US2011578A - Explosive - Google Patents
Explosive Download PDFInfo
- Publication number
- US2011578A US2011578A US2011578DA US2011578A US 2011578 A US2011578 A US 2011578A US 2011578D A US2011578D A US 2011578DA US 2011578 A US2011578 A US 2011578A
- Authority
- US
- United States
- Prior art keywords
- explosive
- ethylenedinitramine
- explosives
- shock
- brisance
- 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
Links
- 239000002360 explosive Substances 0.000 title description 62
- QCOXCILKVHKOGO-UHFFFAOYSA-N N-(2-nitramidoethyl)nitramide Chemical compound [O-][N+](=O)NCCN[N+]([O-])=O QCOXCILKVHKOGO-UHFFFAOYSA-N 0.000 description 28
- 230000035939 shock Effects 0.000 description 18
- 239000000203 mixture Substances 0.000 description 14
- OXNIZHLAWKMVMX-UHFFFAOYSA-N Picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 description 10
- 238000005474 detonation Methods 0.000 description 10
- 229940114148 picric acid Drugs 0.000 description 10
- 229950002929 trinitrophenol Drugs 0.000 description 10
- OFDYMSKSGFSLLM-UHFFFAOYSA-N Dinitramine Chemical compound CCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C(N)=C1[N+]([O-])=O OFDYMSKSGFSLLM-UHFFFAOYSA-N 0.000 description 8
- SNIOPGDIGTZGOP-UHFFFAOYSA-N 1,2,3-propanetrioltrinitrate Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 6
- AGUIVNYEYSCPNI-UHFFFAOYSA-N Tetryl Chemical group [O-][N+](=O)N(C)C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O AGUIVNYEYSCPNI-UHFFFAOYSA-N 0.000 description 6
- 229960003711 glyceryl trinitrate Drugs 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- HHEFNVCDPLQQTP-UHFFFAOYSA-N Ammonium perchlorate Chemical compound [NH4+].[O-]Cl(=O)(=O)=O HHEFNVCDPLQQTP-UHFFFAOYSA-N 0.000 description 4
- VKJKEPKFPUWCAS-UHFFFAOYSA-M Potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 230000002349 favourable Effects 0.000 description 4
- 239000003999 initiator Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 description 2
- NXEMFHROMKRKEG-UHFFFAOYSA-N 2,3,5,6-tetranitroaniline Chemical compound NC1=C([N+]([O-])=O)C([N+]([O-])=O)=CC([N+]([O-])=O)=C1[N+]([O-])=O NXEMFHROMKRKEG-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- -1 compound ethylenediaminedinitrate Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000000977 initiatory Effects 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000004642 transportation engineering Methods 0.000 description 2
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B29/00—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate
- C06B29/22—Compositions containing an inorganic oxygen-halogen salt, e.g. chlorate, perchlorate the salt being ammonium perchlorate
Definitions
- the subject of this invention is an explosive.
- This invention relates to an explosive -compo sition in which ethylenedinitramine is an essential constituent.
- ethylenedinitramine is an explosive and that it possesses some unusual properties which render it of special interest for various purposes. Outstanding among these properties is its high degree of resistance to detonation by impact or shock as compared to other explosives having equivalent brisance or explosive strength. It is generally recognized that high explosives which have an especially high degree of brisance or shattering effect are commonly more susceptible to detonation by impact or shock than other high explosives having appreciably lower brisance.
- nitroglycerine, pentaerythritetranitrate, trimethylenetrinitramine, tetranitroaniline and tetryl which are, among the most brisant high explosives which have found military or commercial use are all fairly sensitive to impact or shock. In fact they are so sensitive in this respect that they have not been used as bursting charges for shell or bombs but only considered for use in the form of small charges as boosters or initiators for the main bomb or shell charges. In the form of these small charges they are-not subjected to as rough usage as are the explosives which are handled in large quantity and used as-shell or bomb fillers.
- ethylenedinitramine has brisance or strength comparable to the explosives above mentioned but possesses greater resistance to detonation by shock than any of the explosives mentioned. Actually it corresponds in resistance to shock more nearly to the class of relative insensitive explosives such as picric acid, TNT, etc., which have been used as bursting charges. In the standard droptestit required a 10 inch height of fall of-a 2 kg. weight to cause detonation, this being exactly the same height of fall as was required for picric acid, but the dinitramine showed under test appreciably higher brisance or strength than either picric acid or TNT.
- ethylenedinitramine Another important characteristic of ethylenedinitramine is its relatively low ignition temperature. It explodes spontaneously when heated to a temperature of 180 closely to mercury fulmate and nitroglycerine in the ease with which it is detonated by heat. No
- Ethylenedinitramine has been found to be substantially insoluble in water only 0.5 gram dissolving in grams of water at 25 C. It has a high degree of stability, withstanding the standard C. Vacuum Stability Test as well as tetryl which has sufiicient stability that it has been widely used in both military and commercial detonators. I have found also that ethylenedinitramine is highly resistant to absorption of moisture from the air as indicated by the fact that when exposed to an atmosphere of 90% relative humidity at a temperature of 30 C. only, 0.01% moisture was taken up by the explosive.
- Ethylenedinitramine is represented chemically by the formula: 45
- this explosive does not contain suflicient oxygen for complete combustion of the carbon and hydrogen in the compound. It therefore lends itself to admixture with relatively cheap oxidizing agents to provide explosives of various characteristics.
- mixtures of the dinitramine with ammonium perchlorate or potassium chlorate or other active oxidizing agents provide a'series of explosives which possess high brisance and evolve a much greater amount 01 heat and 3,011,678 greater quantity of gas than the dinitramine itself. 7
- An explosive composition including ethylenedinitramine and an oxidizing agent.
- An explosive composition having ethylenedinitramine as an essential constituent.
- An explosive composition comprising ethyl enedinitramine and potassium chlorate.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Air Bags (AREA)
Description
Patented Aug. 20, 1935 UNITED STATES EXPLOSIVE George C. Hale, Dover, N. J.
No, Drawing. Application March 15, 1934, Serial Claims.
(Granted under the act of amended April 30, 1928;
The invention described herein may be manufactured and used by or for the Government for governmental purposes, without the payment to me of any royalty thereon.
5 The subject of this invention is an explosive.
This invention relates to an explosive -compo sition in which ethylenedinitramine is an essential constituent. I have discovered that ethylenedinitramine is an explosive and that it possesses some unusual properties which render it of special interest for various purposes. Outstanding among these properties is its high degree of resistance to detonation by impact or shock as compared to other explosives having equivalent brisance or explosive strength. It is generally recognized that high explosives which have an especially high degree of brisance or shattering effect are commonly more susceptible to detonation by impact or shock than other high explosives having appreciably lower brisance. Thus nitroglycerine, pentaerythritetranitrate, trimethylenetrinitramine, tetranitroaniline and tetryl which are, among the most brisant high explosives which have found military or commercial use are all fairly sensitive to impact or shock. In fact they are so sensitive in this respect that they have not been used as bursting charges for shell or bombs but only considered for use in the form of small charges as boosters or initiators for the main bomb or shell charges. In the form of these small charges they are-not subjected to as rough usage as are the explosives which are handled in large quantity and used as-shell or bomb fillers.
I have found that ethylenedinitramine has brisance or strength comparable to the explosives above mentioned but possesses greater resistance to detonation by shock than any of the explosives mentioned. Actually it corresponds in resistance to shock more nearly to the class of relative insensitive explosives such as picric acid, TNT, etc., which have been used as bursting charges. In the standard droptestit required a 10 inch height of fall of-a 2 kg. weight to cause detonation, this being exactly the same height of fall as was required for picric acid, but the dinitramine showed under test appreciably higher brisance or strength than either picric acid or TNT.
Another important characteristic of ethylenedinitramine is its relatively low ignition temperature. It explodes spontaneously when heated to a temperature of 180 closely to mercury fulmate and nitroglycerine in the ease with which it is detonated by heat. No
C. thus corresponding March 3, 1883, as 370 0. G. 757) other explosive is known to me which has such high resistance to detonation by shock or impact and at the same time is so readily exploded by heat. Picric acid and TNT which, as mentioned above are comparable to the dinitramine in re- 5 sistance to shock, do not explode spontaneously under heat until temperature of approximately 325 C. and 438 C. respectively are reached. Thus the ethylenedinitramine is an explosive which will withstand the shocks incident to transportation, handling, loading, etc., and yet will explode more readily under the action of initiators or detonators than the high explosives commonly used as bursting charges.
Ethylenedinitramine has been found to be substantially insoluble in water only 0.5 gram dissolving in grams of water at 25 C. It has a high degree of stability, withstanding the standard C. Vacuum Stability Test as well as tetryl which has sufiicient stability that it has been widely used in both military and commercial detonators. I have found also that ethylenedinitramine is highly resistant to absorption of moisture from the air as indicated by the fact that when exposed to an atmosphere of 90% relative humidity at a temperature of 30 C. only, 0.01% moisture was taken up by the explosive.
The above highly favorable explosive properties, together with the fact that the raw material, ethylenediamlne, from which the ethylenedinitramine may be derived, is now available commercially, makes possible the utilization of this explosive for various purposes. It may be used to replace tetryl in detonators and boosters or to replace picric acid or TNT in high explosive shell or bombs, etc.; its relative insensitivity to shock, ease of ignition by flame and great explosive strength makes it a favorable substitute for nitroglycerine or nitrocellulose in propellent powders. The unusual combination of the properties of both initiating or detonating agents and -the more insensitive high explosives makes its field of application especially broad.
Ethylenedinitramine is represented chemically by the formula: 45
CH2. N'H. N01
CH2. NH. N02
It is not to be confused with the compound ethylenediaminedinitrate which may be represented chemically by the formula:
As indicated bythe above for ethylenedinitramine this explosive does not contain suflicient oxygen for complete combustion of the carbon and hydrogen in the compound. It therefore lends itself to admixture with relatively cheap oxidizing agents to provide explosives of various characteristics. Thus mixtures of the dinitramine with ammonium perchlorate or potassium chlorate or other active oxidizing agents provide a'series of explosives which possess high brisance and evolve a much greater amount 01 heat and 3,011,678 greater quantity of gas than the dinitramine itself. 7
I claim:
1. A new explosive embodying ethylenedinitramine.
2. An explosive composition including ethylenedinitramine and an oxidizing agent.
3. An explosive composition having ethylenedinitramine as an essential constituent.
. 4. An explosive composition comprlsing -ethyl-' enedinitramine and ammonium perchlorate.
5. An explosive composition comprising ethyl enedinitramine and potassium chlorate.
GEORGE c.
Publications (1)
Publication Number | Publication Date |
---|---|
US2011578A true US2011578A (en) | 1935-08-20 |
Family
ID=3427282
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US2011578D Expired - Lifetime US2011578A (en) | Explosive |
Country Status (1)
Country | Link |
---|---|
US (1) | US2011578A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2462052A (en) * | 1944-12-30 | 1949-02-15 | Honorary Advisory Council Sci | Method of converting secondary amines to nitramines |
US2472105A (en) * | 1943-10-30 | 1949-06-07 | George C Hale | Explosive composition |
US2482090A (en) * | 1944-03-20 | 1949-09-20 | Us Sec War | Method of making a high-density explosive |
US2482091A (en) * | 1944-03-20 | 1949-09-20 | Us Sec War | Method of making a high-density explosive |
US2548880A (en) * | 1948-02-12 | 1951-04-17 | Du Pont | Process of producing cyclonitecontaining explosive |
US2708623A (en) * | 1951-12-29 | 1955-05-17 | Olin Mathieson | Explosive compound, process of making same and a composition thereof |
US2771034A (en) * | 1951-12-29 | 1956-11-20 | Olin Mathieson | Blasting cap |
US3337629A (en) * | 1961-06-08 | 1967-08-22 | Du Pont | 1, 2-bis(difluoroamino)ethylnitramine and process of preparation |
US6354381B1 (en) | 1999-05-28 | 2002-03-12 | Exxonmobil Upstream Research Company | Method of generating heat and vibration in a subterranean hydrocarbon-bearing formation |
US6681857B2 (en) | 2001-01-23 | 2004-01-27 | Exxonmobil Upstream Research Company | Method of generating heat and vibration in a subterranean hydrocarbon-bearing formation |
-
0
- US US2011578D patent/US2011578A/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2472105A (en) * | 1943-10-30 | 1949-06-07 | George C Hale | Explosive composition |
US2482090A (en) * | 1944-03-20 | 1949-09-20 | Us Sec War | Method of making a high-density explosive |
US2482091A (en) * | 1944-03-20 | 1949-09-20 | Us Sec War | Method of making a high-density explosive |
US2462052A (en) * | 1944-12-30 | 1949-02-15 | Honorary Advisory Council Sci | Method of converting secondary amines to nitramines |
US2548880A (en) * | 1948-02-12 | 1951-04-17 | Du Pont | Process of producing cyclonitecontaining explosive |
US2708623A (en) * | 1951-12-29 | 1955-05-17 | Olin Mathieson | Explosive compound, process of making same and a composition thereof |
US2771034A (en) * | 1951-12-29 | 1956-11-20 | Olin Mathieson | Blasting cap |
US3337629A (en) * | 1961-06-08 | 1967-08-22 | Du Pont | 1, 2-bis(difluoroamino)ethylnitramine and process of preparation |
US6354381B1 (en) | 1999-05-28 | 2002-03-12 | Exxonmobil Upstream Research Company | Method of generating heat and vibration in a subterranean hydrocarbon-bearing formation |
US6681857B2 (en) | 2001-01-23 | 2004-01-27 | Exxonmobil Upstream Research Company | Method of generating heat and vibration in a subterranean hydrocarbon-bearing formation |
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