dried stream of hydro en, by sending through it a low voltage a ternating current of high amperage. After'coolg, it can be determined by etching whether the desired crystallization has begun. This process of heating and checking up b etchmg is repeated until the body is trans ormed into one or more macro-crystals. If it consists of only one crystal, the remaining inots of this batch are heated for the same ength of time with hydrogen of the same degree of dryness. If, on the contrary, it consists of 10 macro-crystals, for example, the hydrogen in the next ingot is passed through a washin bottle with sulphuric acid and is eated in the same man ner. If then, a body consisting of a single crystal is obtained, the work is continued in the same manner, otherwise, the concentration of the sulphuric acid will be varied until this result is reached.
What we claim as new, and desire to secure by Letters Patent of the United States, I
1. The method of making tungsten wire which consists in first making a large brittle tungsten crystal and then working this crystal into a flexible and'ductile state.
2. The method of making tungsten wire which consists in compressing powdered tungsten, sintering it into a large brittle crystal and thereafter working the crystal into a flexible and ductile state.
3. The method of making tungsten wire which consists in compressing powdered tungsten, sintering it into a large crystal in an atmosphere of reducing gas, and thereafter working the crystal into a flexible and ductile state.
4. The method of making tungsten wire which consists in compressing" powdered tungsten, sinterin it into a large crystal in an atmosphere 0 reducing gas one of the constituents of which is oxygen and thereafter working the crystal into a flexible and ductile state.
5. The method of making tungsten wire which consists in compressing powdered tungsten, sintering it into a large crystal in an atmosphere of reducing gas which gas is provided beforehand with a proper proportion of oxygen compound and thereafter working the crystal into a flexible and ductile state.
6. The method of making tungsten wire which consists in compressing powdered tungsten, sintering it into a large crystal in an atmosphere of reducing gas which gas is provided beforehand with a. proper proportion of water and thereafter working the crystal into a flexible and ductile state.
7. The method of making tun sten wire which consists in first making a arge brittle tungsten crystal and then working the crystal while still hot into a flexible and ductile state. i
8. The method of making tungsten wire which consists in compressing powdered tungsten, sintering it into a large crystal in an atmosphere of reducing gas, and thereafter wor in the crystal while still hot into a flexible an ductile state.
9. The method of making tungsten wire which is ductile cold, characterized by the feature that at first a large tungsten single crystal is made, and this is worked through a brittle stage by mechanical workin until it passes over into a state in which it is flexible and ductile when cold.
In witness whereof, we have hereunto set our hands this 9th day of December, 1922.
FRITZ KOREE. HANS ALTERTHUM.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1650631X | 1922-08-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1650631A true US1650631A (en) | 1927-11-29 |
Family
ID=7738257
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US611156A Expired - Lifetime US1650631A (en) | 1922-08-17 | 1923-01-06 | Process of preparing metals with high-temperature fusing points such as tungsten andof preparing wire therefrom |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1650631A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110209922A1 (en) * | 2009-06-05 | 2011-09-01 | Varel International | Casing end tool |
-
1923
- 1923-01-06 US US611156A patent/US1650631A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110209922A1 (en) * | 2009-06-05 | 2011-09-01 | Varel International | Casing end tool |
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