US3476623A - Metal azide electrically conductive priming composition and manufacture thereof - Google Patents

Metal azide electrically conductive priming composition and manufacture thereof Download PDF

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Publication number
US3476623A
US3476623A US719838A US3476623DA US3476623A US 3476623 A US3476623 A US 3476623A US 719838 A US719838 A US 719838A US 3476623D A US3476623D A US 3476623DA US 3476623 A US3476623 A US 3476623A
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United States
Prior art keywords
electrically conductive
azide
manufacture
priming composition
amount
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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US719838A
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English (en)
Inventor
Helmut Menke
Peter Roh
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dynamit Nobel AG
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Dynamit Nobel AG
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Publication date
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Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06CDETONATING OR PRIMING DEVICES; FUSES; CHEMICAL LIGHTERS; PYROPHORIC COMPOSITIONS
    • C06C7/00Non-electric detonators; Blasting caps; Primers
    • C06C7/02Manufacture; Packing

Definitions

  • the relation relates to a process for the manufacture of electrically conductive priming compositions for rapid acting gap detonators. More particularly this invention relates to the manufacture of electrically conductive compositions for rapid acting gap detonators which can be ignited within a few microseconds by very low energies.
  • Such detonators are increasingly needed by the art and particularly for piezoelectric detonators. They are supposed to be able to be ignited within a few microseconds and by means of very low energies (less than microwatt-seconds) Such detonators have been manufactured, for example, in the following manner. A priming composition is pressed into a narrow gap of a few microns in width, which forms a spark gap. The priming charge is ignited by a bridging spark.
  • an electrically conductive priming composition is pressed into a gap of narrow width.
  • a priming composition of this kind can be rapidly ignited utilizing low energies if it is based on a composition which is recognized by the art as appropriate for such purpose.
  • a number of methods are known for the preparation of electrically conducting priming compositions.
  • One process has been proposed wherein initiating exposives such as lead azide or silver azide are mixed with an amount of graphite. It is difiicult to prepare a homogeneous mixture from these materials.
  • initiating exposives such as lead azide or silver azide
  • graphite an amount of graphite
  • it is difiicult to prepare a homogeneous mixture from these materials.
  • a certain amount of time is required for the mixing itself and it has been established that a fairly long time is needed for the preparation of a homogeneous mixture of the foregoing components which, in this case, entails considerable danger.
  • the initiating charge becomes so friction sensitive and shock sensitive that detonation occurs during the mixing operation.
  • some hydrazine is added to the silver azide to reduce a part of the azide to silver, which then forms the conductive agent of the priming charge.
  • a small percentage of the azide is supposed to be reduced. It has been found, however, that a homogeneous mixture is not obtained by this method, and instead only small conductive foci are usually formed in the reduction.
  • the silver azide is reduced by ultraviolet radiation. This procedure has not proved satisfactory either because the upper strata are reduced considerably more than the underlying material, i.e., a homogeneous mixture is not obtained.
  • electrically conductive priming compositions for rapid acting gap detonators can be obtained without any of the above-mentioned disadvantages by mixing in a first step an electrical conducting agent with a secondary explosive and thereafter in a second stage mixing the mixture thus obtained with an initiating explosive.
  • a secondary explosive is meant a highly brisant explosive having a detonation speed of more than 5000 meters per second.
  • compositions in accordance with the invention can be ignited by means of very low energies and specifically with energies of less than 20 microwatt-seconds.
  • the induction period is characteristically very low, ignition taking place in less than 10 microseconds. This is particularly important as the priming compositions are often used in shaped charges.
  • Suitable secondary explosive include nitropentaerythritol, nitromannitol, hexogen and trinitrotoluene.
  • suitable electric conducting agents are, for example, graphite and colloidal silver.
  • the amount of electrically conducting agent present in the mixture varies with the resistance desired and the gap width of the detonation.
  • the resistance of the detonator may vary with 209 to 50,0000 depending on the intended application and preferably amounts to from about 2 to about 15 wt. percent. If the electrically conducting agent is graphite, the same is preferably used in amount of from 5 to 15 wt. percent referred to the total composition and if silver is used the same is preferably used in an amount of about 2 to 10 wt. percent.
  • the secondary explosive is required to be present in an amount of at least 10 wt. percent and is preferably present in an amount of more than 25 wt. percent referred to the total composition.
  • Example 1 55 parts by weight of nitropentaerythritol were mixed with 5 parts of graphite so as to produce a homogeneous mixture. The product thereby obtained was mixed with 40 parts of lead azide until a homogeneous mixture had again been formed. The mixture was then compacted by the conventional methods. The resulting mixture could be reliably ignited over a gap of 0.2 mm. width with an energy of 2 to 1.0 microwatt-seconds. The induction period of the ignition amounted to about 2-3 microseconds.
  • a charge which consisted of the above mixture had an extremely high detonation rate, required very little energy for ignition, and is extremely safe to handle both in manufacturing and processing.
  • Example 2 The procedure of Example 1 was repeated using 8% graphite, 32% nitromannitol and 60% lead azide. The resulting mixture could be readily ignited over a gapwidth of 0.2 mm. width with an energy of 10-15 microwatt-seconds. The induction period of the ignition amounted to about 5-7 microseconds.
  • Example 3 In accordance with the method of the invention, priming compositions are made available wherein the three critical components are present in the mixture in any desired ratios. However, for the realization of an adequate initiating effect the percentage of the initiating explosive must amount to at least 30%.
  • An electrically conductive priming composition for rapid acting gap detonators comprising an electrically conductive material selected from the group consisting of graphite, carbon black and colloidal silver, a secondary explosive selected from the group consisting of pe'ntaerythritol tetranitrate, mannitol, hexanitrate, cyclotrimethylenetrinitramine and trinitrotoluene and an initiating explosive selected from the group consisting of silve azide and lead azide.
  • An electrically conductive priming composition according to claim 1 consisting essentially of:
  • An electrically conductive priming composition according to claim 1 consisting essentially of:
  • An electrically conductive priming composition according to claim 1 consisting essentially of:
  • said electrically conducting agent is silver and is present in an amount of from 2 to 10 wt. percent referred to the total composition.

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Contacts (AREA)
  • Conductive Materials (AREA)
  • Powder Metallurgy (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US719838A 1967-04-13 1968-04-09 Metal azide electrically conductive priming composition and manufacture thereof Expired - Lifetime US3476623A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DED0052792 1967-04-13

Publications (1)

Publication Number Publication Date
US3476623A true US3476623A (en) 1969-11-04

Family

ID=7054453

Family Applications (1)

Application Number Title Priority Date Filing Date
US719838A Expired - Lifetime US3476623A (en) 1967-04-13 1968-04-09 Metal azide electrically conductive priming composition and manufacture thereof

Country Status (7)

Country Link
US (1) US3476623A (enrdf_load_stackoverflow)
BE (1) BE713570A (enrdf_load_stackoverflow)
CH (1) CH491060A (enrdf_load_stackoverflow)
FR (1) FR1562370A (enrdf_load_stackoverflow)
GB (1) GB1189952A (enrdf_load_stackoverflow)
IL (1) IL29794A (enrdf_load_stackoverflow)
NL (1) NL6805196A (enrdf_load_stackoverflow)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49100209A (enrdf_load_stackoverflow) * 1973-02-02 1974-09-21
US3873579A (en) * 1969-08-20 1975-03-25 Us Navy Organic azides and method of preparation thereof
JPS5082212A (enrdf_load_stackoverflow) * 1973-11-29 1975-07-03
US4428292A (en) 1982-11-05 1984-01-31 Halliburton Company High temperature exploding bridge wire detonator and explosive composition
US4696705A (en) * 1986-12-24 1987-09-29 Trw Automotive Products, Inc. Gas generating material
US4696231A (en) * 1986-02-25 1987-09-29 E. I. Du Pont De Nemours And Company Shock-resistant delay detonator
US4698107A (en) * 1986-12-24 1987-10-06 Trw Automotive Products, Inc. Gas generating material
US4806180A (en) * 1987-12-10 1989-02-21 Trw Vehicle Safety Systems Inc. Gas generating material

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2543971C2 (de) * 1975-10-02 1986-05-22 Dynamit Nobel Ag, 5210 Troisdorf Anzündsystem für hochtemperaturbeständige Treibmittel

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1168746A (en) * 1916-01-18 Du Pont Powder Co Composition for detonating explosive charges.
US1185830A (en) * 1913-06-30 1916-06-06 Du Pont Powder Co Detonator.
US1254147A (en) * 1913-04-17 1918-01-22 Ver Koln Rottweiler Pulverfabriken Initial igniter.
US1930765A (en) * 1931-01-03 1933-10-17 Meissner Josef Cartridge with primary and secondary charges
US2360698A (en) * 1939-05-17 1944-10-17 Trojan Powder Co Detonator

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1168746A (en) * 1916-01-18 Du Pont Powder Co Composition for detonating explosive charges.
US1254147A (en) * 1913-04-17 1918-01-22 Ver Koln Rottweiler Pulverfabriken Initial igniter.
US1185830A (en) * 1913-06-30 1916-06-06 Du Pont Powder Co Detonator.
US1930765A (en) * 1931-01-03 1933-10-17 Meissner Josef Cartridge with primary and secondary charges
US2360698A (en) * 1939-05-17 1944-10-17 Trojan Powder Co Detonator

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3873579A (en) * 1969-08-20 1975-03-25 Us Navy Organic azides and method of preparation thereof
JPS49100209A (enrdf_load_stackoverflow) * 1973-02-02 1974-09-21
JPS5082212A (enrdf_load_stackoverflow) * 1973-11-29 1975-07-03
US4428292A (en) 1982-11-05 1984-01-31 Halliburton Company High temperature exploding bridge wire detonator and explosive composition
US4696231A (en) * 1986-02-25 1987-09-29 E. I. Du Pont De Nemours And Company Shock-resistant delay detonator
US4696705A (en) * 1986-12-24 1987-09-29 Trw Automotive Products, Inc. Gas generating material
US4698107A (en) * 1986-12-24 1987-10-06 Trw Automotive Products, Inc. Gas generating material
US4806180A (en) * 1987-12-10 1989-02-21 Trw Vehicle Safety Systems Inc. Gas generating material

Also Published As

Publication number Publication date
BE713570A (enrdf_load_stackoverflow) 1968-08-16
NL6805196A (enrdf_load_stackoverflow) 1968-10-14
CH491060A (de) 1970-05-31
IL29794A (en) 1972-05-30
DE1646336B2 (de) 1975-11-13
DE1646336A1 (de) 1971-07-08
FR1562370A (enrdf_load_stackoverflow) 1969-04-04
IL29794A0 (en) 1969-04-30
GB1189952A (en) 1970-04-29

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