US1883045A - Explosive composition - Google Patents

Explosive composition Download PDF

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Publication number
US1883045A
US1883045A US576436A US57643631A US1883045A US 1883045 A US1883045 A US 1883045A US 576436 A US576436 A US 576436A US 57643631 A US57643631 A US 57643631A US 1883045 A US1883045 A US 1883045A
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United States
Prior art keywords
dinitrate
dimethyl methane
explosive composition
dimethylol dimethyl
compound
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Expired - Lifetime
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US576436A
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Charles P Spaeth
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EIDP Inc
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EI Du Pont de Nemours and Co
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Priority to US576436A priority Critical patent/US1883045A/en
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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 nitration of dimethylol dimethyl methane may be brought about by various methods of procedure. For example, I may add the compound to concentrated sulfuric acid until it is completely dissolved, and then add this solution to concentrated nitric acid. I prefer, however, to nitrate by direct addition of the compound to a mixed acid of the approximate composition, sulfuric acid, and 45% nitric acid. I find the nitration to take place satisfactorily if the initial temperature is 2530 C., the temperature of the mixture being raised to 40 C. after the addition has been completed. The resulting compound separates rapidly from the waste acids and may be washed and neutralized in the usual manner.
  • Dimethylol dimethyl methane dinitrate is a liquid, having a slightly yellow color and a viscosity lower than that of nitroglycerin.
  • the pure product has a nitrogen content of 14.43%.
  • dimethylol dimethyl methane dinitrate has valuable properties when incorporated in explosive compositions. It may, for example, be used in nitroglycerin explosives as a freezing point depressant for the nitroglycerin. As such it is an active explosive compound as well as a freezing point EXPLOSIVE COMPOSITION Application filed November 20, 1931. Serial No. 576,436.
  • a high explosive composition in which dimethylol dimethyl methane dinitrate is incorporated
  • the following example of a gelatin dynamite is given While the foregoing example is a specific embodiment for an explosive composition in which dimethyl o1 dimethyl methane dinitrate is used, it is to be understood that other embodiments exist and may be practiced Within the scope of my invention, and that many variations in the composition may be used.
  • ethylene glycol dinitrate, or other of the known substitutes for nitroglycerin may be used with this compound.
  • ammonium nitrate may be. used if desired as an additional oxidizing agent, and as a substitute for a portion of the nitric ester content.
  • propellent powder compositions containing dimethylol dimethyl methane dinitrate may be prepared, and in order to illustrate such compositions more fully, the following examples are given:
  • a dynamite composition comprising nitrocellulose, gelatinized With a liquid nitric ester, and containing dimethylol dimethyl methane dinitrate.
  • a dynamite composition comprising nitroglycerin, nitrocellulose, one or more oxidizing agents, a carbonaceous combustible ingredient, and dimethylol dimethyl methane dinitrate.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Patented Oct. 18, 1932 STATES lama CHARLES P. SPAETH, OF WOODIBUBY, NEW JERSEY, ASSIGNOR TO E. I. DU PONT DE NEMOURS & COMPANY, OF WILMINGTON, DELAWARE, A CORPORATION OF DELA- WARE No Drawing.
'compound contains two methylol groups available for nitration.
I have found that, when the foregoing compound is treated with nitric acid under the proper conditions, dimethylol dimethyl methane dinitrate is formed according to the following reaction:
omon 0H=Noe +2HNOI= (Uriah-C +2H10 CHzOH CHzNO:
The nitration of dimethylol dimethyl methane may be brought about by various methods of procedure. For example, I may add the compound to concentrated sulfuric acid until it is completely dissolved, and then add this solution to concentrated nitric acid. I prefer, however, to nitrate by direct addition of the compound to a mixed acid of the approximate composition, sulfuric acid, and 45% nitric acid. I find the nitration to take place satisfactorily if the initial temperature is 2530 C., the temperature of the mixture being raised to 40 C. after the addition has been completed. The resulting compound separates rapidly from the waste acids and may be washed and neutralized in the usual manner.
Dimethylol dimethyl methane dinitrate, as prepared, is a liquid, having a slightly yellow color and a viscosity lower than that of nitroglycerin. The pure product has a nitrogen content of 14.43%.
I have found also that dimethylol dimethyl methane dinitrate has valuable properties when incorporated in explosive compositions. It may, for example, be used in nitroglycerin explosives as a freezing point depressant for the nitroglycerin. As such it is an active explosive compound as well as a freezing point EXPLOSIVE COMPOSITION Application filed November 20, 1931. Serial No. 576,436.
depressant. It has the advantage over n1- trated polymerized glycerin in such use that it does not unduly retard the gelatinization of the nitroglycerin by the nitrocotton.
As illustrative of a high explosive composition in ,which dimethylol dimethyl methane dinitrate is incorporated, the following example of a gelatin dynamite is given While the foregoing example is a specific embodiment for an explosive composition in which dimethyl o1 dimethyl methane dinitrate is used, it is to be understood that other embodiments exist and may be practiced Within the scope of my invention, and that many variations in the composition may be used. For example, ethylene glycol dinitrate, or other of the known substitutes for nitroglycerin may be used with this compound. Also ammonium nitrate may be. used if desired as an additional oxidizing agent, and as a substitute for a portion of the nitric ester content.
I have also found that propellent powder compositions containing dimethylol dimethyl methane dinitrate may be prepared, and in order to illustrate such compositions more fully, the following examples are given:
Emample I I P rt Nitrocellulose (12.85 to 13.35%N.) f Dimethylol dimethyl methane 30 Petroleum jelly 5 Ewample I] I P. rt Nitrocellulose (12.85 to 13.35% N.) 65 to 9d Di methylol dimethyl methane 35 to 10 Diphenylamine or other stabilizer Nitrocellulose (12.85 to 13.35% N.) 65 Nitroglycerin 5 to 25 Dimethylol dimethyl methane 25 to 5 Petroleum j e1ly 5 It Will therefore be understood that I am not to be limited in the scope of my invention except as indicated in the following patent claims.
I claim:
1. As a new compound dimethylol dimethyl methane dinitrate.
2. An explosive composition containing as an ingredient dimethylol dimethyl methane dinitrate. v 3. A propellent explosive Containing as an ingredient dimethylol dimethyl methane dinitrate.
4L. A dynamite composition containing dimethylol dimethyl methane dinitrate as an ingredient.
5. A dynamite composition comprising nitrocellulose, gelatinized With a liquid nitric ester, and containing dimethylol dimethyl methane dinitrate.
6. A dynamite composition comprising nitroglycerin, nitrocellulose, one or more oxidizing agents, a carbonaceous combustible ingredient, and dimethylol dimethyl methane dinitrate.
In testimony whereof I aifix my signature.
CHARLES P. SPAETH.
US576436A 1931-11-20 1931-11-20 Explosive composition Expired - Lifetime US1883045A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998015521A1 (en) * 1996-10-10 1998-04-16 Isis Pharma Gmbh New pentaerythritol derivatives, their production and use and intermediates for their synthesis
US7152509B2 (en) 2005-02-25 2006-12-26 Irwin Industrial Tool Company Fastener extractor

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998015521A1 (en) * 1996-10-10 1998-04-16 Isis Pharma Gmbh New pentaerythritol derivatives, their production and use and intermediates for their synthesis
US6180664B1 (en) 1996-10-10 2001-01-30 Isis Pharma Gmbh Pentaerythritol derivatives, their production and use and intermediates for their synthesis
US7152509B2 (en) 2005-02-25 2006-12-26 Irwin Industrial Tool Company Fastener extractor

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