US2668102A - Liquid explosives - Google Patents
Liquid explosives Download PDFInfo
- Publication number
- US2668102A US2668102A US246525A US24652551A US2668102A US 2668102 A US2668102 A US 2668102A US 246525 A US246525 A US 246525A US 24652551 A US24652551 A US 24652551A US 2668102 A US2668102 A US 2668102A
- Authority
- US
- United States
- Prior art keywords
- percent
- volume
- nitroglycerine
- methylite
- stabilizer
- 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 claims description 17
- 239000007788 liquid Substances 0.000 title claims description 15
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 claims description 18
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 claims description 13
- 229960003711 glyceryl trinitrate Drugs 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 13
- 239000003381 stabilizer Substances 0.000 claims description 11
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 claims description 9
- 229960001826 dimethylphthalate Drugs 0.000 claims description 9
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 8
- 238000007710 freezing Methods 0.000 description 5
- PZIMIYVOZBTARW-UHFFFAOYSA-N centralite Chemical compound C=1C=CC=CC=1N(CC)C(=O)N(CC)C1=CC=CC=C1 PZIMIYVOZBTARW-UHFFFAOYSA-N 0.000 description 4
- 230000008014 freezing Effects 0.000 description 4
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 3
- UQXKXGWGFRWILX-UHFFFAOYSA-N ethylene glycol dinitrate Chemical compound O=N(=O)OCCON(=O)=O UQXKXGWGFRWILX-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- HZTVIZREFBBQMG-UHFFFAOYSA-N 2-methyl-1,3,5-trinitrobenzene;[3-nitrooxy-2,2-bis(nitrooxymethyl)propyl] nitrate Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O.[O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O HZTVIZREFBBQMG-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 238000005474 detonation Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002023 wood 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
- C06B23/00—Compositions characterised by non-explosive or non-thermic constituents
- C06B23/005—Desensitisers, phlegmatisers
-
- 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
Definitions
- the present invention relates to liquid explosives and is particularly concerned with providing a liquid explosive which among other uses can be employed in a flexible conduit for the demolition of landing obstacles or clearing mine fields during warfare.
- the principal object of the present invention is to provide a low-freezing liquid explosive of high explosive power and moderate viscosity which is relatively insensitive to impact and will remain in good condition over long periods of storage.
- a liquid explosive meeting the aforementioned objects can be produced by phlegmatizing nitroglycerine with dimethylphthalate and including a stabilizer therefor.
- the resulting product is referred to throughout this specification as Methylite.
- the range of proportions of the various ingredients which have been found most suitable for the present purpose consists of 70% to 80% nitroglycerine with from about 19% to 30% dimethylphthalate and a stabilizer in amounts of 0.9% to 1% of the total nitroglycerine mixtureemployed.
- the above percentages represent proportions of the volume of the total liquid explosive.
- a commercial grade nitroglycerine containing a freezing point depressant such as 25%:2% ethylene glycol dinitrate or 30% :L2% diglycerine tetranitrate is suitable for forming the Methylite.
- the ethylene glycol dinitrate i preferred as it is less viscous at low temperatures than the diglycerine tetranitrate.
- ethyl centralite or diphenylamine have been found to be especially suitable for use in the present mixture.
- Either stabilizer should be present in amounts of 0.9% to 1% of the total nitroglycerine present including the aforementioned additives thereto.
- the stabilizer is dissolved in the dimethylphthalate by stirring at 125 F. in an agitated vessel until the solution is complete.
- the resulting solution may then either be placed in containers and stored before use or added directly to the nitroglycerine.
- Methylite Specific examples of acceptable mixtures forming Methylite are as follows:
- the resulting products are low freezing liquids, with freezing temperatures of -4 F. (20 C.)
- Methylite produced according to the present disclosure is insensitive to frictional impact such as being struck a glancing blow and also generally insensitive to direct impact.
- Methylite contained in a Fiberglas hose and backed by air or even wood is not exploded when hit with cal. .50 ball ammunition.
- containers of Methylite dropped from considerable heights onto hard surfaces will not explode as long as the containers do not collapse and pinch the explosive between two parts thereof.
- Such characteristics of the Methylite renders the same safe for normal handling and transportation even under combat conditions.
- a flexible conduit containing Methylite can be exploded by employing a two pound or more external booster of cast Pentolite, Tetrytol or the like for initiation of the Methylite in the conduit.
- a liquid explosive composition adapted to operation in a flexible conduit comprising to percent by volume of nitroglycerine, and from 19 to 30 percent by volume of dimethylphthalate.
- a liquid explosive composition adapted to operation in a flexible conduit comprising 70 to 80 percent by volume of nitroglycerine, from 19 to 30 percent by volume of dimethylphthalate and from 0.7 to 1 percent of a stabilizer.
- a liquid explosive composition adapted to operation in a flexible conduit comprising from 70 to 80 percent by volume of nitroglycerine, from 19 to 30 percent by volume of dimethylphthalate, and from 0.7 to 1 percent by volume of a stabilizer selected from the group consisting of ethyl centralite and diphenylamine.
- a liquid explosive composition adapted to operation in a flexible conduit comprising 70 to 80 percent by volume of nitroglycerine, 19. to 30 percent by volume of dimethylphthalate, 0.7 to 1 percent of a stabilizer selected from the group 3 4 consisting of ethyl centralite and diphenylamine, References Cited in the file of this patent and 25-12% by volume of a. freezing point de- UNITED STATES PATENTS pressant selected from the group consistmg of ethylene glycol dinitrate and diglycerine tetra- Number Name Date nitrate 5 1,205,516 Cos by Nov. 21, 1916 5.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
Patented Feb. 2, 1954 UNITED LIQUID EXPLOSIVES No Drawing. Application September 13, 1951, Serial No. 246,525
6 Claims.
The present invention relates to liquid explosives and is particularly concerned with providing a liquid explosive which among other uses can be employed in a flexible conduit for the demolition of landing obstacles or clearing mine fields during warfare.
The principal object of the present invention is to provide a low-freezing liquid explosive of high explosive power and moderate viscosity which is relatively insensitive to impact and will remain in good condition over long periods of storage.
It has been discovered that a liquid explosive meeting the aforementioned objects can be produced by phlegmatizing nitroglycerine with dimethylphthalate and including a stabilizer therefor. The resulting product is referred to throughout this specification as Methylite. The range of proportions of the various ingredients which have been found most suitable for the present purpose consists of 70% to 80% nitroglycerine with from about 19% to 30% dimethylphthalate and a stabilizer in amounts of 0.9% to 1% of the total nitroglycerine mixtureemployed. The above percentages represent proportions of the volume of the total liquid explosive.
A commercial grade nitroglycerine containing a freezing point depressant such as 25%:2% ethylene glycol dinitrate or 30% :L2% diglycerine tetranitrate is suitable for forming the Methylite.
Of these additives the ethylene glycol dinitrate i preferred as it is less viscous at low temperatures than the diglycerine tetranitrate.
As examples of stabilizers, ethyl centralite or diphenylamine have been found to be especially suitable for use in the present mixture. Either stabilizer should be present in amounts of 0.9% to 1% of the total nitroglycerine present including the aforementioned additives thereto.
In preparing the Methylite, the stabilizer is dissolved in the dimethylphthalate by stirring at 125 F. in an agitated vessel until the solution is complete. The resulting solution may then either be placed in containers and stored before use or added directly to the nitroglycerine.
Specific examples of acceptable mixtures forming Methylite are as follows:
The resulting products are low freezing liquids, with freezing temperatures of -4 F. (20 C.)
2 for mixture No.2 and -22 F. (-30 C.) for mixture No. 1. They have a moderate viscosity and high explosive power with a detonation velocity of 7000-7300 M./Sec. Solution No. 1 is designed to propagate an explosion in diameters as low as 1" when unconfined and solution No. 2 in columns of 3" or larger. The Methylite so produced can be stored over a period of many years and notably longer than nitroglycerine, without decomposition.
Methylite produced according to the present disclosure is insensitive to frictional impact such as being struck a glancing blow and also generally insensitive to direct impact. For instance Methylite contained in a Fiberglas hose and backed by air or even wood is not exploded when hit with cal. .50 ball ammunition. Similarly containers of Methylite dropped from considerable heights onto hard surfaces will not explode as long as the containers do not collapse and pinch the explosive between two parts thereof. Such characteristics of the Methylite renders the same safe for normal handling and transportation even under combat conditions.
A flexible conduit containing Methylite can be exploded by employing a two pound or more external booster of cast Pentolite, Tetrytol or the like for initiation of the Methylite in the conduit.
It is to be understood that other proportions of the ingredients can be used to form a liquid explosive besides those described herein but the proportions given are preferred mixtures having all Of the characteristics desired.
We claim:
1. A liquid explosive composition adapted to operation in a flexible conduit comprising to percent by volume of nitroglycerine, and from 19 to 30 percent by volume of dimethylphthalate.
2. A liquid explosive composition adapted to operation in a flexible conduit comprising 70 to 80 percent by volume of nitroglycerine, from 19 to 30 percent by volume of dimethylphthalate and from 0.7 to 1 percent of a stabilizer.
3. A liquid explosive composition adapted to operation in a flexible conduit comprising from 70 to 80 percent by volume of nitroglycerine, from 19 to 30 percent by volume of dimethylphthalate, and from 0.7 to 1 percent by volume of a stabilizer selected from the group consisting of ethyl centralite and diphenylamine.
4. A liquid explosive composition adapted to operation in a flexible conduit comprising 70 to 80 percent by volume of nitroglycerine, 19. to 30 percent by volume of dimethylphthalate, 0.7 to 1 percent of a stabilizer selected from the group 3 4 consisting of ethyl centralite and diphenylamine, References Cited in the file of this patent and 25-12% by volume of a. freezing point de- UNITED STATES PATENTS pressant selected from the group consistmg of ethylene glycol dinitrate and diglycerine tetra- Number Name Date nitrate 5 1,205,516 Cos by Nov. 21, 1916 5. A composition according to claim 3 wherein 1,836,563 wlghtsman 15, 1931 the stabilizer is ethyl centralite. 1,999,828 wlggam 30, 1935 6. A composition according to claim 3 wherein 2,003,839 Wagner July 1935 the stabilizer is diphenylamine. 0 FOREIGN PATENTS HOWARD J" FISHER Number Country Date DUNCAN P. MACDOUGALLV GEORGE B. KISTIAKOWSKY. 621,685 Great Brltam Apr. 14, 1949
Claims (2)
1. A LIQUID EXPLOSIVE COMPOSITION ADAPTED TO OPERATION IN A FLEXIBLE CONDUIT COMPRISING 70 TO 80 PERCENT BY VOLUME OF NITROGLYCERINE, AND FROM 19 TO 30 PERCENT BY VOLUME OF DIMETHYLPHTHALATE.
2. A LIQUID EXPLOSIVE COMPOSITION ADAPTED TO OPERATION IN A FLEXIBLE CONDUIT COMPRISING 70 TO 80 PERCENT BY VOLUME OF NITROGLYCERINE, FROM 19 TO 30 PERCENT BY VOLUME OF DIMETHYLPHTHALATE AND FROM 0.7 TO 1 PERCENT OF A STABILIZER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US246525A US2668102A (en) | 1951-09-13 | 1951-09-13 | Liquid explosives |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US246525A US2668102A (en) | 1951-09-13 | 1951-09-13 | Liquid explosives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2668102A true US2668102A (en) | 1954-02-02 |
Family
ID=22931051
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US246525A Expired - Lifetime US2668102A (en) | 1951-09-13 | 1951-09-13 | Liquid explosives |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2668102A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3116188A (en) * | 1960-08-03 | 1963-12-31 | Theodore D Austin | Desensitization of liquid explosives |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1205516A (en) * | 1916-07-08 | 1916-11-21 | Walter Cosby | Explosive containing nitroglycerin. |
| US1836568A (en) * | 1927-12-20 | 1931-12-15 | Du Pont | Nitrated glucoside explosive and process of producing the same |
| US1999828A (en) * | 1932-11-28 | 1935-04-30 | Hercules Powder Co Ltd | Nitrated polyhydric alcohol emulsion and process of producing |
| US2008889A (en) * | 1930-12-08 | 1935-07-23 | Western Cartridge Co | Propellant powder |
| GB621685A (en) * | 1946-03-20 | 1949-04-14 | Hercules Powder Co Ltd | Smokeless powder |
-
1951
- 1951-09-13 US US246525A patent/US2668102A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1205516A (en) * | 1916-07-08 | 1916-11-21 | Walter Cosby | Explosive containing nitroglycerin. |
| US1836568A (en) * | 1927-12-20 | 1931-12-15 | Du Pont | Nitrated glucoside explosive and process of producing the same |
| US2008889A (en) * | 1930-12-08 | 1935-07-23 | Western Cartridge Co | Propellant powder |
| US1999828A (en) * | 1932-11-28 | 1935-04-30 | Hercules Powder Co Ltd | Nitrated polyhydric alcohol emulsion and process of producing |
| GB621685A (en) * | 1946-03-20 | 1949-04-14 | Hercules Powder Co Ltd | Smokeless powder |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3116188A (en) * | 1960-08-03 | 1963-12-31 | Theodore D Austin | Desensitization of liquid explosives |
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