US2257360A - Desensitized pentaerythritol tetranitrate explosive - Google Patents

Desensitized pentaerythritol tetranitrate explosive Download PDF

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US2257360A
US2257360A US317903A US31790340A US2257360A US 2257360 A US2257360 A US 2257360A US 317903 A US317903 A US 317903A US 31790340 A US31790340 A US 31790340A US 2257360 A US2257360 A US 2257360A
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pentaerythritol tetranitrate
explosive
mixture
desensitized
pentaerythritol
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US317903A
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Joseph A Wyler
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Trojan Powder Co
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Trojan Powder Co
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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
    • C06B25/32Compositions containing a nitrated organic compound the compound being nitrated pentaerythritol
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S149/00Explosive and thermic compositions or charges
    • Y10S149/11Particle size of a component

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  • This invention relates in general to explosive compositions and more particularly to desensitized pentaerythritol tetranitrate explosives.
  • pentaerythritol tetranitrate possesses the disadvantageous property of being unusually sensitive to friction and impact. It is also known, although not so commonly, that pentaerythritol tetr-anitrate is very sensitive to detonation even when wetted with an equal weight of water. These factors are the main reason why pentaerythritol tetranitrate has not found greater usefulness, although many of its other explosive properties are of a distinctly superior nature.
  • the present invention is concerned with the preparation of certain pentaerythritol tetranitrate explosive mixtures having low friction and impact sensitiveness and at the same time having excellent sensitivity toward detonation by means of the usual initiators used in the explosives industry.
  • Example 1 22 lbs. of Ca(N03)z-ell20 are placed in a steam jacketed graining kettle provided with a suitable stirrer, and heated to a temperature alcove 40 C. in order to produce a thin liquid. Then 78 lbs. of pentaerythritol tetranitrate (preferably previously heated to above 40 C.) are incorporated into this liquid by stirring the mixture at a temperature above the melting point of the hydrous calcium nitrate. After about fifteen minutes of this stirring the mixture is allowed to cool slowly, with further stirring, until .a granular or pul verulent mixture results. This mixture is then passed through an 18 mesh sieve to produce my preferred product.
  • pentaerythritol tetranitrate preferably previously heated to above 40 C.
  • Example 2 Ninety pounds of a mixture consisting of:
  • I may prepare mixtures of pentaerythritol tetranitrate with any of the hydrated calcium nitrates which melt below 100 C. Also, I may use mixtures of these calcium nitrates 'mixture as would be obtained if finely crystalline pentaerythritol tetranitrate and finely powdered nitrates are simply mixed below the melting point of the nitrates.
  • My compositions are characterized by the individual crystals or agglomerations of crystals of pentaerythritol tetranitrate being imbedded within the solidified nitrate and by the resulting mixture consisting of discrete particles which may be, spherical, granular or pulverulent. These mixtures are capable of being poured or pressed into molds or used in admixture with other materials commonly used in commercial explosives.
  • My pentaerythrltol tetranitrate compositions are useful directly as explosives, as for example, a mixture consisting of 78 parts (by weight) of pentaerythritol tetranitrate and 22 parts (by weight) of Ca(NOs) ll-I20 which'is essentially oxygen-balanced, has an unusually high brisance and is adapted for special uses where high shattering ability is required.
  • Compositions containing more of the nitrates than is required for an are not intended to limit me to the method given therein, for the preparation of my compositions.
  • oxygen balance (all C to form CO2, all Hz to form, H2O, the metals to form oxides and the nitrogen to be liberatedas N2) are particularly useful for admixture with oxygen-deficient explosives as nitrostarch, nitrocellulose, trinitrotoluene, dinitrotoluene, dipentaerythritol hexanitrate, tetryl, nitrated alkyl lactates, nitrated alkyl glycollates, etc., or mixtures of these with oxidizing agents as NH4NO3, NaNOa, and the like or with reducing agents as woodpulp, charcoal, ivory nuta parafin rOsin, mineral oils, vaseline, and the like; or with oxygen-deficient or combustiblematerials in general. h,
  • pentaerythritol tetranitrate in, abroad manner.
  • Persons familiar with the explosives art know that all commercial pentaerythi itol tetranitrate contains some dipentaerythritol hexanitrate (often as much as l0-l2%) and, at times, other impurities absorbed from the mother liquor obtained in the pentaerythritol crystallization. Consequently, the term. pentaerythritol tetranitrate is used not only to mean pure pentaerythritol tetranitrate, but also the impure product normally obtained by the various commercial processes.
  • I wish to emphasize that the examples given above are merely illustrative of my invention and I may, for instance, melt the hydrated-nitratemixtures, stir, add the pentaerythritol tetranitrate, stir, then allow the molten mixture to flow in the form of a thin stream, and then be subjected to a jet ofair under high pressure so as to form small globules which upon falling through the cool air, solidify and form spheres; or I may use any suitable process which produces the product of characteristics described above. I, therefore, do not, limit myself in any way except as indicated in the following claims.
  • An. explosive comprising pentaerythritol tetranitrate and a hydrated calcium nitrate of melting point greater than 35 C. and less than.
  • said pentaerythritol tetranitrate being substantially embedded within the hydrated nitrates and the mixture being composed of discrete particles.
  • An explosive comprising pentaerythritol tetranitrate and Ca(NO3) -4H2O, said pentaerythritol tetranitrate being substantially embedded within the hydrated nitrate and the mixture being composed of discrete particles.
  • a composition of matter comprising pentaerythritol tetranitrate and Ca(NOa)2-4H2O' in the proportions, by weight, of approximately '78 parts of pentaerythritol tetranitrate to 22 parts of Ca(NOa)z-4H2O, said composition being made up of solid, discrete particles in which the pentaerythritol tetranitrate is substantially embedded within the Ca(N0a)2-4H2O.
  • An explosive comprising crystalline pentaerythritol tetranitrate, hydrated calcium nitrate of melting point between 35 C. and 100 (3., and an oxygen-deficient explosive; said pentaerythritol tetranitrate being substantially embedded within the hydrated calcium nitrate and this resulting mixture of pentaerythritol tetranitrate and hydrated calcium nitrate being composed of discrete particles; and said oxygen-deficient explosive being intimately mixed with the pentaerythritol tetranitrate-calcium nitrate mixture.
  • An explosive comprising crystalline pentaerythritol tetranitrate, hydrated calcium nitrate of melting point between 35 C. and 100 (3., and nitrostarch; said pentaerythritol tetranitrate being substantially embedded within the hydrated calcium nitrate and this resulting mixture 7 of pentaerythritol tetranitrate and hydrated calcium nitrate being composed of discrete particles; and said nitrostarch being intimately mixed with the pentaerythritol tetranitrate calcium nitrate mixture.

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

Description

atenied Sept: 9 3943 "rr er DESENSITIZED PENTAERYTHTOL TETRA- I NE'ERATE EHLOSIVE .loseph A. Wyler, Allentown, Pa; assignor to Trojan Eowder Company, Allento, lPa.
No Drawing. Application February a, 1940, Serial No. 317,903
@laims.
This invention relates in general to explosive compositions and more particularly to desensitized pentaerythritol tetranitrate explosives.
It is well known that pentaerythritol tetranitrate possesses the disadvantageous property of being unusually sensitive to friction and impact. It is also known, although not so commonly, that pentaerythritol tetr-anitrate is very sensitive to detonation even when wetted with an equal weight of water. These factors are the main reason why pentaerythritol tetranitrate has not found greater usefulness, although many of its other explosive properties are of a distinctly superior nature.
The present invention is concerned with the preparation of certain pentaerythritol tetranitrate explosive mixtures having low friction and impact sensitiveness and at the same time having excellent sensitivity toward detonation by means of the usual initiators used in the explosives industry.
l have discovered that the hydrated calcium nitrates as Ca(l\TOa)2-3H2O, Ca(NO3)2'4-H2O and Ca (N03) z-XHzO, which melt at temperatures less than 100 C. can be used in combination with pentaerythritol tetranitrate to produce granular or pulverulent mixtures of excellent explosive properties.
in order to more clearly point out my. invention, the following examples are given by way of illustration:
Example 1 22 lbs. of Ca(N03)z-ell20 are placed in a steam jacketed graining kettle provided with a suitable stirrer, and heated to a temperature alcove 40 C. in order to produce a thin liquid. Then 78 lbs. of pentaerythritol tetranitrate (preferably previously heated to above 40 C.) are incorporated into this liquid by stirring the mixture at a temperature above the melting point of the hydrous calcium nitrate. After about fifteen minutes of this stirring the mixture is allowed to cool slowly, with further stirring, until .a granular or pul verulent mixture results. This mixture is then passed through an 18 mesh sieve to produce my preferred product.
In a similar manner I have prepared mixtures kettle provided with a stirrer.
oi C3.(NO3) 2-4n2o and pentaerythritol tetranitrate of following compositions and properties:
Grams fulminate of mgnury regtandard drop quire 0 cause ammer sensi- PETN CMNOQMHZO detonation of tiveness (10 kg.
(1" x 4" carweight) tridges) Percent Percent Centimelers 100 0 Less than .26 gms 5-10 95 5 Less than .26 gms.. 15 90 10 Less than .26 gms 40 80 20 Less than .26 gms 7O 30 Less than .26 gms 95-100 60 40 Less than .26 gins. 100+ 50 50 Less than .26 gms 100+ 30 .4 gm 100+ 20 (Partial detonation .65 gm. Detonates with .8 gm. 0 100 Non-explosive These results show that the addition of Ca (N03) 41-120 applied in the manner described above has a pronouncecl. effect upon the impact sensitiveness of pentaerythritol tetranitrate without causing a deleterious drop in the detonative sensitiveness toward the proper initiating agents.
Example 2 Ninety pounds of a mixture consisting of:
Percent CMNOs) 36.8 NI-lrNOa Q1 H20 19.1
are heated to above the melting point (below 100 C.) in a suitable steam jacketed we lhen 10 pounds of. pentaerythritol tetranitrate are added and the mixture stirred with cooling, until a granular or pulverulent product results. This product was detonatable by means of about .33 gm. of mercury fulminate and was insensitive toward impact (a 10 kg. weight did not cause a detonation when dropped from a height of 100 cm.)
Similarly, I may prepare mixtures of pentaerythritol tetranitrate with any of the hydrated calcium nitrates which melt below 100 C. Also, I may use mixtures of these calcium nitrates 'mixture as would be obtained if finely crystalline pentaerythritol tetranitrate and finely powdered nitrates are simply mixed below the melting point of the nitrates. My compositions are characterized by the individual crystals or agglomerations of crystals of pentaerythritol tetranitrate being imbedded within the solidified nitrate and by the resulting mixture consisting of discrete particles which may be, spherical, granular or pulverulent. These mixtures are capable of being poured or pressed into molds or used in admixture with other materials commonly used in commercial explosives.
My pentaerythrltol tetranitrate compositions are useful directly as explosives, as for example, a mixture consisting of 78 parts (by weight) of pentaerythritol tetranitrate and 22 parts (by weight) of Ca(NOs) ll-I20 which'is essentially oxygen-balanced, has an unusually high brisance and is adapted for special uses where high shattering ability is required. Compositions containing more of the nitrates than is required for an are not intended to limit me to the method given therein, for the preparation of my compositions.
oxygen balance (all C to form CO2, all Hz to form, H2O, the metals to form oxides and the nitrogen to be liberatedas N2) are particularly useful for admixture with oxygen-deficient explosives as nitrostarch, nitrocellulose, trinitrotoluene, dinitrotoluene, dipentaerythritol hexanitrate, tetryl, nitrated alkyl lactates, nitrated alkyl glycollates, etc., or mixtures of these with oxidizing agents as NH4NO3, NaNOa, and the like or with reducing agents as woodpulp, charcoal, ivory nuta parafin rOsin, mineral oils, vaseline, and the like; or with oxygen-deficient or combustiblematerials in general. h,
It is important to note that I am using the term, pentaerythritol tetranitrate in, abroad manner. Persons familiar with the explosives art know that all commercial pentaerythi itol tetranitrate contains some dipentaerythritol hexanitrate (often as much as l0-l2%) and, at times, other impurities absorbed from the mother liquor obtained in the pentaerythritol crystallization. Consequently, the term. pentaerythritol tetranitrate is used not only to mean pure pentaerythritol tetranitrate, but also the impure product normally obtained by the various commercial processes.
I wish to emphasize that the examples given above are merely illustrative of my invention and I may, for instance, melt the hydrated-nitratemixtures, stir, add the pentaerythritol tetranitrate, stir, then allow the molten mixture to flow in the form of a thin stream, and then be subjected to a jet ofair under high pressure so as to form small globules which upon falling through the cool air, solidify and form spheres; or I may use any suitable process which produces the product of characteristics described above. I, therefore, do not, limit myself in any way except as indicated in the following claims.
I claim:
- 1. An. explosive comprising pentaerythritol tetranitrate and a hydrated calcium nitrate of melting point greater than 35 C. and less than.
0., said pentaerythritol tetranitrate being substantially embedded within the hydrated nitrates and the mixture being composed of discrete particles.
2. An explosive comprising pentaerythritol tetranitrate and Ca(NO3) -4H2O, said pentaerythritol tetranitrate being substantially embedded within the hydrated nitrate and the mixture being composed of discrete particles.
3. A composition of matter comprising pentaerythritol tetranitrate and Ca(NOa)2-4H2O' in the proportions, by weight, of approximately '78 parts of pentaerythritol tetranitrate to 22 parts of Ca(NOa)z-4H2O, said composition being made up of solid, discrete particles in which the pentaerythritol tetranitrate is substantially embedded within the Ca(N0a)2-4H2O.
4. An explosive comprising crystalline pentaerythritol tetranitrate, hydrated calcium nitrate of melting point between 35 C. and 100 (3., and an oxygen-deficient explosive; said pentaerythritol tetranitrate being substantially embedded within the hydrated calcium nitrate and this resulting mixture of pentaerythritol tetranitrate and hydrated calcium nitrate being composed of discrete particles; and said oxygen-deficient explosive being intimately mixed with the pentaerythritol tetranitrate-calcium nitrate mixture.
5. An explosive comprising crystalline pentaerythritol tetranitrate, hydrated calcium nitrate of melting point between 35 C. and 100 (3., and nitrostarch; said pentaerythritol tetranitrate being substantially embedded within the hydrated calcium nitrate and this resulting mixture 7 of pentaerythritol tetranitrate and hydrated calcium nitrate being composed of discrete particles; and said nitrostarch being intimately mixed with the pentaerythritol tetranitrate calcium nitrate mixture.
JOSEPH A. WYLER.
US317903A 1940-02-08 1940-02-08 Desensitized pentaerythritol tetranitrate explosive Expired - Lifetime US2257360A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2548693A (en) * 1945-08-24 1951-04-10 Ici Ltd Process of producing explosives containing ammonium nitrate
US3127107A (en) * 1964-03-31 Generation of ice-nucleating crystal

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3127107A (en) * 1964-03-31 Generation of ice-nucleating crystal
US2548693A (en) * 1945-08-24 1951-04-10 Ici Ltd Process of producing explosives containing ammonium nitrate

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