US20080006167A1 - Blast effect charge - Google Patents
Blast effect charge Download PDFInfo
- Publication number
- US20080006167A1 US20080006167A1 US11/770,800 US77080007A US2008006167A1 US 20080006167 A1 US20080006167 A1 US 20080006167A1 US 77080007 A US77080007 A US 77080007A US 2008006167 A1 US2008006167 A1 US 2008006167A1
- Authority
- US
- United States
- Prior art keywords
- blast effect
- effect charge
- explosive
- binding agent
- red phosphorous
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B39/00—Compositions containing free phosphorus or a binary compound of phosphorus, except with oxygen
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
- C06B21/0033—Shaping the mixture
- C06B21/005—By a process involving melting at least part of the ingredients
-
- 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
- C06B25/34—Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine
Definitions
- the present invention relates to a high-explosive blast effect charge.
- HE blast effect charges are typically composed of mixtures of explosives with metallic fuels such as boron, silicon, aluminium, titanium, zirconium, magnesium or mixtures, metal-rich compounds, or alloys of these metals.
- One object of the present invention is therefore to provide a high-explosive blast effect charge which avoids the abovementioned problems with conventional blast effect charges.
- One particular aim is to produce a higher performance blast effect charge, that is to say faster combustion, which is as complete as possible, in enclosed areas.
- the blast effect charge proposed according to the present invention is composed of red phosphorous or a compound containing red phosphorous, an explosive and a binding agent.
- the blast effect charge is thus highly explosive, burns more quickly and completely than conventional blast effect charges based on metal, and thus achieves a very high pressure volume work.
- the binding agent for the blast effect charge can optionally be an inert binding agent or an explosive, such as TNT or TATB.
- the molecular P/O ratio of the blast effect charge may be either ⁇ 2/5 or else ⁇ 2/5.
- the present invention solves the problems described in the introduction of conventional blast effect charges based on metal, by the use of red phosphorous.
- red phosphorous When red phosphorous is ignited at atmospheric pressure, then it burns slowly in the region of 0.1 mm/s. Oxygen-unbalanced pyrotechnic charges based on red phosphorous in contrast produce combustion rates of 1/2 mm/s. When charges such as these are enclosed, the combustion after ignition is even explosive.
- Mixtures comprising the system octogen (explosive with the overall formula C 4 H 8 N 8 O 8 , cyclotetramethylene tetranitramine, also referred to as Homocyclonite or HMX (High Melting Explosive)/hydroxyl-terminated polybutadiene (HTPB, use as a fuel and a binding agent) and red phosphorous (RP) produce detonation rates which are higher than those of pure HMX.
- HMX High Melting Explosive
- HTPB hydroxyl-terminated polybutadiene
- RP red phosphorous
- an explosive such as TNT or TATB can also be used as the binding agent, instead of the non-explosive HTPB, which is difficult to ignite.
- the molecular P/O ratio of the blast effect charge may be not only ⁇ 2/5 but also ⁇ 2/5, depending on its composition.
- red phosphorous or of compounds containing red phosphorous in the blast effect charge according to the invention results in a high pressure exponent n in Dahlle's Law as mentioned initially, which results in faster combustion in enclosed areas.
- the resultant oxide is in this case highly volatile (for example from about 250° C.), which leads to a complete, or at least virtually complete, reaction of the effect charge, while at the same time making a contribution to the pressure-volume work.
- the blast effect charge also requires a smaller proportion of expensive nitramines such as HMX and the like than conventional systems.
Abstract
Description
- 1. Field of the Invention
- The present invention relates to a high-explosive blast effect charge.
- Conventional high-explosive (HE) blast effect charges are typically composed of mixtures of explosives with metallic fuels such as boron, silicon, aluminium, titanium, zirconium, magnesium or mixtures, metal-rich compounds, or alloys of these metals.
- 2. Discussion of the Prior Art
- One inherent disadvantage of the use of metals in binary and uniform charges of this type is the fact that the combustion of metal particles is in general influenced only insignificantly by the atmospheric pressure. This means that the pressure exponent n in Vielle's Law r=a.pn is only very small. Furthermore, metals in principle suffer from the defect that the oxide layers which adhere to them prevent rapid combustion. In particular, boron, which is calorifically so advantageous, with a volume-related combustion enthalpy of 138 MJ/dm3 is not completely involved in a reaction owing to the inherent B2O3 layer, irrespective of whether this is in the detonation reaction zone or during subsequent combustion.
- The problems of conventional blast effect charges based on metal are therefore:
- a small pressure exponent n of the metals used and thus scarcely any increase in the combustion rate in enclosed areas, and
- incomplete reaction of the metals as a result of oxide layers.
- One object of the present invention is therefore to provide a high-explosive blast effect charge which avoids the abovementioned problems with conventional blast effect charges. One particular aim is to produce a higher performance blast effect charge, that is to say faster combustion, which is as complete as possible, in enclosed areas.
- The blast effect charge proposed according to the present invention is composed of red phosphorous or a compound containing red phosphorous, an explosive and a binding agent.
- The advantages of a blast effect charge such as this containing red phosphorous are, in particular,
- a high pressure exponent n and thus faster combustion in enclosed areas, and
- high volatility of the resultant oxide, and thus a contribution to the pressure volume work.
- The blast effect charge is thus highly explosive, burns more quickly and completely than conventional blast effect charges based on metal, and thus achieves a very high pressure volume work.
- The binding agent for the blast effect charge can optionally be an inert binding agent or an explosive, such as TNT or TATB.
- The molecular P/O ratio of the blast effect charge may be either ≦2/5 or else ≧2/5.
- The above and further features and advantages of the invention will be understood better from the following description of one preferred, non-restrictive, exemplary embodiment.
- The present invention solves the problems described in the introduction of conventional blast effect charges based on metal, by the use of red phosphorous.
- When red phosphorous is ignited at atmospheric pressure, then it burns slowly in the region of 0.1 mm/s. Oxygen-unbalanced pyrotechnic charges based on red phosphorous in contrast produce combustion rates of 1/2 mm/s. When charges such as these are enclosed, the combustion after ignition is even explosive.
- Mixtures comprising the system octogen (explosive with the overall formula C4H8N8O8, cyclotetramethylene tetranitramine, also referred to as Homocyclonite or HMX (High Melting Explosive)/hydroxyl-terminated polybutadiene (HTPB, use as a fuel and a binding agent) and red phosphorous (RP) produce detonation rates which are higher than those of pure HMX. Thus, for example, the ternary system HMX/HTPB/RP with a mixture ratio of 68/12/20 produces a detonation rate of approximately 11 100 m/s and a Chapman-Jouget pressure of not less than 55 GPa.
- However, the invention is of course not just restricted to blast effect charges using the above ternary system HMX/HTPB/RP.
- For example, an explosive such as TNT or TATB can also be used as the binding agent, instead of the non-explosive HTPB, which is difficult to ignite.
- Furthermore, the molecular P/O ratio of the blast effect charge may be not only ≦2/5 but also ≧2/5, depending on its composition.
- The use of red phosphorous or of compounds containing red phosphorous in the blast effect charge according to the invention results in a high pressure exponent n in Vielle's Law as mentioned initially, which results in faster combustion in enclosed areas. Furthermore, the resultant oxide is in this case highly volatile (for example from about 250° C.), which leads to a complete, or at least virtually complete, reaction of the effect charge, while at the same time making a contribution to the pressure-volume work. As is evident from the above description, the blast effect charge also requires a smaller proportion of expensive nitramines such as HMX and the like than conventional systems.
Claims (5)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102006030678.3 | 2006-07-04 | ||
DE102006030678A DE102006030678B4 (en) | 2006-07-04 | 2006-07-04 | explosive charge |
Publications (1)
Publication Number | Publication Date |
---|---|
US20080006167A1 true US20080006167A1 (en) | 2008-01-10 |
Family
ID=38331717
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/770,800 Abandoned US20080006167A1 (en) | 2006-07-04 | 2007-06-29 | Blast effect charge |
Country Status (5)
Country | Link |
---|---|
US (1) | US20080006167A1 (en) |
EP (1) | EP1876160B1 (en) |
DE (2) | DE102006030678B4 (en) |
NO (1) | NO20073027L (en) |
ZA (1) | ZA200705369B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2479821C2 (en) * | 2010-11-23 | 2013-04-20 | Федеральное государственное унитарное предприятие "Российский федеральный ядерный центр - Всероссийский научно-исследовательский институт технической физики имени академика Е.И. Забабахина" | Apparatus for forming compact element |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102008036649A1 (en) | 2008-08-06 | 2010-02-18 | Diehl Bgt Defence Gmbh & Co. Kg | Active agent for selectively causing detonation or deflagration |
DE102010005923B4 (en) | 2009-12-23 | 2016-03-24 | Diehl Bgt Defence Gmbh & Co. Kg | Pressable insensitive explosive mixture |
DE102010022982B3 (en) | 2010-06-08 | 2013-09-26 | Rheinmetall Waffe Munition Gmbh | Pressure-increasing explosive charge and ammunition containing this charge |
DE102010022983A1 (en) | 2010-06-08 | 2011-12-08 | Rheinmetall Waffe Munition Gmbh | Two-shell explosive charge |
DE102018113345B4 (en) * | 2018-06-05 | 2021-12-23 | Rheinmetall Waffe Munition Gmbh | Explosives formulation |
Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2970900A (en) * | 1949-06-24 | 1961-02-07 | Olin Mathieson | Priming composition |
US3733224A (en) * | 1972-08-24 | 1973-05-15 | G Floyd | Explosive composition containing phosphorus and particulate coffee |
US3786751A (en) * | 1972-02-15 | 1974-01-22 | Us Army | Pressure sensitive mine insensitive to water deactivation |
US3904451A (en) * | 1973-11-28 | 1975-09-09 | Westinghouse Electric Corp | Method for preparing primer for percussion-ignitable flash lamp |
US4361450A (en) * | 1975-06-02 | 1982-11-30 | Thiokol Corporation | Plastic bonded explosive compositions |
US5352829A (en) * | 1993-04-02 | 1994-10-04 | The United States Of America As Represented By The Secretary Of The Navy | Spiro(N,N'-dinitroethylenediamino)cyclotriphosphazenes |
US20040112487A1 (en) * | 2002-05-15 | 2004-06-17 | Miskelly Hermann L. | Solid propellant formulations and methods and devices employing the same for the destruction of airborne biological and/or chemical agents |
US20040216822A1 (en) * | 2001-07-03 | 2004-11-04 | Heinz Hofmann | Process for the production of a pressed insensitive explosive mixture |
US20050230019A1 (en) * | 1999-12-22 | 2005-10-20 | Doll Daniel W | Reduced sensitivity melt-cast explosives |
US6969434B1 (en) * | 2002-12-23 | 2005-11-29 | The United States Of America As Represented By The Secretary Of The Navy | Castable thermobaric explosive formulations |
US20060060273A1 (en) * | 2004-05-06 | 2006-03-23 | Kjell-Tore Smith | Pressable explosive composition |
US20060225599A1 (en) * | 2004-11-22 | 2006-10-12 | Giat Industries | Piece of ammunition or ammunition component comprising a structural energetic material |
US20080099112A1 (en) * | 2001-06-27 | 2008-05-01 | Doll Daniel W | Reduced sensitivity melt-pourable Tritonal replacements |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT172937B (en) * | 1948-06-26 | 1952-10-25 | August Dipl Ing Nuhsbaum | Detonator |
CH317908A (en) * | 1951-07-12 | 1956-12-15 | Hispano Suiza S A Tanger | Process for the manufacture of explosive devices |
DE1122424B (en) * | 1960-12-09 | 1962-01-18 | Olin Mathieson | Ignition mixture |
WO2004069771A1 (en) * | 2003-02-05 | 2004-08-19 | Metlite Alloys Gauteng (Pty) Ltd. | Explosive composition |
FR2868774B1 (en) * | 2004-04-07 | 2007-01-12 | Giat Ind Sa | EXPLOSIVE COMPOSITION |
-
2006
- 2006-07-04 DE DE102006030678A patent/DE102006030678B4/en not_active Expired - Fee Related
-
2007
- 2007-06-13 NO NO20073027A patent/NO20073027L/en not_active Application Discontinuation
- 2007-06-29 US US11/770,800 patent/US20080006167A1/en not_active Abandoned
- 2007-06-30 DE DE502007001607T patent/DE502007001607D1/en active Active
- 2007-06-30 EP EP07012879A patent/EP1876160B1/en not_active Expired - Fee Related
- 2007-07-02 ZA ZA200705369A patent/ZA200705369B/en unknown
Patent Citations (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2970900A (en) * | 1949-06-24 | 1961-02-07 | Olin Mathieson | Priming composition |
US3786751A (en) * | 1972-02-15 | 1974-01-22 | Us Army | Pressure sensitive mine insensitive to water deactivation |
US3733224A (en) * | 1972-08-24 | 1973-05-15 | G Floyd | Explosive composition containing phosphorus and particulate coffee |
US3904451A (en) * | 1973-11-28 | 1975-09-09 | Westinghouse Electric Corp | Method for preparing primer for percussion-ignitable flash lamp |
US4361450A (en) * | 1975-06-02 | 1982-11-30 | Thiokol Corporation | Plastic bonded explosive compositions |
US5352829A (en) * | 1993-04-02 | 1994-10-04 | The United States Of America As Represented By The Secretary Of The Navy | Spiro(N,N'-dinitroethylenediamino)cyclotriphosphazenes |
US20050230019A1 (en) * | 1999-12-22 | 2005-10-20 | Doll Daniel W | Reduced sensitivity melt-cast explosives |
US20080099112A1 (en) * | 2001-06-27 | 2008-05-01 | Doll Daniel W | Reduced sensitivity melt-pourable Tritonal replacements |
US20040216822A1 (en) * | 2001-07-03 | 2004-11-04 | Heinz Hofmann | Process for the production of a pressed insensitive explosive mixture |
US20040112487A1 (en) * | 2002-05-15 | 2004-06-17 | Miskelly Hermann L. | Solid propellant formulations and methods and devices employing the same for the destruction of airborne biological and/or chemical agents |
US6969434B1 (en) * | 2002-12-23 | 2005-11-29 | The United States Of America As Represented By The Secretary Of The Navy | Castable thermobaric explosive formulations |
US20060060273A1 (en) * | 2004-05-06 | 2006-03-23 | Kjell-Tore Smith | Pressable explosive composition |
US20060225599A1 (en) * | 2004-11-22 | 2006-10-12 | Giat Industries | Piece of ammunition or ammunition component comprising a structural energetic material |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2479821C2 (en) * | 2010-11-23 | 2013-04-20 | Федеральное государственное унитарное предприятие "Российский федеральный ядерный центр - Всероссийский научно-исследовательский институт технической физики имени академика Е.И. Забабахина" | Apparatus for forming compact element |
Also Published As
Publication number | Publication date |
---|---|
EP1876160A1 (en) | 2008-01-09 |
DE102006030678A1 (en) | 2008-01-10 |
DE102006030678B4 (en) | 2009-05-14 |
ZA200705369B (en) | 2008-08-27 |
NO20073027L (en) | 2008-01-07 |
EP1876160B1 (en) | 2009-09-30 |
DE502007001607D1 (en) | 2009-11-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: INTERNATIONAL BUSINESS MACHINES CORPORATION, NEW Y Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:KOCH, ERNST-CHRISTIAN;REEL/FRAME:019497/0197 Effective date: 20070614 |
|
AS | Assignment |
Owner name: DIEHL BGT DEFENCE GMBH & CO., KG, GERMANY Free format text: CORRECTIVE ASSIGNMENT TO CORRECT THE THE RECEIVING PARTY DATA SHOULD READ;ASSIGNOR:KOCH, ERNST-CHRISTIAN;REEL/FRAME:019504/0337 Effective date: 20070614 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |