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US1962065A - Process for the manufacture of explosive materials - Google Patents

Process for the manufacture of explosive materials Download PDF

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Publication number
US1962065A
US1962065A US445526A US44552630A US1962065A US 1962065 A US1962065 A US 1962065A US 445526 A US445526 A US 445526A US 44552630 A US44552630 A US 44552630A US 1962065 A US1962065 A US 1962065A
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manufacture
explosive
nitrates
explosive materials
alcohols
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US445526A
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Friederich Walter
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound

Definitions

  • the pentaerythrite-tetranitrate also has been used in manufacturing smokeless gunpowders, as well as for numerous other purposes, as per example for charging of blasting caps, of detonating fuses and preparation of difierent explosive charges.
  • the ketone alcohols and the cyclic alcohols have been partly described in literature. They result from the condensation of cyclic ketones with formaldehyde in the presence of alkalies or alkaline earths and other alkaline reaction materials. The cyclic alcohols by means of reduction also arise from the respective ketone alcohols. They all may be produced synthetically.
  • the nitrates of these bodies are very invariable and durable. They withstand long storing at 50 C. without any symptoms of decomposition being noted. Naturally the nitrates of the pure cyclic alcohols have more energetic strength than the ketone alcohols. The melting points of the nitrates are thus that they may be used either separately or in combination with one another or with other explosive materials for the manufacture of cast explosive charges. The velocity of detonation of the nitrates is very high and surpasses sometimes 8000 111 per second. These explosives are less sensitive against mechanical stress than the pentaerthrite-tetranitrate. Up to date no explosive materials are known having a similar energetic force and which can be cast at a temperature under 100 C. These explosives thus mean an important progress in the art of making cast explosive charges the more because some of the initial materials are already commercial products and others may be produced by synthetical processes.
  • An explosive composition comprising tetramethylol-cyclopentanol-tetranitrate.
  • An explosive composition comprising tetramethylol-cyclopentanone-tetranitrate.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Patented June 5, 1934 UNITED STATES PATENT? FFICE PROCESS FOR THE MANUFACTURE OF EXPLOSIVE MATERIALS Walter Friederich, Troisdorf, Germany 3 Claims.
The nitrates of pentaerythrite and of anhydroenneaheptite have been proposed for the use for very difierent purposes, as per example for the manufacture of detonating caps, detonating fuses,
5 artillery explosive shells and explosive charges of any kind. The pentaerythrite-tetranitrate also has been used in manufacturing smokeless gunpowders, as well as for numerous other purposes, as per example for charging of blasting caps, of detonating fuses and preparation of difierent explosive charges.
I now have ascertained that the cyclic ketone alcohols, tetramethylolcyclopentanone, tetramethylolcyclohexanone, as well as their reduction products, the cyclic alcohols, tetramethylolcyclopentanol, tetramethylolcyclohexanol, are forming nitrates when nitrated with concentrated nitric acid or with mixed acid. These nitrates thus obtained are not known up to now. The ketone alcohols and the cyclic alcohols have been partly described in literature. They result from the condensation of cyclic ketones with formaldehyde in the presence of alkalies or alkaline earths and other alkaline reaction materials. The cyclic alcohols by means of reduction also arise from the respective ketone alcohols. They all may be produced synthetically.
The nitrates of these bodies are very invariable and durable. They withstand long storing at 50 C. without any symptoms of decomposition being noted. Naturally the nitrates of the pure cyclic alcohols have more energetic strength than the ketone alcohols. The melting points of the nitrates are thus that they may be used either separately or in combination with one another or with other explosive materials for the manufacture of cast explosive charges. The velocity of detonation of the nitrates is very high and surpasses sometimes 8000 111 per second. These explosives are less sensitive against mechanical stress than the pentaerthrite-tetranitrate. Up to date no explosive materials are known having a similar energetic force and which can be cast at a temperature under 100 C. These explosives thus mean an important progress in the art of making cast explosive charges the more because some of the initial materials are already commercial products and others may be produced by synthetical processes.
The structural formulae of the compounds mentioned are the following:
Tetramethylolcyclopentanone HzC-C=(CH2OH)2 H2 0=x Hz &=(CH2OH)3 where X=HOH or=O.
2. An explosive composition comprising tetramethylol-cyclopentanol-tetranitrate.
3. An explosive composition comprising tetramethylol-cyclopentanone-tetranitrate.
WALTER FRIEDERICH.
US445526A 1929-10-10 1930-04-18 Process for the manufacture of explosive materials Expired - Lifetime US1962065A (en)

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DE1962065X 1929-10-10

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US445526A Expired - Lifetime US1962065A (en) 1929-10-10 1930-04-18 Process for the manufacture of explosive materials

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2698228A (en) * 1944-12-30 1954-12-28 John F Kincaid Flashless propellant

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2698228A (en) * 1944-12-30 1954-12-28 John F Kincaid Flashless propellant

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