US2004941A - Explosive - Google Patents
Explosive Download PDFInfo
- Publication number
- US2004941A US2004941A US715663A US71566334A US2004941A US 2004941 A US2004941 A US 2004941A US 715663 A US715663 A US 715663A US 71566334 A US71566334 A US 71566334A US 2004941 A US2004941 A US 2004941A
- Authority
- US
- United States
- Prior art keywords
- nitroglycerine
- sensitivity
- explosive
- liquid
- explosives
- 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 15
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 22
- 229960003711 glyceryl trinitrate Drugs 0.000 description 22
- 230000035945 sensitivity Effects 0.000 description 12
- 239000007788 liquid Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 7
- PQSWCVYWEGIBPY-UHFFFAOYSA-N 2,2-dinitroethylbenzene Chemical compound [O-][N+](=O)C([N+]([O-])=O)CC1=CC=CC=C1 PQSWCVYWEGIBPY-UHFFFAOYSA-N 0.000 description 4
- XAWCLWKTUKMCMO-UHFFFAOYSA-N 2-nitroethylbenzene Chemical compound [O-][N+](=O)CCC1=CC=CC=C1 XAWCLWKTUKMCMO-UHFFFAOYSA-N 0.000 description 4
- 239000000020 Nitrocellulose Substances 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 150000002828 nitro derivatives Chemical class 0.000 description 4
- 229920001220 nitrocellulos Polymers 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- DYSXLQBUUOPLBB-UHFFFAOYSA-N 2,3-dinitrotoluene Chemical compound CC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O DYSXLQBUUOPLBB-UHFFFAOYSA-N 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XOXVLXUOMLQTLM-UHFFFAOYSA-N 1-ethyl-2,3,4-trinitrobenzene Chemical compound CCC1=CC=C([N+]([O-])=O)C([N+]([O-])=O)=C1[N+]([O-])=O XOXVLXUOMLQTLM-UHFFFAOYSA-N 0.000 description 2
- -1 dinitro aromatic compounds Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
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
- C06B25/10—Compositions containing a nitrated organic compound the compound being nitroglycerine
- C06B25/12—Compositions containing a nitrated organic compound the compound being nitroglycerine with other nitrated organic compounds
Definitions
- This invention relates to explosives.
- Nitroglycerine has been widely used as a constituent of dynamites and propellent powders.
- One of the main disadvantages in its use for these purposes is its relatively high degree of sensitivity to shock which makes elaborate precautions necessary in the manufacture, transportation and handling of the nitroglycerine as well as many of the explosive compositions containing it. This fact is generally recognized and regulations prohibit the shipment of liquid nitroglycerine. If the nitroglycerine is mixed with nitrocellulose the semiplastic or gelatinized mass resulting may be shipped because the sensitivity of the mixture to shock is much less than that of nitroglycerine and is such that the mixture does not present undue hazard. The mixture is however a powerful explosive and may be used in compounding various high explosives or propellent powders.
- a liquid explosive such as nitroglycerine which does not have the extreme sensitivity of nitroglycerine is highly to be desired.
- Such an explosive might be shipped with on more hazard than the usual high explosives now authorized for shipment, and might be more widely used in compounding various types of high explosives than is the case with nitroglycerine because of restrictions on the transportation of the latter in liquid form. If such a liquid explosive were a solvent or colloiding agent for nitrocellulose it might also be used in compounding propellent powders for various purposes.
- a liquid explosive can be produced by the addition of the nitro derivatives of ethylbenzene to nitroglycerine.
- Dinitroethylbenzene for example, is one of the'few dinitro aromatic compounds known which is liquid in the pure state and which can be produced on a commercial scale.
- nitro aromatic compounds may be added to nitroglycerine to reduce its sensitivity but there are limitations on this as it has been practiced in the past which are not present if the nitro derivatives of ethylbenzene are used; the difference here results from the important fact that the dinitro derivative of ethylbenzene has a low melting point and thus 5 exists as a liquid at ordinary atmospheric temperatures, and the further fact that it is misci-' ble with nitroglycerine in all proportions.
- dinitrotoluene which when pure is a solid, crystalline material, is added to nitroglycerine the sensitivity of the nitroglycerine is reduced to be sure but nitroglycerine will dissolve and hold in solution at room temperature only about 6% of the crystalline dinitrotoluene; it is a slow, tedious and somewhat expensive procedure to obtain even as much as 6% of crystalline dinitrotoluene in solution with nitroglycerine.
- dinitroethylbenzene which is a liquid at room temperature can be added to nitroglycerine in any proportion by simply mixing the one liquid with the other.
Landscapes
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Patented June 18, 1935 EXPLOSIVE George 0. Hale, Dover, N. J.
No Drawing.
4 Claims.
Application March 15, 1934, Serial No. 715,663
(Granted under the act of March 3, 1883, an amended April 30, 1928; 370 0. G. 757) 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.
This invention relates to explosives.
Nitroglycerine has been widely used as a constituent of dynamites and propellent powders. One of the main disadvantages in its use for these purposes is its relatively high degree of sensitivity to shock which makes elaborate precautions necessary in the manufacture, transportation and handling of the nitroglycerine as well as many of the explosive compositions containing it. This fact is generally recognized and regulations prohibit the shipment of liquid nitroglycerine. If the nitroglycerine is mixed with nitrocellulose the semiplastic or gelatinized mass resulting may be shipped because the sensitivity of the mixture to shock is much less than that of nitroglycerine and is such that the mixture does not present undue hazard. The mixture is however a powerful explosive and may be used in compounding various high explosives or propellent powders.
A liquid explosive such as nitroglycerine which does not have the extreme sensitivity of nitroglycerine is highly to be desired. Such an explosive might be shipped with on more hazard than the usual high explosives now authorized for shipment, and might be more widely used in compounding various types of high explosives than is the case with nitroglycerine because of restrictions on the transportation of the latter in liquid form. If such a liquid explosive were a solvent or colloiding agent for nitrocellulose it might also be used in compounding propellent powders for various purposes.
I have found by experimentation that such a liquid explosive can be produced by the addition of the nitro derivatives of ethylbenzene to nitroglycerine. Dinitroethylbenzene, for example, is one of the'few dinitro aromatic compounds known which is liquid in the pure state and which can be produced on a commercial scale. I have found that dinitroethylbenzene or suitable mixtures of it with the mononitroethylbenzene and with the trinitroethylbenzene are miscible with nitroglycerine in all proportions and that these nitro derivatives of ethylbenzene reduce the sensitivity of nitroglycerine to a remarkable degree, the reduction in sensitivity being greater of course as the content of the nitroethylbenzenes is increased. It has long been known that many nitro aromatic compounds may be added to nitroglycerine to reduce its sensitivity but there are limitations on this as it has been practiced in the past which are not present if the nitro derivatives of ethylbenzene are used; the difference here results from the important fact that the dinitro derivative of ethylbenzene has a low melting point and thus 5 exists as a liquid at ordinary atmospheric temperatures, and the further fact that it is misci-' ble with nitroglycerine in all proportions.
If dinitrotoluene, which when pure is a solid, crystalline material, is added to nitroglycerine the sensitivity of the nitroglycerine is reduced to be sure but nitroglycerine will dissolve and hold in solution at room temperature only about 6% of the crystalline dinitrotoluene; it is a slow, tedious and somewhat expensive procedure to obtain even as much as 6% of crystalline dinitrotoluene in solution with nitroglycerine. On the other hand dinitroethylbenzene which is a liquid at room temperature can be added to nitroglycerine in any proportion by simply mixing the one liquid with the other.
Tests made to determine the sensitivity of mix tures of dinitroethylbenzene and nitroglycerine indicate that a mixture containing 25% of the former and 75% of the latter is less sensitive to shock than a nitroglycerine--50% nitrocellulose mixture which is authorized for shipment. In these tests a Pendulum friction machine as described in Bureau of Mines Technical Paper No. 186, the Impact test apparatus as developed by the Bureau of Mines, and other designs of testing machines employed in the industry to determine the sensitivity of explosives were used. Some of the data obtained are as follows: The sensitivity being interpreted by the minimum drop of a 2 kg. weight to cause explosion.
6 ems. 22 cm.
45 The very great reduction in sensitivity of mix- I pier significant reduction in sensitivity is obtained by employing mononitroethylbenzene or trinitroethylbenzene separately or liquid mixtures of the nitro derivatives of ethylbenzene in admixture with nitroglycerine. I have found such mixtures to act as eflicient solvents for nitrocellulose,
the presence of the nitroethylbenzenes. not detracting from the well known efflciency of nitroglycerine in this respect. The opportunity is thus oifered of employing an insensitive liquidexplosive in compounding explosives and propellent powders, which offers much less hazard than nitroglycerine. The practicability of employing the insensitive liquid mixtures alone as explosives is also recognized.
tives of ethylbenzene.
GEORGE C. HALE
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US715663A US2004941A (en) | 1934-03-15 | 1934-03-15 | Explosive |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US715663A US2004941A (en) | 1934-03-15 | 1934-03-15 | Explosive |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2004941A true US2004941A (en) | 1935-06-18 |
Family
ID=24874980
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US715663A Expired - Lifetime US2004941A (en) | 1934-03-15 | 1934-03-15 | Explosive |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2004941A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3000720A (en) * | 1959-04-09 | 1961-09-19 | Baer Maurice | Desensitization of cyclotrimethylenetrinitramine with dinitroethylbenzene |
| US3755021A (en) * | 1971-06-28 | 1973-08-28 | Ici Australia Ltd | Nitric ester explosive composition containing fume reducing agent |
-
1934
- 1934-03-15 US US715663A patent/US2004941A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3000720A (en) * | 1959-04-09 | 1961-09-19 | Baer Maurice | Desensitization of cyclotrimethylenetrinitramine with dinitroethylbenzene |
| US3755021A (en) * | 1971-06-28 | 1973-08-28 | Ici Australia Ltd | Nitric ester explosive composition containing fume reducing agent |
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