US1404687A - Primary detonating composition - Google Patents

Primary detonating composition Download PDF

Info

Publication number
US1404687A
US1404687A US384734A US38473420A US1404687A US 1404687 A US1404687 A US 1404687A US 384734 A US384734 A US 384734A US 38473420 A US38473420 A US 38473420A US 1404687 A US1404687 A US 1404687A
Authority
US
United States
Prior art keywords
diazodinitrophenol
detonating
primary
composition
primary detonating
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
Application number
US384734A
Inventor
William M Dehn
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.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US384734A priority Critical patent/US1404687A/en
Application granted granted Critical
Publication of US1404687A publication Critical patent/US1404687A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/04Compositions containing a nitrated organic compound the nitrated compound being an aromatic

Definitions

  • This invention refers to the use of di- 10 azodinitrophenol (4.6-dinitro-2-diazophenol) as a substitute capable of replacing the fulminates, the azides, or other detonatmg compounds hitherto used in primary detonating charges.
  • diazodinitrophenol possesses a number of properties that characterize it as an excellent detonating explosive.
  • compounded of diazodinitrophenol and oxidiz'lng salts may be varied widely according to requirements.
  • diazodinitroplrenol Another great advantage of diazodinitroplrenol is its indifference toward water, as is evidenced by its non-hygroscopic nature and by itsv chemical stability when stored in water. This property permits of long stor age of its compositions, without loss of power, a contra-distinction to mercury fulminate which is especially subject to deterioration in moist air. Furthermore its non-hygroscopic nature requires no protecting admixed or superimposed materials and no special precautions for stora e.
  • Diazodinitrophenol is stable 1n the presence of acids, hence nitric acid and its'decomposition products, which may be evolved spontaneously from explosive compositions during storage, have little or no hazardous effects upon it.
  • I Diazodinitrophenol can be safely and powerfully compressed without loss of sensitiveness to explode, hence it and its explosive mixtures can be concentrated to favorable densities in detonating containers.
  • diazodinitrophenol The temperatures of meltingand ignition of diazodinitrophenol are above 150 degrees, hence diazodinitrophenol is favorably sensitive to combustion and to percussion.
  • Diazodinitrophenol can be manufactured cheaply from materials always easily avail- --able.
  • diazodinitrophenol yields detonating compositions more powerful than the usual detonating compositions of mercury fulminate.
  • the granulated or powdered mixtures of diazodinitrophenol and potassium chlorate can be made desirably fine grained and free running and can be loaded readily into detonating shells or other containers.
  • compositions are formed whose detonating strengths are substantially similar to the above described mixtures of diazodinitrophenol and potassium chlorate.
  • YVhereas my invention is capable of being carried out in many different ways, it is herein observed that it does not relate to secondary detonating, or booster charges, to be exploded by adjacent or superimposed primary detonatlng charges composed in accordance with my invention; nor does it relateto charges of mercury fulminate. used. as an intermediate to this booster and this adjacent or superimposed primary detonating charge composed in accordance with my inventlon.
  • tro phenol and potassium chlorate are intimately" intermixed and then themixture is run into detonating tubes,.casings or caps and'com'pressed to the required density.
  • composition varying within the above described limits may be compressed into tubes, casings or caps previously partly l.
  • a primary detonating composition comprising diazodinitrophenol and a chlorinecontaining oxidizing salt of a fixed alkali.
  • a primary detonating composition comprising diazodinitrophenol and a chlorinecontaining oxidizing salt of potassium.
  • a primary detonating composition comprising diazodinitrophenol and a chlorate of a fixed alkali.
  • a primary detonating composition comprising diazodinitrophenol and the chlorate of potassium mixed therewith, the detonating charge being highly compressed.
  • a detonator for explosive material comprising diazodinitrophenol.

Description

65 from mercury, lead and other UNITED STATES 325.5 litttKtNUx;
PATENT oFFicE.
WILLIAM H. DEBIT, OF SEATTLE, WASHINGTON.
PRIMARY DETONATING COMPOSITION.
1T0 Drawing.
T 0 all whom it may concern Be it known that I, WILLIAM M. DEHN, a citizen of the United States, residing at Seattle, in the county of King and State of Washington, have invented certain new and. useful Improvements in Primary Detonating Compositions, of which the followingis a specification.
This invention refers to the use of di- 10 azodinitrophenol (4.6-dinitro-2-diazophenol) as a substitute capable of replacing the fulminates, the azides, or other detonatmg compounds hitherto used in primary detonating charges.
I have found that diazodinitrophenol possesses a number of properties that characterize it as an excellent detonating explosive.
It contains no metals. Metallic compounds of hydrazoic'and fulminic acids have been used almost universally as the.explosive of the first class? in primer charges; that is to say, as the compound which is capable of causing the detonation of other explosives in contact therewith when it itself is However, when exploded in the presenceof ammonium nitrate it gives smokeless combustion products, substantially in accordance with the equation:
When exploded in the presence of the chlorates or the perchlorates of the alkali metals, it gives smoke composed of alkali chlorides which have little or no corrosive effects on metals of ordnance. Therefore, oxidizing accelerators may be used with diazodinitrophenol to form detonating compositions free eavy metals. The high capacity of diazodinitrophenol Specification of Letters Patent. Patented J an, 24,' 1922, Application filed May 27, 1920. Serial No. 384,734.
compounded of diazodinitrophenol and oxidiz'lng salts may be varied widely according to requirements.
Another great advantage of diazodinitroplrenol is its indifference toward water, as is evidenced by its non-hygroscopic nature and by itsv chemical stability when stored in water. This property permits of long stor age of its compositions, without loss of power, a contra-distinction to mercury fulminate which is especially subject to deterioration in moist air. Furthermore its non-hygroscopic nature requires no protecting admixed or superimposed materials and no special precautions for stora e.
Diazodinitrophenol is stable 1n the presence of acids, hence nitric acid and its'decomposition products, which may be evolved spontaneously from explosive compositions during storage, have little or no hazardous effects upon it. I Diazodinitrophenol can be safely and powerfully compressed without loss of sensitiveness to explode, hence it and its explosive mixtures can be concentrated to favorable densities in detonating containers.
The temperatures of meltingand ignition of diazodinitrophenol are above 150 degrees, hence diazodinitrophenol is favorably sensitive to combustion and to percussion.
Diazodinitrophenol can be manufactured cheaply from materials always easily avail- --able.
When measured by the sand test, diazodinitrophenol reveals eat power of demolition. Small quantities of it superimposed on ordinary explosive compositions cause complete explosions of the same. Its sensitiveness and brisance, therefore, admit of it being used as a substitute for the fulminates, the azides, and the other detonating explosives.
Under varied conditions of granulation, compression, and confinement, I have found that the strength of pure disazodinitrophenol is invariably greater than that of mixtures of potassium chlorate and mercury fulminate. When mixed with potassium chlorate in advantageous percentages it reveals substantially per cent greater powerthan the most efficient mixtures of %otassium chlorate and mercury fulminate.
ven with equal weight of potassium ch10:
rate, diazodinitrophenol yields detonating compositions more powerful than the usual detonating compositions of mercury fulminate. The granulated or powdered mixtures of diazodinitrophenol and potassium chlorate can be made desirably fine grained and free running and can be loaded readily into detonating shells or other containers.
\Vith the most effective masses of other oxidants, such as the nitrates, the perchlorates and the peroxides, compositions are formed whose detonating strengths are substantially similar to the above described mixtures of diazodinitrophenol and potassium chlorate.
YVhereas my invention is capable of being carried out in many different ways, it is herein observed that it does not relate to secondary detonating, or booster charges, to be exploded by adjacent or superimposed primary detonatlng charges composed in accordance with my invention; nor does it relateto charges of mercury fulminate. used. as an intermediate to this booster and this adjacent or superimposed primary detonating charge composed in accordance with my inventlon.
Whereas my invention is capable of embodiment in many different forms, for the tro phenol and potassium chlorate are intimately" intermixed and then themixture is run into detonating tubes,.casings or caps and'com'pressed to the required density.
C.A mixture of 70 parts of diazodinitrophenol and30 parts of potassium chlorate is first prepared and then iscompressed to the required density in detonating tubes, casings-or caps. x
D. The composition varying within the above described limits may be compressed into tubes, casings or caps previously partly l. A primary detonating composition comprising diazodinitrophenol and a chlorinecontaining oxidizing salt of a fixed alkali.
5. A primary detonating composition comprising diazodinitrophenol and a chlorinecontaining oxidizing salt of potassium.
6. A primary detonating composition comprising diazodinitrophenol and a chlorate of a fixed alkali.
7 primary detonating composition com prising diazodinitrophenol and the chlorate of potassium. I
8. A primary detonating composition comprising diazodinitrophenol and the chlorate of potassium mixed therewith, the detonating charge being highly compressed.
9. A detonator for explosive material comprising diazodinitrophenol.
In witness whereof, I have signed my name hereto.
WILLIAM DEHN.
US384734A 1920-05-27 1920-05-27 Primary detonating composition Expired - Lifetime US1404687A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US384734A US1404687A (en) 1920-05-27 1920-05-27 Primary detonating composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US384734A US1404687A (en) 1920-05-27 1920-05-27 Primary detonating composition

Publications (1)

Publication Number Publication Date
US1404687A true US1404687A (en) 1922-01-24

Family

ID=23518532

Family Applications (1)

Application Number Title Priority Date Filing Date
US384734A Expired - Lifetime US1404687A (en) 1920-05-27 1920-05-27 Primary detonating composition

Country Status (1)

Country Link
US (1) US1404687A (en)

Similar Documents

Publication Publication Date Title
US2929699A (en) Explosive
US1890112A (en) Igniter charge for blasting caps
US2011578A (en) Explosive
US2970900A (en) Priming composition
US1404687A (en) Primary detonating composition
US2154416A (en) Nondetonating blasting explosive
US2708623A (en) Explosive compound, process of making same and a composition thereof
US1797509A (en) Electric blasting cap and ignition material for the same
US2829036A (en) Fire damp proof explosive compositions
US2422043A (en) Compound detonator
US1984846A (en) Ignition composition
US953798A (en) Safety-powder for blasting.
US3357873A (en) Explosive composition comprising a nitric acid ester of a polyvalent alcohol and theternary salt mixture of ammonium chloride, an alkali nitrate, and an alkaline earth carbonate
US3310569A (en) Crystalline double salt of lead nitroaminotetrazole and lead styphnate
US1048207A (en) Priming mixture.
US1495350A (en) Priming composition
US1878652A (en) Process of initial detonating explosive matter and for the manufacture of detonating caps in accordance therewith
US1393984A (en) Explosive and process for manufacturing it
US3053710A (en) Magnesium hydride explosive compositions
US97566A (en) Improved explosive compound for use in fire-arms, blasting
US2425310A (en) Explosive
US2060522A (en) Nitrosoguanidine as a priming ingredient
US1533798A (en) Secondary charge for compound detonators
US3356546A (en) Safety blasting composition with a metal formate as a fuel
US768512A (en) Explosive compound.