EP0509200B1 - Process for the fabrication of phlegmatized explosives - Google Patents
Process for the fabrication of phlegmatized explosives Download PDFInfo
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- EP0509200B1 EP0509200B1 EP92102032A EP92102032A EP0509200B1 EP 0509200 B1 EP0509200 B1 EP 0509200B1 EP 92102032 A EP92102032 A EP 92102032A EP 92102032 A EP92102032 A EP 92102032A EP 0509200 B1 EP0509200 B1 EP 0509200B1
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- European Patent Office
- Prior art keywords
- process according
- polymer
- roller
- explosive
- aqueous dispersion
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- 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.)
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- 239000002360 explosive Substances 0.000 title claims description 29
- 238000000034 method Methods 0.000 title claims description 17
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 229920000642 polymer Polymers 0.000 claims description 21
- 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 claims description 16
- 239000006185 dispersion Substances 0.000 claims description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 10
- 239000003380 propellant Substances 0.000 claims description 9
- 229940090898 Desensitizer Drugs 0.000 claims description 8
- 239000000028 HMX Substances 0.000 claims description 6
- UZGLIIJVICEWHF-UHFFFAOYSA-N octogen Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)CN([N+]([O-])=O)C1 UZGLIIJVICEWHF-UHFFFAOYSA-N 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 5
- 230000000996 additive effect Effects 0.000 claims description 5
- 239000002245 particle Substances 0.000 claims description 5
- 229920003023 plastic Polymers 0.000 claims description 5
- 239000004033 plastic Substances 0.000 claims description 5
- 239000002002 slurry Substances 0.000 claims description 4
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 claims description 3
- 239000008346 aqueous phase Substances 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- AYAQUZXJSZXBNY-UHFFFAOYSA-N ethenyl propanoate prop-2-enoic acid Chemical compound C(C=C)(=O)O.C(CC)(=O)OC=C AYAQUZXJSZXBNY-UHFFFAOYSA-N 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims 5
- 238000000576 coating method Methods 0.000 claims 5
- 230000035945 sensitivity Effects 0.000 description 14
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 3
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000000586 desensitisation Methods 0.000 description 2
- 238000005474 detonation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- -1 2-ethylhexyl Chemical group 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 241000169624 Casearia sylvestris Species 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003975 dentin desensitizing agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 230000009191 jumping Effects 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 239000002562 thickening agent 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
- C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
- C06B21/0033—Shaping the mixture
-
- 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
- C06B25/34—Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine
Definitions
- the invention relates to a method for producing phlegmatized, high-energy explosives, in particular hexogen (RDX) or octogen (HMX), as a component of plastic-bound explosives or propellant charge powder, in that the particulate explosive is coated with a desensitizing polymer from an aqueous phase.
- RDX hexogen
- HMX octogen
- Hexogen and octogen are characterized by a high energy or explosiveness for their use, which, however, causes considerable problems for processing.
- the high sensitivity to friction and impact leads to a correspondingly high security risk.
- This security risk is the higher, ever the grain size distribution is wider and the larger the coarse grain fraction is, since single grain detonations can then occur, for example, in propellant grains.
- Such single-grain detonations are also undesirable in use, especially when used in Lova-TLP.
- the coarse-grained fraction leads, for example, to intermittent burns in the case of TLP combustion interruptions, as a result of which the geometry of the propellant charge body changes in an uncontrolled manner and the combustion behavior and the ballistics are thus negatively influenced.
- any water moisture that may still be present is granulated in the same mixer.
- a wax is proposed as a desensitizer, which is dissolved in perchlorethylene.
- Graphite powder is also used added, which also has a desensitizing effect, in particular prevents electrostatic charges.
- a high-energy explosive produced in this way has a broad grain distribution with a high proportion of coarse grain, which not only shows the aforementioned disadvantages in processing, but is also responsible for certain technical defects.
- These explosives cannot be added to the otherwise very advantageous processing of propellant powders and explosive mixtures in extruders, in particular twin screw extruders, since the security risk is too great.
- the invention has for its object to propose a method of the type mentioned, which on the one hand does not require environmentally harmful solvents, and on the other hand leads to desensitized explosives with low sensitivity to friction.
- This object is achieved in that the particulate explosive with a particle size of up to 20 »m slurried with the polymer in aqueous dispersion, the sludges applied to a rotating, heated roller, the application dried at a temperature> 100 ° C without pressure and after Drying is scraped off the roller.
- the process according to the invention can be carried out continuously and does not require any special precautions for workplace protection or environmental protection, since work is carried out in the aqueous phase.
- a homogeneous dispersion can be achieved, which can be applied to the roller without any safety risk and which is dried without pressure by mere evaporation.
- the explosive particles are coated homogeneously with the polymer.
- the polymer used for desensitization preferably also forms the plastic binder for the finished explosive or propellant powder, the polymer being added in the amount or a part thereof required for the end product.
- polystyrene-1,3-butadiene-acrylonitrile, vinyl propionate acrylate the polymer preferably being used in a 50 to 55% strength aqueous dispersion.
- polyvinyl alcohol can also be used as the polymer, the aqueous dispersion additionally containing glycerol.
- a surface-active additive is preferably added to the aqueous dispersion.
- a surface-active additive for example, highly disperse, amorphous silicon dioxide can be used as the surface-active additive.
- the aforementioned additive prevents the formation of vapor bubbles, which in turn will cause the layer to crack open and possibly flake off. Furthermore, the flowability and the quality of the order is improved.
- Adequate desensitization is obtained when the explosive is slurried with 5 to 25% by weight of polymer in aqueous dispersion.
- the explosive is preferably used with a grain size of up to 10 .mu.m, and the grain size spectrum can also be in the range between 3 and 5 .mu.m.
- the slurry applied to the roller is preferably dried at a roller temperature between 110 ° C and 150 ° C, preferably ⁇ 140 ° C, which allows relatively short residence times to be achieved. These can be, for example, in the range of 60 s and a little more if a roller of at least 150 cm is used and the layer thickness is ⁇ 10 mm.
- An inventive desensitized RDX with a higher polymer content e.g. B. in the range of 15 to 25% can be used directly as basic granules when extruding LOVA propellant powder.
- a test series with hexogen (RDX) with a grain size of 10 »m and various polymers is shown in Table I in accordance with the annex, and the friction sensitivity and impact sensitivity determined in each case are listed.
- the desensitizers are shown in capital letters, which are explained in the footnote to the table.
- the example shows similarly good results in terms of sensitivity to friction with 75% by weight RDX and 25% by weight polymer A dispersed in water.
- the impact sensitivity in this case is 0.35 kgm.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Lubricants (AREA)
Description
Die Erfindung betrifft ein Verfahren zur Herstellung von phlegmatisiertem, hochenergetischem Sprengstoff, insbesondere Hexogen (RDX) oder Oktogen (HMX), als Bestandteil kunststoffgebundener Sprengstoffe oder Treibladungspulver, indem der partikelförmige Sprengstoff mit einem phlegmatisierenden Polymer aus wäßriger Phase überzogen wird.The invention relates to a method for producing phlegmatized, high-energy explosives, in particular hexogen (RDX) or octogen (HMX), as a component of plastic-bound explosives or propellant charge powder, in that the particulate explosive is coated with a desensitizing polymer from an aqueous phase.
Bei Treibladungspulvern, wie auch bei kunststoffgebundenen Sprengstoffen ist es bekannt, als wesentliche Komponente hochenergetische Sprengstoffe, wie Hexogen, Oktogen oder dergleichen, beizumischen. Hexogen und Oktogen zeichnen sich durch eine für ihren Einsatz bestimmende hohe Energie bzw. Brisanz aus, die jedoch für die Verarbeitung erhebliche Probleme mit sich bringt. Die hohe Reib- und Schlagempfindlichkeit führt zu einem entsprechend hohen Sicherheitsrisiko. Dieses Sicherheitsrisiko ist um so höher, je breiter die Kornverteilung und je größer der Grobkornanteil ist, da es dann beispielsweise in einem Treibladungspulver (propellant grains) zu Einzelkorn-Detonationen kommen kann. Solche Einzelkorn-Detonationen sind auch in der Anwendung, insbesondere bei Einsatz in Lova-TLP unerwünscht. Der Grobkornanteil führt beispielsweise bei TLP-Abbrandunterbrechungen zu Lochbrand, wodurch sich die Geometrie des Treibladungskörpers unkontrolliert verändert und somit das Abbrandverhalten und die Ballistik negativ beeinflußt werden.In propellant powders, as well as in plastic-bound explosives, it is known to add high-energy explosives, such as hexogen, octogen or the like, as an essential component. Hexogen and octogen are characterized by a high energy or explosiveness for their use, which, however, causes considerable problems for processing. The high sensitivity to friction and impact leads to a correspondingly high security risk. This security risk is the higher, ever the grain size distribution is wider and the larger the coarse grain fraction is, since single grain detonations can then occur, for example, in propellant grains. Such single-grain detonations are also undesirable in use, especially when used in Lova-TLP. The coarse-grained fraction leads, for example, to intermittent burns in the case of TLP combustion interruptions, as a result of which the geometry of the propellant charge body changes in an uncontrolled manner and the combustion behavior and the ballistics are thus negatively influenced.
Um das sicherheitstechnische Risiko bei der Verarbeitung und die anwendungstechnischen Nachteile zu reduzieren, ist es bekannt, diese hochenergetischen Sprengstoffe zu phlegmatisieren (DE-OS 37 11 995). Zu diesem Zweck wird der Sprengstoff angefeuchtet und beispielsweise in einem Zwangsmischer unter gleichzeitiger Erwärmung mit Wachs überzogen. Ferner ist es bekannt, den körnigen Sprengstoff in einem Kneter oder Mischer mit einem in flüssiger Phase vorliegenden Phlegmatisator zu überziehen. Zu diesem Zweck wird der eigentliche Phlegmatisator mit einem Lösungsmittel gelöst, gegenüber welchem der Sprengstoff nicht oder nur wenig löslich ist. Der körnige Sprengstoff wird in die Lösung nahe deren Siedetemperatur eingemischt.In order to reduce the safety-related risk during processing and the application-related disadvantages, it is known to desensitize these high-energy explosives (DE-OS 37 11 995). For this purpose, the explosive is moistened and, for example, coated with wax in a compulsory mixer with simultaneous heating. It is also known to coat the granular explosive in a kneader or mixer with a desensitizer present in the liquid phase. For this purpose, the actual desensitizer is dissolved with a solvent with which the explosive is insoluble or only slightly soluble. The granular explosive is mixed into the solution near its boiling point.
Nach dem Abzug des Lösungsmittels und der eventuell noch vorhandenen Wasserfeuchtigkeit wird im gleichen Mischer granuliert. Dies geschieht im Rahmen einer sogenannten Aufbaugranulierung, indem bei einer Kornverteilung zwischen 1 und 100 »m der Kornanteil bis 50 »m gesondert granuliert und agglomeriert sowie mit einer gemeinsamen Phlegmatisatschicht überzogen wird, während groberes Korn einzeln mit dem Phlegmatisator überzogen wird. Im Falle von Hexogen (RDX) wird als Phlegmatisator ein Wachs vorgeschlagen, das in Perchlorethylen gelöst wird. Ferner wird Graphitpulver zugegeben, das gleichfalls eine phlegmatisierende Wirkung hat, insbesondere elektrostatischen Aufladungen vorbeugt.After the solvent has been removed and any water moisture that may still be present is granulated in the same mixer. This takes place in the context of a so-called build-up granulation, in which, with a grain distribution between 1 and 100 »m, the grain fraction up to 50» m is separately granulated and agglomerated and coated with a common desensitizing layer, while coarse grain is coated individually with the desensitizing agent. In the case of hexogen (RDX), a wax is proposed as a desensitizer, which is dissolved in perchlorethylene. Graphite powder is also used added, which also has a desensitizing effect, in particular prevents electrostatic charges.
Ein solchermaßen hergestellter hochenergetischer Sprengstoff weist eine breite Kornverteilung mit einem hohen Anteil von Grobkorn auf, das nicht nur die vorgenannten Nachteile bei der Verarbeitung zeigt, sondern auch für gewisse anwendungstechnische Mängel verantwortlich ist. Diese Sprengstoffe lassen sich auch nicht bei der ansonsten sehr vorteilhaften Verarbeitung von Treibladungspulvern und Sprengstoffmischungen in Extrudern, insbesondere Doppelschnecken-Extrudern (twin screw extruder) zusetzen, da das Sicherheitsrisiko zu groß ist.A high-energy explosive produced in this way has a broad grain distribution with a high proportion of coarse grain, which not only shows the aforementioned disadvantages in processing, but is also responsible for certain technical defects. These explosives cannot be added to the otherwise very advantageous processing of propellant powders and explosive mixtures in extruders, in particular twin screw extruders, since the security risk is too great.
Schließlich ist es bekannt (DE-C-39 34 368), den Phlegmatisator unmittelbar in das Sprengstoffkorn einzubauen, indem der Sprengstoff gelöst und in gelöster Form mit dem Phlegmatisator in flüssiger Phase gemischt und die Mischung durch Sprühtrocknen in die feste Phase mit einer Korngröße bis zu 5 »m übergeführt wird. Als Phlegmatisator werden beispielsweise eingesetzt: Dibutylphthalat (DBP) oder Di-(2-ethylhexyl)-adipinat (DOA). Die Reibempfindlichkeit, die die maßgebliche physikalische Größe für die sichere Verarbeitung im Extruder ist, liegt bei Einsatz von DOA bei 30 kg, bei Einsatz von DBP bei 14,4 kg Stiftbelastung. Von Nachteil bei diesem Verfahren ist das Arbeiten mit Lösungsmittel, was entsprechende Vorkehrungen zur Einhaltung der zulässigen Arbeitsplatzkonzentrationen, wie auch zur Vermeidung von Umweltbelastungen erfordert.Finally, it is known (DE-C-39 34 368) to incorporate the desensitizer directly into the explosive grain by dissolving the explosive and mixing it in solution with the desensitizer in the liquid phase and spray-drying the mixture into the solid phase with a particle size up to is transferred to 5 »m. The following are used as desensitizers: dibutyl phthalate (DBP) or di (2-ethylhexyl) adipinate (DOA). The friction sensitivity, which is the decisive physical parameter for safe processing in the extruder, is 30 kg when using DOA and 14.4 kg when using DBP. Working with solvents is a disadvantage of this method, which requires appropriate precautions to maintain the permissible workplace concentrations and to avoid environmental pollution.
Der Erfindung liegt die Aufgabe zugrunde, ein Verfahren der eingangs genannten Art vorzuschlagen, das einerseits ohne umweltbelastende Lösungsmittel auskommt, andererseits zu phlegmatisierten Sprengstoffen geringer Reibempfindlichkeit führt.The invention has for its object to propose a method of the type mentioned, which on the one hand does not require environmentally harmful solvents, and on the other hand leads to desensitized explosives with low sensitivity to friction.
Diese Aufgabe wird erfindungsgemäß dadurch gelöst, daß der partikelförmige Sprengstoff mit einer Korngröße bis 20 »m mit dem Polymer in wäßriger Dispersion aufgeschlämmt, die Schlämme auf eine umlaufende, beheizte Walze aufgetragen, der Auftrag bei einer Temperatur > 100 °C drucklos getrocknet und nach dem Trocknen von der Walze abgeschabt wird.This object is achieved in that the particulate explosive with a particle size of up to 20 »m slurried with the polymer in aqueous dispersion, the sludges applied to a rotating, heated roller, the application dried at a temperature> 100 ° C without pressure and after Drying is scraped off the roller.
Das erfindungsgemäße Verfahren läßt sich kontinuierlich durchführen und bedarf keiner besonderen Vorkehrungen zum Arbeitsplatz- bzw. Umweltschutz, da in wäßriger Phase gearbeitet wird. Im Verein mit der geringen Korngröße läßt sich eine homogene Dispersion erzielen, die auf die Walze ohne sicherheitstechnisches Risiko aufgetragen werden kann und drucklos durch bloßes Abdampfen getrocknet wird. Nach dem Abschaben der getrockneten Schicht sind die Sprengstoffpartikel mit dem Polymer homogen beschichtet. Das der Phlegmatisierung dienende Polymer bildet vorzugsweise zugleich den Kunststoffbinder für den fertigen Sprengstoff bzw. das fertige Treibladungspulver, wobei das Polymer in der für das Endprodukt erforderlichen Menge oder einem Teil derselben zugegeben wird.The process according to the invention can be carried out continuously and does not require any special precautions for workplace protection or environmental protection, since work is carried out in the aqueous phase. In combination with the small grain size, a homogeneous dispersion can be achieved, which can be applied to the roller without any safety risk and which is dried without pressure by mere evaporation. After scraping off the dried layer, the explosive particles are coated homogeneously with the polymer. The polymer used for desensitization preferably also forms the plastic binder for the finished explosive or propellant powder, the polymer being added in the amount or a part thereof required for the end product.
Als besonders vorteilhaft hat sich erwiesen, das Polymer aus der Gruppe Styrol-1,3-Butadien-Acrylnitril, Vinylpropionat-Acrylat auszuwählen, wobei das Polymer vorzugsweise in einer 50 bis 55%igen wäßrigen Dispersion verwendet wird.It has proven to be particularly advantageous to select the polymer from the group styrene-1,3-butadiene-acrylonitrile, vinyl propionate acrylate, the polymer preferably being used in a 50 to 55% strength aqueous dispersion.
Statt dessen kann als Polymer auch Polyvinylalkohol verwendet werden, wobei die wäßrige Dispersion zusätzlich Glycerin enthält.Instead, polyvinyl alcohol can also be used as the polymer, the aqueous dispersion additionally containing glycerol.
Vorzugsweise wird der wäßrigen Dispersion ein oberflächenaktives Additiv zugegeben. Beispielsweise kann als oberflächenaktives Additiv hochdisperses, amorphes Siliciumdioxid verwendet werden.A surface-active additive is preferably added to the aqueous dispersion. For example, highly disperse, amorphous silicon dioxide can be used as the surface-active additive.
Das vorgenannte Additiv verhindert aufgrund seiner oberflächenaktiven Wirkung die Entstehung von Dampfblasen, die wiederum zum Aufspringen und gegebenenfalls Abplatzen der Schicht führen werden. Ferner wird die Fließfähigkeit und die Qualität des Auftrags verbessert.Due to its surface-active effect, the aforementioned additive prevents the formation of vapor bubbles, which in turn will cause the layer to crack open and possibly flake off. Furthermore, the flowability and the quality of the order is improved.
Eine ausreichende Phlegmatisierung wird dann erhalten, wenn der Sprengstoff mit 5 bis 25 Gew% Polymer in wäßriger Dispersion aufgeschlämmt wird.Adequate desensitization is obtained when the explosive is slurried with 5 to 25% by weight of polymer in aqueous dispersion.
Der Sprengstoff wird vorzugsweise mit einer Korngröße bis zu 10 um verwendet, wobei das Korngrößenspektrum durchaus auch im Bereich zwischen 3 und 5 »m liegen kann.The explosive is preferably used with a grain size of up to 10 .mu.m, and the grain size spectrum can also be in the range between 3 and 5 .mu.m.
Die auf die Walze aufgetragene Schlämme wird vorzugsweise bei einer Walzentemperatur zwischen 110 °C und 150 °C, vorzugsweise < 140 °C getrocknet, womit sich relativ kurze Verweilzeiten erreichen lassen. Diese können beispielsweise im Bereich von 60 s und wenig darüber liegen, wenn eine Walze von mindestens 150 cm verwendet wird und die Schichtdicke < 10 mm beträgt.The slurry applied to the roller is preferably dried at a roller temperature between 110 ° C and 150 ° C, preferably <140 ° C, which allows relatively short residence times to be achieved. These can be, for example, in the range of 60 s and a little more if a roller of at least 150 cm is used and the layer thickness is <10 mm.
Ein erfindungsgemäß phlegmatisiertes RDX mit höherem Polymer-Gehalt, z. B. im Bereich von 15 bis 25 % läßt sich unmittelbar als Grundgranulat beim Extrudieren von LOVA-Treibladungspulver verwenden.An inventive desensitized RDX with a higher polymer content, e.g. B. in the range of 15 to 25% can be used directly as basic granules when extruding LOVA propellant powder.
In der Tabelle I gemäß Anlage ist eine Versuchsreihe mit Hexogen (RDX) der Korngröße 10 »m und verschiedenen Polymeren wiedergegeben und die jeweils festgestellte Reibempfindlichkeit und Schlagempfindlichkeit aufgeführt. Hierbei sind die Phlegmatisatoren mit Großbuchstaben angegeben, die in der Fußnote zu der Tabelle erläutert sind.A test series with hexogen (RDX) with a grain size of 10 »m and various polymers is shown in Table I in accordance with the annex, and the friction sensitivity and impact sensitivity determined in each case are listed. The desensitizers are shown in capital letters, which are explained in the footnote to the table.
Die besten Ergebnisse bezüglich Reib- und Schlagempfindlichkeit zeigen die Versuchsbeispiele mit 75 Gew% RDX und einer Dispersion aus dem Polymer D mit 15 Gew%, Glycerin mit 10 Gew% und Wasser. Die Reibempfindlichkeit liegt bei über 36 kg Stiftbelastung, die Schlagempfindlichkeit bei 0,55 kgm.The best results with regard to friction and impact sensitivity are shown by the test examples with 75% by weight RDX and a dispersion from polymer D with 15% by weight, glycerin with 10% by weight and water. The friction sensitivity is over 36 kg pin load, the impact sensitivity at 0.55 kgm.
Ähnlich gute Ergebnisse hinsichtlich der Reibempfindlichkeit zeigt das Beispiel mit 75 Gew% RDX und 25 Gew% Polymer A in Wasser dispergiert. Die Schlagempfindlichkeit beträgt in diesem Fall 0,35 kgm.The example shows similarly good results in terms of sensitivity to friction with 75% by weight RDX and 25% by weight polymer A dispersed in water. The impact sensitivity in this case is 0.35 kgm.
Auch bei einem sehr hohen Hexogenanteil von 90 % wurde mit dem Polymer A mit 10 Gew%, dispergiert in Wasser, noch eine Reibempfindlichkeit von 32,4 kg Stiftbelastung und eine Schlagempfindlichkeit bei 0,30 kgm festgestellt.Even with a very high hexogen content of 90%, polymer A with 10% by weight, dispersed in water, still found a sensitivity to rubbing of 32.4 kg of pin load and a sensitivity to impact at 0.30 kgm.
In Tabelle II sind die gleichen Daten für ein Hexogen kleinerer Korngröße (5 »m) aufgezeichnet. Ferner ist in allen Versuchsreihen handelsübliches "Aerosil 200" (hochdisperses, amorphes Siliciumdioxid) zugegeben worden. Hierbei handelt es sich um ein Verdickungsmittel auf Kieselsäurebasis, das zu einer gleichmäßigen Verteilung des Auftrags auf der Walze führt und ein Abspringen der trocknenden Schicht auf der Walze verhindert.
Claims (13)
- Process for the production of desensitized, high-energy explosive, particularly hexogen (RDX) or octogen (HMX), as a component of plastic-bound explosives or propellants, in that a particulate explosive is coated with a desensitizing polymer from the aqueous phase, characterized in that the particulate explosive with a particle size up to 20 um is suspended with the polymer in aqueous dispersion, the slurry is applied to a rotating, heated roller, the coating is dried in pressureless manner at a temperature of >100°C and after drying is scraped from the roller.
- Process according to claim 1, characterized in that the polymer is chosen from the group styrene-1,3-butadiene-acrylonitrile, vinyl propionate-acrylate.
- Process according to claim 1 or 2, characterized in that the polymer is used in a 50 to 55% aqueous dispersion.
- Process according to claim 1, characterized in that polyvinyl alcohol is used as the polymer and the aqueous dispersion also contains glycerol.
- Process according to any one of the claims 1 to 4, characterized in that a surface-active additive is added to the aqueous dispersion.
- Process according to any one of the claims 1 to 5, characterized in that highly disperse, amorphous silicon dioxide is used as the surface-active additive.
- Process according to any one of the claims 1 to 6, characterized in that the desensitizer is constituted by a polymer serving simultaneously as a plastic binder for the explosive or the propellant.
- Process according to any one of the claims 1 to 7, characterized in that the explosive is suspended with 5 to 25% by weight polymer in aqueous dispersion.
- Process according to any one of the claims 1 to 8, characterized in that explosive with a particle size up to 10 »m is used.
- Process according to any one of the claims 1 to 9, characterized in that the coating on the roller is dried at a temperature between 110 and 150°C.
- Process according to any one of the claims 1 to 10, characterized in that the coating on the roller is dried at a temperature between 110 and 140°C.
- Process according to any one of the claims 1 to 11, characterized in that the slurry is applied to a roller having a circumference of at least 150 cm and the residence time of the coating on the roller is > 60 s.
- Process according to any one of the claims 1 to 12, characterized in that the slurry is applied to the roller in a coating thickness of < 10 mm.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4111752A DE4111752C1 (en) | 1991-04-11 | 1991-04-11 | |
DE4111752 | 1991-04-11 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0509200A1 EP0509200A1 (en) | 1992-10-21 |
EP0509200B1 true EP0509200B1 (en) | 1995-07-05 |
Family
ID=6429315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP92102032A Expired - Lifetime EP0509200B1 (en) | 1991-04-11 | 1992-02-07 | Process for the fabrication of phlegmatized explosives |
Country Status (3)
Country | Link |
---|---|
US (1) | US5547527A (en) |
EP (1) | EP0509200B1 (en) |
DE (2) | DE4111752C1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6893516B2 (en) | 2001-11-14 | 2005-05-17 | Diehl Munitionssysteme Gmbh & Co. Kg | Insensitive pressable explosive |
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DE4324739C1 (en) * | 1993-07-23 | 1994-09-08 | Deutsche Aerospace | Cast polymer-bonded explosive charge |
FR2728562B1 (en) * | 1994-12-22 | 1997-01-24 | Poudres & Explosifs Ste Nale | METHOD FOR THE CONTINUOUS MANUFACTURING OF PYROTECHNICAL CHARGERS WITH A SILICONE BINDER AND COMPOSITIONS LIKELY TO BE IMPLEMENTED BY THIS METHOD |
DE19605346C1 (en) * | 1996-02-14 | 1997-07-24 | Fraunhofer Ges Forschung | Phlegmatised energy carrier |
CA2253500A1 (en) * | 1996-05-03 | 1997-11-13 | Ralph Edward Dawson | Explosive formulations |
WO1997042140A1 (en) * | 1996-05-03 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
IL126664A0 (en) * | 1996-05-03 | 1999-08-17 | Eastman Chem Co | Explosive formulations |
US5808234A (en) * | 1996-05-06 | 1998-09-15 | Eastman Chemical Company | Explosive formulations |
AU3129097A (en) * | 1996-10-15 | 1998-05-11 | Eastman Chemical Company | Explosive formulations |
DE19907809C2 (en) * | 1999-02-24 | 2002-10-10 | Nitrochemie Gmbh | Process for the production of one-, two- or three-base propellant charge powders for gun ammunition |
ZA200205775B (en) * | 2002-04-12 | 2003-03-28 | Diehl Munitionssysteme Gmbh | Insensitive hexogen explosive. |
FR2925488B1 (en) * | 2007-12-19 | 2011-12-23 | Snpe Materiaux Energetiques | CRYSTAL COATING DENSIBILIZATION OF EXPLOSIVE ENERGY SUBSTANCES; CRYSTALS SUCH AS COATED SUBSTANCES, ENERGY MATERIALS. |
US8575074B2 (en) | 2011-06-06 | 2013-11-05 | Los Alamos National Security, Llc | Insensitive explosive composition and method of fracturing rock using an extrudable form of the composition |
CN103012299B (en) * | 2012-12-27 | 2015-01-14 | 中国工程物理研究院化工材料研究所 | HMX preparation method based on DMSO/H20 (Dimethyl Sulfoxide/H2O) binary system |
US9850180B1 (en) * | 2015-02-12 | 2017-12-26 | The United States Of America As Represented By The Secretary Of The Army | Method for manufacture of amorphous energetics |
RU2734192C1 (en) * | 2020-03-12 | 2020-10-13 | Акционерное общество "Взрывгеосервис" | Explosive composition for making charges of cumulative perforators (embodiments) |
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US1036906A (en) * | 1912-08-27 | O Reuter | Granular explosive, especially suitable for the preparation of pressed pieces, and method of making the same. | |
US1007276A (en) * | 1909-09-24 | 1911-10-31 | Du Pont Powder Co | Method of solidifying crystallizable mixtures without substantial crystallization. |
US2438281A (en) * | 1945-12-10 | 1948-03-23 | Us Sec War | Method for processing plastic sheets |
US3348986A (en) * | 1955-02-04 | 1967-10-24 | Charles W Sauer | Process of preparing plastic coated high explosive particles and articles |
US3296041A (en) * | 1964-07-08 | 1967-01-03 | Eastman Kodak Co | Granulated crystalline plastic bonded explosives |
US3266957A (en) * | 1964-09-24 | 1966-08-16 | Richard H Stresau | Booster explosive of ultrafine desensitized cyclotrimethylene-trinitramine and method of preparing same |
US3338764A (en) * | 1965-08-19 | 1967-08-29 | Du Pont | Flexible detonating compositions containing high explosives and polymeric metallocarboxylates |
US3428502A (en) * | 1966-10-25 | 1969-02-18 | Du Pont | Polyvinyl acetate binder for crystalline explosive |
US3586551A (en) * | 1968-08-27 | 1971-06-22 | Du Pont | Water-degradable cap-sensitive selfsupporting explosive |
US4163681A (en) * | 1970-04-15 | 1979-08-07 | The United States Of America As Represented By The Secretary Of The Navy | Desensitized explosives and castable thermally stable high energy explosive compositions therefrom |
FR2135534B1 (en) * | 1971-05-06 | 1973-06-29 | Wasagchemie Ag | |
US4113811A (en) * | 1975-07-02 | 1978-09-12 | Dynamit Nobel Aktiengesellschaft | Process for the production of flexible explosive formed charges |
US4092187A (en) * | 1976-08-18 | 1978-05-30 | The United States Of America As Represented By The Secretary Of The Army | Process for coating crystalline high explosives |
NO144666C (en) * | 1980-02-29 | 1981-10-14 | Dyno Industrier As | PROCEDURE FOR PREPARING ALUMINUM-CONTAINING HIGH-ENERGY EXPLOSIVE MIXTURES |
DE3010052C2 (en) * | 1980-03-15 | 1982-09-09 | Friedrich-Ulf 8899 Rettenbach Deisenroth | Process for the production of plastic-bound explosives |
CA1195122A (en) * | 1981-05-25 | 1985-10-15 | Paul Arni | Process for preparing a high power explosive, high power explosive produced thereby and method for shaping a high power |
DE3234978C1 (en) * | 1982-09-22 | 1984-01-26 | Messerschmitt-Bölkow-Blohm GmbH, 8000 München | Cast explosive charge |
NO153804C (en) * | 1984-02-08 | 1986-05-28 | Dyno Indusrtrier A S Nitroglyc | PROCEDURE FOR THE COATING OF CRYSTALLINE HEAD EXPLOSIVES. |
DE3625412A1 (en) * | 1986-07-26 | 1988-02-04 | Messerschmitt Boelkow Blohm | METHOD FOR PRODUCING A PLASTIC-TIED EXPLOSIVE |
DE3711995A1 (en) * | 1987-04-09 | 1988-10-20 | Messerschmitt Boelkow Blohm | Desensitising explosives or propellants - comprises mixing them with desensitiser e.g. graphite dissolved in a liq. solvent, evaporating solvent etc. |
JPH07112537B2 (en) * | 1987-11-27 | 1995-12-06 | ダイセル化学工業株式会社 | Method for mixing raw material composition of highly ignitable or explosive substance |
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DE3804396C1 (en) * | 1988-02-12 | 1989-05-18 | Messerschmitt-Boelkow-Blohm Gmbh, 8012 Ottobrunn, De | Process for producing plastic-bonded explosives |
DE3934368C1 (en) * | 1989-10-14 | 1990-11-15 | Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung Ev, 8000 Muenchen, De |
-
1991
- 1991-04-11 DE DE4111752A patent/DE4111752C1/de not_active Expired - Fee Related
-
1992
- 1992-02-07 EP EP92102032A patent/EP0509200B1/en not_active Expired - Lifetime
- 1992-02-07 DE DE59202779T patent/DE59202779D1/en not_active Expired - Fee Related
-
1993
- 1993-08-16 US US08/106,789 patent/US5547527A/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
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CHEMICAL ABSTRACTS, vol. 070, no. 24, 16. Juni 1969, Columbus, Ohio, US;abstract no. 107929G, 'Solid self-supporting explosives' Seite 104; and CS-A-127 990 (J. Vacek et al.) 15.06 1968 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6893516B2 (en) | 2001-11-14 | 2005-05-17 | Diehl Munitionssysteme Gmbh & Co. Kg | Insensitive pressable explosive |
Also Published As
Publication number | Publication date |
---|---|
EP0509200A1 (en) | 1992-10-21 |
DE4111752C1 (en) | 1992-09-17 |
US5547527A (en) | 1996-08-20 |
DE59202779D1 (en) | 1995-08-10 |
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