US3466205A - Explosive containing hexogene or octogene and a nitrated n-methylaniline - Google Patents

Explosive containing hexogene or octogene and a nitrated n-methylaniline Download PDF

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Publication number
US3466205A
US3466205A US532528A US3466205DA US3466205A US 3466205 A US3466205 A US 3466205A US 532528 A US532528 A US 532528A US 3466205D A US3466205D A US 3466205DA US 3466205 A US3466205 A US 3466205A
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US
United States
Prior art keywords
hexogene
octogene
methylaniline
nitrated
mixture
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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US532528A
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English (en)
Inventor
Jacques Boileau
Gerard Desseigne
Jean Paul Konrat
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ARMEES FRANCE
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ARMEES FRANCE
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Publication of US3466205A publication Critical patent/US3466205A/en
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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
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0033Shaping the mixture
    • C06B21/005By a process involving melting at least part of the ingredients
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/34Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine

Definitions

  • An explosive composition which does not exude at temperatures below 100 C. comprises at least one of hexogene (cyclotrimethylenetrinitramine) or octogene (eyclotetramethylenetetranitramine) in intimate mixture with at least one of 2,4,6-trinitro-N-methylaniline or 2,4,6-trinitro-N,N'-dimethylaniline.
  • the composition may also contain at least one additive of the group consisting of waxes, graphite and metallic powders.
  • one method of filling munitions comprises pouring a fluid explosive mixture, which then solidifies and hardens.
  • explosive mixtures include on the one hand tolite (trinitrotoluene, TNT) and on the other hand nitramines such as hexogene (cyclotrimethylenetrinitramine) or octogene (cyclotetramethylenetetranitramine) and also, as required, one or more other materials such as wax, graphite and, metallic powders.
  • the present invention thus relates to explosive compositions containing:
  • compositions can also contain other additives, such as waxes, graphite and metallic powders.
  • present invention also relates to the means for obtaining these compositions. Having regard to the high melting points of the nitrated derivatives, hot water coating at ordinary pressure cannot be used.
  • METHOD 1 The direct introduction of dry hexogene or octogene into the trinitromethylaniline or trinitrodimethylaniline is the most simple method for making the mixture, but it has the disadvantage of requiring the drying of pure hexogene or octogene, which are explosives offering considerable risks when handled whilst dry.
  • METHOD 2 It is of advantage therefore to prepare, for instance by one or other of methods 3 and 4, a composition containing, for example, 90 of hexogene or octogene covered with 10% of the nitrated aniline, in order to phlegmatise or otherwise protect the hexogene or octogene.
  • This dry granular composition is then introduced into a bath of the molten nitrated aniline, as is the current practice in the case of hexogene/tolite mixtures.
  • the third method mentioned consists in coating hexogene or octogene with the nitrated aniline in water under pressure, the temperature being sufliciently high for the nitrated aniline to be molten, the upper limit being given by the temperature of hydrolysis of hexogene (about C.) or of octogene (about C.).
  • the fourth method is utilisable with a solvent which is immiscible or slightly miscible with water and involves dissolving the trinitromethylaniline or trinitrodimethylaniline.
  • This solvent will be subsequently entrained with steam and it will remain in suspension in the water from the composition desired.
  • Solvents which can be used include, for instance, aromatic hydrocarbons, nitroparaffins, esters, ketones and other oxides.
  • Examples (1) g. of 2,4,6-trinitro-N-methylaniline were dissolved in a flask maintained at 120 C. by means of an oil bath. g. of hexogene recrystallised from cyclohexanone were added in stages with stirring. The mixture was then poured into a small flat dish. A yellow plate of the mixture desired was thus obtained. This pouring can also be made into a glass tube which has previously been evacuated. After cooling a cartridge is obtained having a speed of detonation (7750 m./s.) which is substantially the same as that of a cartridge of 60% hexogene, 40% tolite. The stability under vacuum at 130 C. of this mixture is better than that of a 60/40 hexogene/tolite mixture under the same conditions.
  • An explosive composition which does not exude below 100 C., which consists essentially of at least one substance selected from the group consisting of hexogene and octogene plus at least one substance selected from the group consisting of 2,4,6-trinitro-N-methylaniline and 2,4,6-trinitro-N,N-dimethylaniline in intimate mixture therewith.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
US532528A 1965-03-01 1966-02-28 Explosive containing hexogene or octogene and a nitrated n-methylaniline Expired - Lifetime US3466205A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7444A FR1535427A (fr) 1965-03-01 1965-03-01 Composition explosive

Publications (1)

Publication Number Publication Date
US3466205A true US3466205A (en) 1969-09-09

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ID=8572351

Family Applications (1)

Application Number Title Priority Date Filing Date
US532528A Expired - Lifetime US3466205A (en) 1965-03-01 1966-02-28 Explosive containing hexogene or octogene and a nitrated n-methylaniline

Country Status (6)

Country Link
US (1) US3466205A (ko)
DE (1) DE1301271B (ko)
FR (1) FR1535427A (ko)
GB (1) GB1134564A (ko)
LU (1) LU49966A1 (ko)
NL (1) NL6515939A (ko)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3994756A (en) * 1975-11-26 1976-11-30 The United States Of America As Represented By The Secretary Of The Army Castable composite explosive compositions containing a mixture of trinitrobenzene and trinitroxylene
US4747892A (en) * 1987-05-22 1988-05-31 The United States Of America As Represented By The Secretary Of The Air Force Melt-castable explosive composition

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2738562B1 (fr) * 1995-09-08 1997-10-03 Poudres & Explosifs Ste Nale Compositions explosives coulees-fondues
FR2750131B1 (fr) * 1996-06-19 1998-07-17 Giat Ind Sa Composition explosive fusionnable/coulable et a vulnerabilite reduite
RU2443665C1 (ru) * 2010-07-12 2012-02-27 Федеральное государственное унитарное предприятие "Научно-исследовательский институт полимерных материалов" Способ модификации октогена

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000720A (en) * 1959-04-09 1961-09-19 Baer Maurice Desensitization of cyclotrimethylenetrinitramine with dinitroethylbenzene
US3138496A (en) * 1961-06-13 1964-06-23 Commercial Solvents Corp Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax
US3297503A (en) * 1965-09-21 1967-01-10 Paul O Hoffmann Cyclotol and thermite explosive composition

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE166804C (ko) *
US1045012A (en) * 1911-02-04 1912-11-19 Bernhard Jacques Fluerscheim Explosive.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000720A (en) * 1959-04-09 1961-09-19 Baer Maurice Desensitization of cyclotrimethylenetrinitramine with dinitroethylbenzene
US3138496A (en) * 1961-06-13 1964-06-23 Commercial Solvents Corp Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax
US3297503A (en) * 1965-09-21 1967-01-10 Paul O Hoffmann Cyclotol and thermite explosive composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3994756A (en) * 1975-11-26 1976-11-30 The United States Of America As Represented By The Secretary Of The Army Castable composite explosive compositions containing a mixture of trinitrobenzene and trinitroxylene
US4747892A (en) * 1987-05-22 1988-05-31 The United States Of America As Represented By The Secretary Of The Air Force Melt-castable explosive composition

Also Published As

Publication number Publication date
LU49966A1 (ko) 1967-06-01
FR1535427A (fr) 1968-08-09
NL6515939A (ko) 1968-09-25
GB1134564A (en) 1968-11-27
DE1301271B (de) 1969-08-14

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