US1045012A - Explosive. - Google Patents
Explosive. Download PDFInfo
- Publication number
- US1045012A US1045012A US60658911A US1911606589A US1045012A US 1045012 A US1045012 A US 1045012A US 60658911 A US60658911 A US 60658911A US 1911606589 A US1911606589 A US 1911606589A US 1045012 A US1045012 A US 1045012A
- Authority
- US
- United States
- Prior art keywords
- nitro
- explosive
- tetra
- anilin
- instance
- 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 12
- 239000000203 mixture Substances 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 3
- 239000003610 charcoal Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 230000037452 priming Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- SPSSULHKWOKEEL-UHFFFAOYSA-N 2,4,6-trinitrotoluene Chemical compound CC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O SPSSULHKWOKEEL-UHFFFAOYSA-N 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical class NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- MHWLNQBTOIYJJP-UHFFFAOYSA-N mercury difulminate Chemical compound [O-][N+]#C[Hg]C#[N+][O-] MHWLNQBTOIYJJP-UHFFFAOYSA-N 0.000 description 2
- 150000002828 nitro derivatives Chemical class 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 description 1
- 241000251729 Elasmobranchii Species 0.000 description 1
- USXDFAGDIOXNML-UHFFFAOYSA-N Fulminate Chemical compound [O-][N+]#[C-] USXDFAGDIOXNML-UHFFFAOYSA-N 0.000 description 1
- RLDTYDPXNLFEIR-UHFFFAOYSA-N N-(5-methyl-2,3,4-trinitrophenyl)-N-nitronitramide Chemical compound CC=1C(=C(C(=C(N([N+](=O)[O-])[N+](=O)[O-])C1)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-] RLDTYDPXNLFEIR-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 241001197925 Theila Species 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- BYNPVFHVZRNRQD-UHFFFAOYSA-N acetic acid;benzene Chemical compound CC(O)=O.C1=CC=CC=C1 BYNPVFHVZRNRQD-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- DVARTQFDIMZBAA-UHFFFAOYSA-O ammonium nitrate Chemical compound [NH4+].[O-][N+]([O-])=O DVARTQFDIMZBAA-UHFFFAOYSA-O 0.000 description 1
- -1 aromatic nitro compounds Chemical class 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000003721 gunpowder Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- 229940079938 nitrocellulose Drugs 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000015 trinitrotoluene Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene 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
- C06B37/00—Compositions containing a metal fulminate
- C06B37/02—Compositions containing a metal fulminate with a nitrated organic compound or an inorganic oxygen-halogen salt
Definitions
- ibustible bodies such as napthalene or fication.
- This invention relates to the use oi s, nitroderivative of anilin, viz., tetrafinin'oanilin, as an explosive or as an ingredient in the manufacture of explosives.
- tetra-nitro-anilin in spite of its high percentage of nitrogen and oxygen, tetra-nitro-anilin has a comparatively high resistance to heat and me chanical influences, and its manufacture is simple and cheap. It is therefore eminently suitable as an explosive or in the manufacture of explosives.
- Tetran1tro-an11m 1s a very powerful exlosive, and may be fired in a known'manner, for instance by an ordinary detonator; it may therefore be used for instance as an Application m s Febrpary ,;1911. Serial No. mm,
- Tetra-nitro-ani'li-n and its mentioned above may be employed together with other nit-r0 compounds, or Withoxidizing bodies, such as (perchlorates, and com aluminium powder or other materials, which have been or may be used in combination with other nitro compounds, for instance by simply mixing or melting them together, or by causing then-r to unite by means of a suitable solvent or a colloid solution,-such as nitro-cellulose in acetone, with or without the aid of pressure. They may also be used in detonating or priming compositions in conjunction with priming substances such as fulminate of mercury or nitrids, as is the case, for instance, with trinitrotoluene and tetra-nitro-methyl-anilin.
- priming substances such as fulminate of mercury or nitrids
- compositions These proportions may be varied and a part or the Whole of the charcoal may be 'reor other combustible bodies.
- the tetranitro-anilin and the ila'phthalone may be melted together.
- the ammonium-nitrate- ' may be replaced by a' suitable quantity of another oxygen earner.
- Tetra-nitroeanilin in u 13parts.
- Charcoal 6' Ammonium nitrate 81 placed by a suitable quantity of naphthalene composition may be prepared from this mixture as follows A mixture consisting of tetra-nitro-anilin and dinitro-benzene,
- Tetra-nitro-anilin is; ayellotv crystalline product or powder having a specific gravity of about 1.8 and melting at about 210? with decomposition, .It is easily soluble acetone, less soluble in acetic acid; benzene and chloroform and almost insoluble in cold water. It can be recrystallized, for instancefrom glacial acetic acid, or from nitl'b-benzene or xylene, andis characterized by the remarkable facility with which-its nitro group in the 3-position may be replaced by, other groups. Thus the compound can in acetonic solution, for instance, be quantitatively transformed into trijnitro-metaamino-phenol melting at 174to 175 C.
- nitro group in the 3-position can also be replaced by numerous other radicals, for instance by amins; the amino gr0up"f'can equally be replaced, li'ough not so easily.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
immmann aacauns rrunscnnm, or rnnn'r, l ng fiatcntedfiov; 19, I912.
To all whom it may concern:
Be it known that I, Benzene .Jeeonss FLtinsoHnnr, doctor of philosophy androsearch chemist, by birth a German subject, but having applied for naturalization as a British subject, residing at Fleet, Hampshire, England, have invented certain new and useful Improvements Relating to 1213- plosives, of which the following is a Speei-.
' ibustible bodies, such as napthalene or fication.
This invention, relates to the use oi s, nitroderivative of anilin, viz., tetrafinin'oanilin, as an explosive or as an ingredient in the manufacture of explosives.
In comparison with other aromatic nitro compounds, hitherto employed in the manufacture of explosive compositions, suchas trinitro-toluol, this new compound possesses a considerably greater explosivepower, as shown by careful experiments. Moreover,
in spite of its high percentage of nitrogen and oxygen, tetra-nitro-anilin has a comparatively high resistance to heat and me chanical influences, and its manufacture is simple and cheap. It is therefore eminently suitable as an explosive or in the manufacture of explosives.
Besides tetra-nitro-anilin, those derivatives of the same, Which contain substituents in the amino group, for instance methylnitro-tetra-nitro-anilin,
l/ w hltl uo/Vvmz on N/ \m j v which melts at about 145 0., are also suitable for use as or m the manufacture of explosives.
Tetran1tro-an11m 1s a very powerful exlosive, and may be fired in a known'manner, for instance by an ordinary detonator; it may therefore be used for instance as an Application m s Febrpary ,;1911. Serial No. mm,
for shells, torpedoes and similar objects, or for the manufacture of gun-powder, as is the case, for-instance with gun-cotton and scan .other known nitro compounds.
, Tetra-nitro-ani'li-n and its mentioned above may be employed together with other nit-r0 compounds, or Withoxidizing bodies, such as (perchlorates, and com aluminium powder or other materials, which have been or may be used in combination with other nitro compounds, for instance by simply mixing or melting them together, or by causing then-r to unite by means of a suitable solvent or a colloid solution,-such as nitro-cellulose in acetone, with or without the aid of pressure. They may also be used in detonating or priming compositions in conjunction with priming substances such as fulminate of mercury or nitrids, as is the case, for instance, with trinitrotoluene and tetra-nitro-methyl-anilin.
The following are examples of useful compositions These proportions may be varied and a part or the Whole of the charcoal may be 'reor other combustible bodies. The tetranitro-anilin and the ila'phthalone may be melted together. "The ammonium-nitrate- 'may be replaced by a' suitable quantity of another oxygen earner.
Ewamp le II.
explosive charge for blasting purposes, also derivatives Et omple I. V
Tetra-nitroeanilin"in u 13parts. Charcoal 6' Ammonium nitrate 81 placed by a suitable quantity of naphthalene composition may be prepared from this mixture as follows A mixture consisting of tetra-nitro-anilin and dinitro-benzene,
as described above a- '7 parts. Charcoal 6 1 Ammonium-nitrate 87 Y Q 100' Eat-ample H I Fulminate of mercury composition (containing 10 to 20% of KGlO, and 9080 of fulmmate) about 25 parts. Tetra-nitro-ahilin, about 75 i f 100 IV. Fulminate of merohry composition (containing 10 to 20% KClO -and 90-80 of fulmmate) about 25pa-rts. Methyl-nitro tetra-nitro-an1l1n,
v v No:
' awaits NO/ NO: 7
Examples III and Wrente'iouemaaeig compositions in which the ingredientsare.
usually not mixed together, but placedone above the other.
Tetra-nitro-anilin is; ayellotv crystalline product or powder having a specific gravity of about 1.8 and melting at about 210? with decomposition, .It is easily soluble acetone, less soluble in acetic acid; benzene and chloroform and almost insoluble in cold water. It can be recrystallized, for instancefrom glacial acetic acid, or from nitl'b-benzene or xylene, andis characterized by the remarkable facility with which-its nitro group in the 3-position may be replaced by, other groups. Thus the compound can in acetonic solution, for instance, be quantitatively transformed into trijnitro-metaamino-phenol melting at 174to 175 C. by treatment with anaqueous solution of so dium-acetate at ordinary'temperature. The nitro group in the 3-position can also be replaced by numerous other radicals, for instance by amins; the amino gr0up"f'can equally be replaced, li'ough not so easily.
The chemical cons ltlltlOIl may be'indie cated by the formula:
lowsz+1 part of meta-nitro-anil-in and parts of sodium nitrate are dissolved in36 parts'of concentrated sulfuric acid, the mass is then heated to about C. to 90 C. and external cooling is applied, to prevent the temperature from rising, When the-reaction 2 100 C. for a few minutesfith'en allowed to cool, and. thetetra nitroanilin separated by -.'J'Z"|I filtration. r
stobdtha'tin the claims appended hereto the eizpression; an explosive containing is to"- V be mterpretedto mean-an explosive com- In'view of the foregoing it is to be under-' has subsided, 'the mass is "heated further to i prising at least one constituent in addition 7 to the tetra-nitrovanilin. i What I claim is '1. An explosive containing a ,"offanilin havingrfourynitro groups-in the substantially as described.
w positions 2, 3, and Sin the benzene. nucleus,
"anilin of the constitution I I NO:
NO/ No,
substantially as described.
3. A detonating charge containing-tetranitro-anilin in addition to a priming substance, substantially as described. 3
Intestimony'whereof I have hereunto set derivative 1' 2. An explosive; containing tetrainitroamy hand in presence of two subscribing wit- BERNHARD JACQUES FLllRSCHEIM.
Witnesses:
J. Wm, H. D. JAMIESON.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60658911A US1045012A (en) | 1911-02-04 | 1911-02-04 | Explosive. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60658911A US1045012A (en) | 1911-02-04 | 1911-02-04 | Explosive. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1045012A true US1045012A (en) | 1912-11-19 |
Family
ID=3113286
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US60658911A Expired - Lifetime US1045012A (en) | 1911-02-04 | 1911-02-04 | Explosive. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1045012A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2487906A (en) * | 1946-07-08 | 1949-11-15 | Atlas Powder Co | Ignition composition |
| US2908560A (en) * | 1953-04-13 | 1959-10-13 | Dynamit Ag Vormals Alfred Nobe | Non-caking water-resistant explosive of the ammonium nitrate type |
| DE1301271B (en) * | 1965-03-01 | 1969-08-14 | Delegation Ministerielle Pour | Castable explosive mixture on the basis of hexogen and / or octogen and process for its production |
| DE1646307B1 (en) * | 1967-09-28 | 1971-06-24 | Wasagchemie Ag | Meltable explosives mixture |
-
1911
- 1911-02-04 US US60658911A patent/US1045012A/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2487906A (en) * | 1946-07-08 | 1949-11-15 | Atlas Powder Co | Ignition composition |
| US2908560A (en) * | 1953-04-13 | 1959-10-13 | Dynamit Ag Vormals Alfred Nobe | Non-caking water-resistant explosive of the ammonium nitrate type |
| DE1301271B (en) * | 1965-03-01 | 1969-08-14 | Delegation Ministerielle Pour | Castable explosive mixture on the basis of hexogen and / or octogen and process for its production |
| DE1646307B1 (en) * | 1967-09-28 | 1971-06-24 | Wasagchemie Ag | Meltable explosives mixture |
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