US2775514A - Pyrophoric composition - Google Patents
Pyrophoric composition Download PDFInfo
- Publication number
- US2775514A US2775514A US344903A US34490353A US2775514A US 2775514 A US2775514 A US 2775514A US 344903 A US344903 A US 344903A US 34490353 A US34490353 A US 34490353A US 2775514 A US2775514 A US 2775514A
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- titanium
- zirconium
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- finely divided
- mixture
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06C—DETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
- C06C15/00—Pyrophoric compositions; Flints
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S149/00—Explosive and thermic compositions or charges
- Y10S149/11—Particle size of a component
- Y10S149/114—Inorganic fuel
Definitions
- This invention relates to pyrophoric compositions suitable for fuses and starting mixtures for bombs and general explosive materials.
- metallic titanium powder and metallic zirconium powder, or mixtures thereof have been found to be effective as fuse or starting mixtures without the limitations characteristic of the magnesium-type mixtures.
- Metallic titanium powder-type fuse mixtures in particular appear to be stable indefinitely under any of the types of climatic conditions to which a bomb may normally be subjected. These titanium-type starting mixtures cannot, however, be subjected to extreme pressure.
- titanium and zirconium powders in addition to being expensive, are dangerous to prepare and their degree of instability during preparation is such that serious losses are encountered due to premature ignition.
- titanium and zirconium alloys when physically admixed with such elements as sulfur, selenium, or tellurium, form an extremely active pyrophoric composition which is equal or superior in activity to powdered titanium, although these alloys alone in powdered form are substantially ineffective as a pyrophoric material.
- the pyrophoric mixtures of my invention are stable to a greater extent than titanium or zirconium metal powders when exposed to the types of conditions listed hereinbefore. Of still more importance, however, is the fact that when 7 2,715,514 Patented Dec. 25, 1956 these titanium and zirconium alloys are combined with sulfur, selenium or tellurium, they may be subjected to high compressive pressure without losing their effectivemess.
- the titanium and zirconium alloys which form such effective pyrophoric mixtures with sulfur, selenium and tellurium comprise alloys of titanium or zirconium, or both, with aluminum.
- the most useful range of compositions comprises alloys containing between 50 and by weight of titanium or zirconium, or both, and the balance essentially aluminum.
- the zirconium base alloys are more eifective than the titanium base alloys in the mixtures of my invention, and this increase in activity progresses with the zirconium content of the alloys from the level of the titanium base alloy up to the level of the zirconium base alloy. Regardless of their variation in titanium or zirconium content, the alloys may further contain from 2% to 10% by weight of either tin or silicon, or both.
- the aforementioned titanium and zirconium base alloys must contain from 10% to 30% by weight of aluminum in order to impart to a mixture of the alloy with sulphur, selenium or tellurium the stability referred to hereinbefore.
- the balance of the alloy will be composed of either tin or silicon, or both.
- Silicon in these alloys somewhat increases the pyrophoric effectiveness of the mixtures of my invention, but its primary advantage in the alloys is to increase their brittleness and thereby facilitate grinding of the alloys to powder form.
- Tin also somewhat increases the pyrophoric activity of the mixtures of my invention, but its presence is generally accounted for because it results from the advantageous use of tin or tin oxideduring alumino-thermic production of the base alloy.
- the aforementioned alloys may be prepared by sim ple fusion of their constituents, or by sintering in a nonoxidizing atmosphere the powders of the metal constituents of the desired alloy at conventional sintering temperatures for these metals, or the alloys may be prepared by reduction of alkali metal double fluorides or any or all of the metals titanium, zirconium, tin and silicon with .molten aluminum.
- the yield of metal from the oxidic component of the alumino-thermic mixture may be doubled by the inclusion in the mixture of sufiicient metallic tin or tin oxide to leave in the resulting alloy from 2% to 10% by weight of tin.
- the titanium or zirconium alloys used in the practice of my invention are initially made in the form of massive pigs which are then crushed to roughly inch in size.
- the crushed alloy is subsequently ground under water, for example, in an open end or vented ball mill using iron, balls, to a particle size at least fine enough so that the material will pass through a -325 mesh screen (Tyler Standard). Grinding to 400-600 mesh further increases the pyrophoric activity of the final mixture, and this range of particle size is therefore preferred for many purposes.
- the water is then drained from the ground alloy and the resulting powder is dried in air, advantageously at C.
- the powdered alloy is then mixed with sulfur, selenium, or tellurium, also in powder form, but because of its availability and cost, sulfur is preferred.
- the amount of sulfur (or other equivalent agent as aforementioned) which is used for this purpose may range from 2 to 50% by weight of the titanium or zirconium-containing alloy, the higher the content of sul fur the more violent the pyrophoricity of the resulting 3 mixture. lent) results in mixtures of increasing pyrophoricity when the alloys used in making these mixtures contain increasing proportions of zirconium as described hereinbefore.
- a range of sulfur (or its equivalent) from to 25% is preferred for a practical combination of effectiveness and economy.
- Mixing of the alloy and sulfur is advantageously carried out in a conventional double cone blender so that the powder is subject to as little attrition as possible.
- a pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the balance essentially aluminum, and (2) from 2 to 50% by weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
- a pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the balance essentially aluminum, and (2) from 5 to 25 by Weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
- a pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium, 2 to 10% each of at least one metal of the group consisting of silicon and tin, and the balance essentially aluminum, and (2) from 2 to 50% by weight of
- An pyrophoric composition which comprises a mix? ture of (1) a finely divided alloy composed essentially of 50 to of at least one of the metals of the group consisting of titanium and zirconium, 2 to 10% of tin, and the balance essentially aluminum, and. (2) from 2 to 50% by weight of Arms divided element of the group consisting of sulfur, selenium and tellurium.
- a pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the, group, con sisting of titanium. and zirconium and the balance es: sentially aluminum in the amount of 10 to. 30%, and (2) from 2 to 50% by weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
- a pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the balance essentially, aluminum, and (2) from 2 to 50% by weightof a finely divided element of the group consisting of sulfur, selenium g and tellurium, the finely divided components of the mixture having a particle size of minus 325 mesh.
- a pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium. and zirconium and the balance es sentially aluminum, and (2) from 2 to 50%-by weight of a finely divided element of the group consisting of sulfur,
- the finely divided components of the mixture having a particle size within the range of 400- 600.mesh.
- a pyrophoric composition which comprises. a compressed mixture of (l), a finely divided alloy composed es-. sentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the bal-.
- anee essentially aluminum and (2) from 2 to 50% by weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
Description
PYROPHORIC COIVIPOSIT ION Eugene Wainer, Cleveland Heights, Ohio, assignor to Horizons Incorporated, Princeton, N. J., a corporation of New Jersey No Drawing. Application March 26, 1953, Serial No. 344,903
11 Claims. (Cl. 52-2) This invention relates to pyrophoric compositions suitable for fuses and starting mixtures for bombs and general explosive materials.
The design of fire bombs and explosive bombs frequently involves a complicated combination of devices to insure proper operation of the bombs. Some of these designs require a three-part system consisting of a primer or primary ignition source, such as fulminate of mercury or an azide'compound. This ignited primer then initiates the combustion of a fuse mixture, and the ignition of this fuse mixture in turn establishes the proper combustion or explosive conditions for the main body of the bomb.
An important requirement of the aforementioned fuse or starting mixtures is stability during storage. They must be capable of being stored for long periods, frequently for years, under conditions of extreme cold or extreme heat, in very dry atmospheres or in exceptionally humid atmospheres. In spite of the rigors of such exposure, the fuse mixture should maintain all of its desirable combustion characteristics. Until recent years, an important ingredient of such fuse mixtures was magnesium metal powder or mixtures of magnesium and aluminum. However, an unfortunate property of the magnesium-type fuse mixtures is their relatively poor resistance to the aforementioned external storage conditions. For example, when stored in a very humid atmosphere, a magnesium fuse mixture loses all of its efiectiveness in a matter of a few months and the bomb incorporating this fuse will be a dud unless the fuse mixture is replaced. The magnesium fuse mixtures suifer from still another limitation in that they cannot be compressed and therefore must be used in a relatively loose open form.
In recent years, metallic titanium powder and metallic zirconium powder, or mixtures thereof, have been found to be effective as fuse or starting mixtures without the limitations characteristic of the magnesium-type mixtures. Metallic titanium powder-type fuse mixtures in particular appear to be stable indefinitely under any of the types of climatic conditions to which a bomb may normally be subjected. These titanium-type starting mixtures cannot, however, be subjected to extreme pressure. Moreover, titanium and zirconium powders, in addition to being expensive, are dangerous to prepare and their degree of instability during preparation is such that serious losses are encountered due to premature ignition.
I have now discovered that certain titanium and zirconium alloys, when physically admixed with such elements as sulfur, selenium, or tellurium, form an extremely active pyrophoric composition which is equal or superior in activity to powdered titanium, although these alloys alone in powdered form are substantially ineffective as a pyrophoric material. Moreover, the pyrophoric mixtures of my invention are stable to a greater extent than titanium or zirconium metal powders when exposed to the types of conditions listed hereinbefore. Of still more importance, however, is the fact that when 7 2,715,514 Patented Dec. 25, 1956 these titanium and zirconium alloys are combined with sulfur, selenium or tellurium, they may be subjected to high compressive pressure without losing their effectivemess.
The titanium and zirconium alloys which form such effective pyrophoric mixtures with sulfur, selenium and tellurium comprise alloys of titanium or zirconium, or both, with aluminum. In general, the most useful range of compositions comprises alloys containing between 50 and by weight of titanium or zirconium, or both, and the balance essentially aluminum. The zirconium base alloys are more eifective than the titanium base alloys in the mixtures of my invention, and this increase in activity progresses with the zirconium content of the alloys from the level of the titanium base alloy up to the level of the zirconium base alloy. Regardless of their variation in titanium or zirconium content, the alloys may further contain from 2% to 10% by weight of either tin or silicon, or both.
The aforementioned titanium and zirconium base alloys must contain from 10% to 30% by weight of aluminum in order to impart to a mixture of the alloy with sulphur, selenium or tellurium the stability referred to hereinbefore. In such alloys wherein the total content of titanium or zirconium, or both, plus aluminum is less than 100%, the balance of the alloy will be composed of either tin or silicon, or both. Silicon in these alloys somewhat increases the pyrophoric effectiveness of the mixtures of my invention, but its primary advantage in the alloys is to increase their brittleness and thereby facilitate grinding of the alloys to powder form. Tin also somewhat increases the pyrophoric activity of the mixtures of my invention, but its presence is generally accounted for because it results from the advantageous use of tin or tin oxideduring alumino-thermic production of the base alloy.
The aforementioned alloys may be prepared by sim ple fusion of their constituents, or by sintering in a nonoxidizing atmosphere the powders of the metal constituents of the desired alloy at conventional sintering temperatures for these metals, or the alloys may be prepared by reduction of alkali metal double fluorides or any or all of the metals titanium, zirconium, tin and silicon with .molten aluminum. However, I presently prefer, for economical reasons, to prepare the alloys in massive form by conventional alumino-thermic technique. When the alloy is produced by such alurnino-thermic procedure, the yield of metal from the oxidic component of the alumino-thermic mixture may be doubled by the inclusion in the mixture of sufiicient metallic tin or tin oxide to leave in the resulting alloy from 2% to 10% by weight of tin.
' The titanium or zirconium alloys used in the practice of my invention are initially made in the form of massive pigs which are then crushed to roughly inch in size. The crushed alloy is subsequently ground under water, for example, in an open end or vented ball mill using iron, balls, to a particle size at least fine enough so that the material will pass through a -325 mesh screen (Tyler Standard). Grinding to 400-600 mesh further increases the pyrophoric activity of the final mixture, and this range of particle size is therefore preferred for many purposes. The water is then drained from the ground alloy and the resulting powder is dried in air, advantageously at C. The powdered alloy is then mixed with sulfur, selenium, or tellurium, also in powder form, but because of its availability and cost, sulfur is preferred. The amount of sulfur (or other equivalent agent as aforementioned) which is used for this purpose may range from 2 to 50% by weight of the titanium or zirconium-containing alloy, the higher the content of sul fur the more violent the pyrophoricity of the resulting 3 mixture. lent) results in mixtures of increasing pyrophoricity when the alloys used in making these mixtures contain increasing proportions of zirconium as described hereinbefore. A range of sulfur (or its equivalent) from to 25% is preferred for a practical combination of effectiveness and economy. Mixing of the alloy and sulfur is advantageously carried out in a conventional double cone blender so that the powder is subject to as little attrition as possible.
The effectiveness of the mixtures of the present invention, compared with that of a mixture of titanium metal powder and sulfur such as that described in United States Patent No. 2,461,544, can be appreciated by a comparison of their ignition activities. These activities are indicated in the following table by the time required for each mixture to burn when packed in the form of a minus 325 mesh powder in a combustion tube having an inside diameter of 0.25 inch and a length of inches:
2 Al percent percent percent Si, percent Burning Time Sample percent It will be seen that the mixtures of my invention, as represented in the foregoing table, are actively pyrophoric and that their degree of activity in this respect can be readily controlled by proportioning their constituents as previously described. All of these mixtures are furthermore stable with respect to ambient storage atmospheric conditions as well as with respect to their safe use, and they are moreover capable of being compressed (the physical condition generally preferred for fuse and starting mixtures) without danger of their premature ignition.
I claim:
1. A pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the balance essentially aluminum, and (2) from 2 to 50% by weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
2. A pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the balance essentially aluminum, and (2) from 5 to 25 by Weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
3. A pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium, 2 to 10% each of at least one metal of the group consisting of silicon and tin, and the balance essentially aluminum, and (2) from 2 to 50% by weight of afinely divided element of Any specific amount of sulfur (or its equiva- 5. A pyrophoric composition which comprises a mix? ture of (1) a finely divided alloy composed essentially of 50 to of at least one of the metals of the group consisting of titanium and zirconium, 2 to 10% of tin, and the balance essentially aluminum, and. (2) from 2 to 50% by weight of afinely divided element of the group consisting of sulfur, selenium and tellurium.
6. A pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the, group, con sisting of titanium. and zirconium and the balance es: sentially aluminum in the amount of 10 to. 30%, and (2) from 2 to 50% by weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
of 1) a finely divided alloy composed essentially of 50 to 80% of zirconium and the balance essentially.
aluminum, and (2) from 2 to 50% by weight of a. finely divided element of the group consisting of sulfur, selenium and tellurium.
9. A pyrophoric composition which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the balance essentially, aluminum, and (2) from 2 to 50% by weightof a finely divided element of the group consisting of sulfur, selenium g and tellurium, the finely divided components of the mixture having a particle size of minus 325 mesh.
10. A pyrophoric composition: which comprises a mixture of (1) a finely divided alloy composed essentially of 50 to 80% of at least one of the metals of the group consisting of titanium. and zirconium and the balance es sentially aluminum, and (2) from 2 to 50%-by weight of a finely divided element of the group consisting of sulfur,
selenium andtellurium, the finely divided components of the mixture having a particle size within the range of 400- 600.mesh.
11. A pyrophoric composition which comprises. a compressed mixture of (l), a finely divided alloy composed es-. sentially of 50 to 80% of at least one of the metals of the group consisting of titanium and zirconium and the bal-. A
anee essentially aluminum, and (2) from 2 to 50% by weight of a finely divided element of the group consisting of sulfur, selenium and tellurium.
References Citedin the file of this patent UNITED STATES. PATENTS 2,272,779 Sarbey Feb. 10, 1942 2,370,159 Hanl'ey Feb. 27, 1945 1 2,450,892 Hale Oct. 12, 1948 2,461,544 Hale et a1 Feb. 15, 1949 2,467,334 Hale et a1. Apr. 12, 1949'
Claims (2)
1. A PYROPHORIC COMPOSITION WHICH COMPRISES A MIXTURE OF (1) A FINELY DIVIDED ALLOY COMPOSED ESSENTIALLY OF 50 TO 80% OF AT LEAST ONE OF THE METALS OF THE GROUP CONSISTING OF TITANIUM AND ZIRCONIUM AND THE BALANCE ESSENTIALLY ALUMINUM, AND (2) FROM 2 TO 20% BY WEIGHT OF A FINELY DIVIDED ELEMENT OF THE GROUP CONSISTING OF SULFUR, SELENIUM AND TELLURIUM.
3. A PYROPHORIC COMPOSITION WHICH COMPRISES A MIXTURE OF (1) A FINELY DIVIDED ALLOY COMPOSED ESSENTIALLY OF 50 TO 80% OF AT LEAST ONE OF THE METALS OF THE GROUP CONSISTING OF TITANIUM AND ZIRCONIUM, 2 TO 10% EACH OF AT LEAST ONE METAL OF THE GROUP CONSISTING OF SILICON AND TIN, AND THE BALANCE ESSENTIALLY ALUMINUM, AND (2) FROM 2 TO 50% BY WEIGHT OF A FINELY DIVIDED ELEMENT OF THE GROUP CONSISTING OF SULFUR, SELENIUM AND TELLURIUM.
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US344903A US2775514A (en) | 1953-03-26 | 1953-03-26 | Pyrophoric composition |
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US344903A US2775514A (en) | 1953-03-26 | 1953-03-26 | Pyrophoric composition |
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US2775514A true US2775514A (en) | 1956-12-25 |
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2887370A (en) * | 1957-02-12 | 1959-05-19 | Reed E Donnard | Non-corrosive percussion primer material |
US2951752A (en) * | 1958-05-21 | 1960-09-06 | Stevenson Thomas | Incendiary composition |
US3028808A (en) * | 1958-01-09 | 1962-04-10 | Samuel J Porter | Armor piercing incendiary projectile |
US3053708A (en) * | 1959-02-12 | 1962-09-11 | Phillips Petroleum Co | High impulse solid propellant composition |
US3118799A (en) * | 1961-10-24 | 1964-01-21 | Atlas Chem Ind | Delay compositions for delay electric detonators |
US3396060A (en) * | 1960-11-02 | 1968-08-06 | Army Usa | Incendiary composition consisting of titanium, aluminum-magnesium alloy, and inorganic oxidizer salt |
US4112846A (en) * | 1965-06-11 | 1978-09-12 | Martin Marietta Aluminum Inc. | Armor-piercing incendiary projectile |
FR2453840A1 (en) * | 1979-04-11 | 1980-11-07 | Fraga Dominguez Ramon | Lighter flint prodn. - by compacting a suitable powder mixt. sintering extruding and cutting to size |
US4402776A (en) * | 1980-08-22 | 1983-09-06 | Hughes Aircraft Company | Silicon-containing compositions for self-sustained intermetallic reactions |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2272779A (en) * | 1939-12-27 | 1942-02-10 | Hartford Nat Bank & Trust Co | Flash lamp |
US2370159A (en) * | 1942-07-03 | 1945-02-27 | Hercules Powder Co Ltd | Electric squib |
US2450892A (en) * | 1944-05-05 | 1948-10-12 | George C Hale | Delay powder |
US2461544A (en) * | 1944-06-09 | 1949-02-15 | George C Hale | Fuse powder composition |
US2467334A (en) * | 1944-07-05 | 1949-04-12 | George C Hale | Fuse powder composition |
-
1953
- 1953-03-26 US US344903A patent/US2775514A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2272779A (en) * | 1939-12-27 | 1942-02-10 | Hartford Nat Bank & Trust Co | Flash lamp |
US2370159A (en) * | 1942-07-03 | 1945-02-27 | Hercules Powder Co Ltd | Electric squib |
US2450892A (en) * | 1944-05-05 | 1948-10-12 | George C Hale | Delay powder |
US2461544A (en) * | 1944-06-09 | 1949-02-15 | George C Hale | Fuse powder composition |
US2467334A (en) * | 1944-07-05 | 1949-04-12 | George C Hale | Fuse powder composition |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2887370A (en) * | 1957-02-12 | 1959-05-19 | Reed E Donnard | Non-corrosive percussion primer material |
US3028808A (en) * | 1958-01-09 | 1962-04-10 | Samuel J Porter | Armor piercing incendiary projectile |
US2951752A (en) * | 1958-05-21 | 1960-09-06 | Stevenson Thomas | Incendiary composition |
US3053708A (en) * | 1959-02-12 | 1962-09-11 | Phillips Petroleum Co | High impulse solid propellant composition |
US3396060A (en) * | 1960-11-02 | 1968-08-06 | Army Usa | Incendiary composition consisting of titanium, aluminum-magnesium alloy, and inorganic oxidizer salt |
US3118799A (en) * | 1961-10-24 | 1964-01-21 | Atlas Chem Ind | Delay compositions for delay electric detonators |
US4112846A (en) * | 1965-06-11 | 1978-09-12 | Martin Marietta Aluminum Inc. | Armor-piercing incendiary projectile |
FR2453840A1 (en) * | 1979-04-11 | 1980-11-07 | Fraga Dominguez Ramon | Lighter flint prodn. - by compacting a suitable powder mixt. sintering extruding and cutting to size |
US4402776A (en) * | 1980-08-22 | 1983-09-06 | Hughes Aircraft Company | Silicon-containing compositions for self-sustained intermetallic reactions |
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