巴西专利BR112012025036B1 non-toxic heavy metal-free explosive sensitivity initiators and methods of preparing the same

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专利摘要:
sensitized explosive percussion primers free of heavy metal, non-toxic and methods of preparing them. a non-toxic, non-hygroscopic percussion primer composition and methods of preparing them, including at least one explosive component that has traditionally been regarded as a moderately insensitive explosive or secondary explosive and at least one component of the fuel particles that it has a particle size of about 1.5 microns and about 12 microns, which allows the use of moderately active metal oxidizers. The sensitivity of the primer composition is created by the interaction between the moderately insensitive explosive and the fuel agent in such a way that traditional primary explosives, such as lead styphnate or ddnp are not required. the booklet composition also eliminates the risks and dangers associated with traditional nano-sized fuel particles.
公开号:BR112012025036B1
申请号:R112012025036
申请日:2011-03-29
公开日:2020-04-07
发明作者:A Quinn Aaron；Erickson Jack；Sandstrom Joel
申请人:Alliant Techsystems Inc；Vista Outdoor Operations Llc；
IPC主号:

专利说明:

FREE EXPLOSIVE SENSITIVITY PERCUSSION INITIATORS FREE OF HEAVY, NON-TOXIC METAL AND METHODS OF PREPARATION OF THE SAME
FIELD OF THE INVENTION
The present invention relates to the compositions of the initiators for non-hydroscopic, non-toxic, heavy metal-free explosive systems, and methods for making them.
BACKGROUND OF THE INVENTION
Mixtures of conventional percussion starters of almost all small arms ammunition gauges of traditionally used, mostly, a combination of lead stifinate as the explosive starter, with antimony sulfide as the fuel and barium nitrate as the oxidant in various proportions. In addition to these compounds containing lead, antimony and barium, several other compounds containing objectionable chemicals such as mercury, potassium chlorate and the like have also been used in percussion initiators in various proportions. Due to toxicity, ecological impact, corrosivity, and / or expensive handling procedures during the production and disposal of such objectionable chemicals, an effort has been made to replace compounds containing such objectionable chemicals in ammunition initiators.
The Department of Defense (DOD) and the Department of Energy (DOE) have made a significant effort to find substitutes for percussion initiators based on toxic metals. In addition, firing ranges and other firearms sites have severely limited the use of ammunition
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2/36 toxic metal compounds due to the potential health and handling risks associated with the use of lead, barium and antimony.
Ignition devices have traditionally been based on the sensitivity of a primary explosive, which significantly limits available primary explosives. The most common alternative to lead stifinate is diazodinitrophenol (DDNP). DDNP-based primers, however, because they do not fully meet the requirements of commercial or military reliability and have, for several decades, been used only in training ammunition, as such primers suffer from poor reliability that can be attributed to the low friction sensitivity. , the low temperature of the flame and the fact that they are hygroscopic. The ability of a percussion initiator to function reliably at low temperatures becomes particularly important when ammunition percussion preparations are used in severe cold, such as in aircraft weapon systems that are routinely exposed to severe cold.
Another potential substitute for lead stifinate that has been identified is metastable interstitial (MIC) composites (also known as metastable nanoenergetic composites (MNC), nanothermites or superthermites), which includes Al-MoO3, Al-WO3, AL-CuO and AlBi2203 . In these composites, both the aluminum powder and the oxidizing material have a particle size less than 0.1 micron and more preferable between 20 to 50 nanometers. The termite interaction between the fuel and the oxidant resulting from the high surface area and the minimum layer of
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3/36 oxide in the fuel resulted in excellent performance characteristics, such as impact sensitivity, high temperature output and reliability under established conditions (-18.33 ° C to 71.11 ° C). However, it has been found that these systems, despite their excellent performance characteristics, are difficult to process safely and economically on a large scale. The main difficulty is the handling of nanometric powder mixtures due to their sensitivity to friction and electrostatic discharge (ESD) and their reactivity in the air. See Pat. No. 5,717,159 and U.S. Patent Publication No. 2006/0113014. As a result, much technology has been devoted to the safe and economical handling of these nanometric materials.
Yet another potential substitute for lead stifinate that has been identified is compounds that contain moderately insensitive explosives that are sensitized by nanometer fuel particles. The explosive in such compounds is moderately insensitive to shock, friction and heat according to industry standards and has generally been categorized as a secondary explosive due to its relative insensitivity. Examples of such energizers include CL-20, PETN, RDX, HMX, nitrocellulose and mixtures thereof. The nanometric fuel particles have an average size of less than 1500 nanometers and more appropriately less than 650 nanometers, which can include aluminum, boron, molybdenum, silicon, titanium, tungsten, magnesium, melamine, zirconium, calcium silicate or mixtures thereof. See, for example, U.S. Patent Publication No. 2006/0219341 and U.S. Patent Publication No. 2008/0245252.
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However, safety and economic efficiency continue to be of concern due to the nanometric fuel particles, although such compounds exhibit excellent performance characteristics.
In light of the problems identified above, there is still a need for the technique for a percussion initiator that is free of toxic metals, is non-corrosive and non-erosive, can be processed and handled safely and economically, has sensitivity and ignition characteristics. superior performance compared to traditional initiator mixtures, contain non-hydroscopic properties, are stable over a wide range of temperatures and storage conditions and are cheaper to produce than conventional heavy metal initiator mixtures.
BRIEF SUMMARY OF THE INVENTION
In one aspect, the present invention relates to a composition of the initiator, including at least one moderately sensitive explosives that is a member selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN), CL-20, RDX, HMX, TNT, nitroguanidine, stifinic acid, potassium benzofuroxan dinitro (KDNBF) and mixtures thereof and at least one fuel particle, having an average particle size of about 1.5 microns to about 12 microns.
In another aspect, the present invention relates to a primer composition in which at least one moderately insensitive explosive and a micrometric fuel particle provide an explosive fuel system in which traditional primary explosives, such as
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5/36 lead stifinate and diazodinitrophenol (DDNP), are absent from the composition of the initiator.
In another aspect, the present invention relates to a composition of the initiator, including a moderately insensitive secondary explosive; at least one particle of fuel having an average particle size of about 1.5 microns to about 12 microns and a moderately active oxidizing metal selected from the group consisting of bismuth trioxide, bismuth subnitrate, bismuth tetroxide, sulfide of bismuth, zinc peroxide, tin oxide, manganese dioxide, molybdenum trioxide and their combinations.
In another aspect, the present invention relates to a suspension of particulate components in an aqueous medium, the particulate components, including three different particulate components, the particulate components which are moderately insensitive explosive particles which is a member selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN), CL20, RDX, HMX, TNT, nitroguanidine, stifinic acid, potassium dinitrobenzofuroxane (KDNBF) and mixtures thereof, a particle of fuel, having an average size between about 1.5 microns and 12 microns and oxidizer particles.
In another aspect, the present invention relates to a primer composition substantially devoid of a traditional primary explosive, but instead containing an explosive composite comprising a moderately insensitive explosive which is a member selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN), CL-20, RDX, HMX, TNT,
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6/36 nitroguanidine, stifinic acid, potassium dinitrobenzofuroxane (KDNBF) and mixtures thereof and at least one fuel particle component having a size between about 1.5 microns and 12 microns, in which the amount of explosive is moderately insensitive and hair at least one fuel particle component is on the starter premix is at least 11% by weight based on the dry weight of the ammo starter composition.
In another aspect, the present invention relates to an ammunition initiator, including at least one fuel particle component substantially devoid of all particles with a particle size of about 1000 nanometers or less.
In another aspect, the present invention relates to an artillery containing initiator including a housing, including at least one percussion initiator according to any of the above embodiments.
In another aspect, the present invention relates to a method for making a percussion initiator or igniter, the method, including providing at least one explosive moistened with water selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN) , CL-20, RDX, HMX, TNT, nitroguanidine, stifinic acid, potassium dinitrobenzofuroxane (KDNBF) and mixtures thereof, combining at least one fuel particle, having an average particle size between approximately 1.5 microns and about 12 microns with at least one explosive moistened with water to form a first mixture and the combination of at least one oxidizer with the first mixture.
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In another aspect, the present invention relates to a method for making a percussion initiator, the method, including at least one explosive moistened with water selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN), CL-20, RDX, HMX, TNT, nitroguanidine, stifinic acid, potassium dinitrobenzofuroxane (KDNBF) and mixtures thereof, combining a plurality of fuel particles, having a particle size range of approximately 1.5 microns to about 12 microns with at least one explosive moistened with water to form a first mixture and combining at least one oxidizer with the first mixture.
In another aspect, the present invention relates to a method for making a percussion initiator, including at least one moistened explosive selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN), CL-20, RDX, HMX, TNT, nitroguanidine , stifinic acid, potassium dinitrobenzofuroxane (KDNBF) and mixtures thereof, combining at least one particle of fuel, having an average particle size of about 1.5 microns to about 12 microns at least one explosive moistened with water to form a first mixture and combining at least one oxidant, having an average particle size of about 1 micron to about 200 microns with the first mixture.
In another aspect, the present invention relates to a method for making a primer composition, including providing at least one explosive moistened with water selected from the group consisting of nitrocellulose, pentaerythritol tetranitrate (PETN), CL-20, RDX, HMX,
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TNT, nitroguanidine, stifinic acid, potassium dinitrobenzofuroxane (KDNBF) and their mixtures, combining a plurality of fuel particles, having an average particle size of 1.5 microns to about 12 microns with at least one explosive moistened with water and combining an oxidant with an average particle size of 1 micron to about 200 microns with the first mixture.
In any of the above modalities, the oxidizer can be combined with the explosive, with the first mixture or with the fuel particle component.
These and other aspects of the invention are described in the following detailed description of the invention or in the claim.
BRIEF DESCRIPTION OF THE DRAWINGS
The invention can be understood, more fully, taking into account the following detailed description of various modalities of the invention in connection with the accompanying drawings, in which:
Fig. 1A is a longitudinal section of a rimfire gun cartridge employing a percussion initiator composition of an embodiment of the invention.
FIG. 1B is an enlarged view of the anterior portion of the rimfire weapon cartridge shown in Fig. 1A.
Fig. 2A is a longitudinal section of a centerfire gun cartridge employing a centerfire percussion initiator of an embodiment of the invention.
Fig. 2B is an enlarged view of the center.2 ammunition starter in Fig.2A.
Fig. 3 is a schematic illustration of exemplary artillery in which a rocket launcher is used.
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9/36 an embodiment of the invention is used.
While the invention is subject to various modifications and alternative forms, details have been shown by way of example in the drawings and will be described in detail. It should be understood, however, that the intention is not to limit the invention to the particular embodiment described. On the contrary, the intention is to cover all modifications, equivalents and alternatives following the spirit and scope of the invention as defined by the added claims.
DETAILED DESCRIPTION OF THE INVENTION
While this invention can be incorporated in many different forms, they are described in detail here in a specific preferred embodiment of the invention. This description is an example of the principles of the invention and is not intended to limit the invention to the particular embodiment illustrated.
In one aspect, instead of containing a traditional primary explosive, the initiator compositions of the present invention contain an explosive composite comprising at least one moderately insensitive explosive and at least one fuel agent having a particle size between about 1.5 microns and 12 microns. The explosive in such compounds is moderately insensitive to shock, friction and heat according to industry standards and has generally been categorized as a secondary explosive due to its relative insensitivity. Examples of such CL-20, PETN, RDX, HMX, KDNBF, nitrocellulose and mixtures thereof. Examples of fuel agents for use with the energizer to form explosive composites include,
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10/36 but are not limited to, aluminum, boron, molybdenum, titanium, tungsten, magnesium, melamine, zirconium, calcium silicate and mixtures thereof.
The sensitivity of the explosive composite is created by the interaction between the moderately insensitive explosive and the fuel agent. The initiator compositions of the present invention are capable of performing the same function and meeting or exceeding the performance characteristics of common initiator compositions containing traditional heavy metal resulting in primary explosives, such as lead stipinate or other traditional primary explosives such as DDNP. This new explosive system also addresses the oxidant replacement problem experienced in starter formulations devoid of metallic oxidants (such as barium nitrate) creating enough heat to use less active, non-toxic oxidants. Not only can the traditional primary explosives and oxidants that are objectionable be eliminated from the compositions of the initiator of the present invention, but nanometric fuel components are substantially absent from compositions of the initiator of the present invention, which also eliminates the safety and cost-disadvantages. efficiency, similar to that. As a result, the compositions of the initiator of the present invention are completely non-toxic, non-hydroscopic, more economical and much safer to produce.
In one aspect, the present invention relates to compositions of the percussion initiator comprising at least one explosive compound, which contains at least one moderately insensitive explosive component and at least
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11/36 a fuel agent having a particle size of about 1.5 microns to about 12 microns, suitably about 2 microns to about 9 microns and more suitably about 3 microns to about 6 microns and at least one oxidizing agent.
In some embodiments, other components can be added to the initiator compositions, comprising at least one explosive composite and at least one oxidizer, such as a sensitizer to increase the sensitivity of the explosive component, a binder, floor propellants, additional fuel agents and / or additional explosive components.
Examples of appropriate classes of explosives include, but are not limited to, nitrate esters, nitramines, nitroaromatics and mixtures thereof. Explosives can be categorized into primary explosives and secondary explosives, depending on their relative sensitivity and common use within the industry, with secondary explosives being less sensitive than primary explosives. Secondary explosives can also be referred to as moderately insensitive explosives. Appropriately, the explosive employed in compositions of the percussion initiator of the present invention includes at least one moderately insensitive explosive that is typically referred to as a secondary explosive within the industry.
Examples of ester nitrate include, but are not limited to, PETN (pentaerythritol tetranitrate) and nitrocellulose. Nitrocellulose includes nitrocellulose ball powder and nitrocellulose fiber, having a high percentage of nitrogen, for example, between about 10%
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12/36 by weight and 13.6% by weight nitrogen.
Examples of nitramines include, but are not limited to CL-20, RDX, HMX and nitroguanidine. CL-20 is
2.4.6.8.10.12- hexanitrohexaazaisowurtzitano (HNIW) or
2.4.6.8.10.12- hexanitro-2,4,6,8,10,12-hexaazatetracyclo [5.5.0.0.5.903, ¹¹ ] -dodecane.
RDX (real demolition explosive), hexahydro-1,3,5,5-trinitro-1,3,5-triazine or 1,3,5-trinitro-1,3,5triazacyclohexane can also be referred to as cyclonite, hexagen or cyclotrimethylenetrinitramine. HMX (high melting explosive), octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine or 1,3,5,7-tetranitro-1,3,5,7 tetraazacyclooctane (HMX), it can also be referred to as cyclotetramethylene-tetranitramine or octagen, among other names.
Examples of nitroaromatics include, but are not limited to, tetryl (2.4.6-trinitrophenyl-methylnitramine), TNT (trinitrotoluene-2.4.6), TNR (2, 4, 6trinitroresorcinol or stifinic acid) and DDNP (diazodinitrophenol or dinol or 4 , 6-dinitrobenzene-2-diazol-oxide).
Examples of primary explosives include, but are not limited to, lead stifinate, metal azides, mercury fulminate and DDNP. As mentioned above, such primary explosives are undesirable for use as the primary explosive in the percussion initiator compositions of the present invention. In some embodiments, there is a substantially non-traditional primary explosive component present in the percussion initiator compositions of the present invention.
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Explosive used in the explosive composite of percussion initiator compositions includes explosives traditionally identified as a secondary explosive. Preferred moderately insensitive explosives according to the present invention include, but are not limited to, nitrocellulose, pentaerythritol tetranitrate (PETN), CL-20, RDX, HMX, TNT, nitroguanidine, stifinic acid, alkali metals and / or alkaline earths metallic salts of dinitrobenzofuroxanes such as potassium dinitrobenzofuroxane (KDNBF) and mixtures thereof. The amounts of moderately insensitive explosives in explosive composite of the initiator compositions according to the present invention can be between about 5 and 40% by weight, for example, based on the total composition of the initiator composition, more appropriately, between 8 and 20% in weight. The amount of moderately insensitive explosives can vary depending on the moderately insensitive explosive or combination of moderately insensitive explosives employed.
In some embodiments, nitrocellulose is used as a moderately insensitive explosive in the explosive composite. Nitrocellulose, particularly fibers having a high percentage of nitrogen, for example, greater than about 10% by weight nitrogen and having a high surface area, has been found to increase sensitivity. In starter compositions where the composition includes nitrocellulose fibers in the explosive composite, the temperatures of the flame created exceeded those of lead stifinate. In some embodiments, nitrocellulose fibers have a nitrogen content of approximately 12.5% in
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14/36 weight at about 13.6% by weight.
Moderately insensitive explosives can be of varying particle size. For example, particle size can reach about 0.1 micron to about 100 microns. The combination or mixture of more than one size and type can be effectively used to adjust the composition sensitivity of the initiator.
Examples of the fuel particles suitable for use with the energizer to form the composite here include, but are not limited to, aluminum, boron, molybdenum, titanium, tungsten, magnesium, melamine, zirconium, calcium silicate and mixtures thereof.
The fuel particle can have an average particle size between about 1.5 microns and 12 microns, more appropriately between about 2 microns and 9 microns and more appropriately between about 3 microns and 6 microns. In some embodiments, a plurality having a particle size distribution is employed. The fuel particle distribution can be between about 1.5 microns and 12 microns, more appropriately between about 2 microns and 9 microns and more appropriately between about 3 microns and 6 microns. The distribution can be unimodal or multimodal. Appropriately, the fuel particle generally has a spherical shape, although other shapes such as platelets can be used.
It is assumed that the sensitivity of the resulting explosive composite from the moderately insensitive explosive and the micro-sized fuel particle is a product of the resulting surface area between these components. Therefore, it has been observed that the quantities of one or more
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15/36 more explosive composite fuel particle components of the initiator compositions according to the present invention may be dependent on this surface area ratio so that less quantity is required for smaller particle sizes. For example, the amount of the fuel particle component may be less than 2 microns in particle size than 6 microns in particle size, while larger particle sizes have less contact surface area with the moderately insensitive explosive component. . Suitably, in particular embodiment, the dimensions of fuel micro particles are used in the composition of the initiator, on a dry weight basis, in an amount comprised between about 5 and 25% by weight, for example, based on the total composition of the initiator. , more suitably between about 6 and 12% by weight and more suitably between about 9 and 10% by weight.
It is desirable to have fur any less fence in 5% by weight, more appropriately, fur any less fence in 7% by weight and more appropriately fur any less fence in 9% by weight of
micron-sized fuel particles, based on the dry weight of the initiator composition.
In a particular embodiment, the fuel particles have an average fuel particle size of about 3 microns and are present in the amount of about 9% by weight. As a specific example, spherical aluminum fuel particles having an average particle size of about 3 microns in the amount of 9% by weight can be selected as the fuel agent in the explosive composite of the
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16/36 compositions of the initiator of the present invention.
As mentioned above, nano-sized fuel particles (1500 nm in size or less) are undesirable for use in the percussion initiator compositions of the present invention. In some embodiments, it is substantially free of nano-sized fuel particles in the percussion initiator compositions of the present invention.
A specific example of a fuel particle that can be employed here is Valimet ^TM spherical aluminum powder of micron size having an average particle size of about 2 microns to about 12 microns.
An oxidizer is suitably employed in the compositions of the initiator according to one or more embodiments of the invention. Oxidizers can be used in the initiator composition, on a dry weight basis, in an amount between about 35% by weight to about 80% by weight of the initiator composition, more appropriately, between about 50% by weight at about 70% by weight and more suitably between about 60% by weight and 67% by weight of the dry composition of the initiator. Appropriately, oxidizers employed here are moderately active metal oxides, non-hygroscopic and are not considered to be toxic so that they make the initiator composition moderately dense and reliable when combined with the explosive composite. Examples of such oxidants include, but are not limited to, bismuth trioxide, bismuth subnitrate, bismuth tetroxide, bismuth sulfide, zinc peroxide, tin oxide, manganese dioxide, molybdenum trioxide, potassium nitrate and combinations thereof .
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The oxidizer is not limited to any particular particle size. However, it may be more desirable for the oxidant to have an average particle size of about 1 micron to about 200 microns, more appropriately, about 10 microns to about 200 microns and more appropriately about 100 microns to about 200 microns. microns. In a particular embodiment, the oxidant employed is bismuth trioxide, having an average particle size of about 100 to about 200 microns, for example, about 177 microns, can be employed.
A sensitizer can be added to the percussion initiator compositions according to one or more embodiments of the invention. As the particle size of micron-sized fuel particles increases, sensitivity decreases. Thus, like its use in traditional lead stifinate formulations, the sensitizer can be beneficial in improving ignition uniformity. However, the sensitizer is not necessary to sensitize the compositions of the initiator of the present invention. Sensitizers can be employed in amounts of 0% by weight to about 10% by weight, suitably 0% by weight to about 8% by weight and more appropriately 0% by weight to about 4% by weight of the initiator composition . An example of an appropriate sensitizer includes, but is not limited to, tetracene.
The sensitizer can be used in combination with a friction agent. A chafing agent can also be employed in the compositions of the initiator of the present invention in the absence of a sensitizer. A chafing agent can also have sensitizing characteristics. Agents
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Friction 18/36 can be used in rimfire applications in amounts of about 0% by weight to about 25% by weight of the initiator composition. Examples of a suitable friction agent include, but are not limited to, glass powder, glass beads, calcium silicate, boron and mixtures thereof.
One or more propellant component can be added to the percussion initiator compositions in amounts from 0% by weight to about 20% by weight, suitably 0% by weight to about 10% by weight and more appropriately 0% by weight. weight at about 6% by weight of the initiator composition. Examples of a suitable propellant component include, but are not limited to, single or double base soil, such as Hercules.
Other conventional initiator additives as binders can be employed in the initiator compositions here as is known in the art. Synthetic and natural binders find use here. Examples of suitable binders include, but are not limited to, natural and synthetic gums, including xanthan, arabica, tragacanth, guar, karaya and polymeric synthetic binders such as hydroxypropyl cellulose and polypropylene oxide, as well as mixtures thereof. Binders can be added in amounts from about 0% by weight to about 5% by weight of the composition, suitably about 0% by weight to about 1.5% by weight of the composition and more appropriately about 0% by weight to about 1% by weight.
Other optional ingredients as are known in the art can also be used in the compositions according to one or more embodiments of the invention. For example, inert fillers, thinners, other binders,
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19/36 low-power explosives, etc., can be optionally added.
Buffers can optionally be added to the initiator compositions to decrease the likelihood of hydrolysis of the fuel particles and as a stabilizer, which is dependent on temperature and pH. See U.S. Patent Publication No. 2008/0245252 A1, all content which is incorporated by reference here. Such buffers can also include stifinic acid.
The above lists and scales are for illustrative purposes only and are not intended to limit the scope of the present invention.
In a preferred embodiment, the explosive composite of the initiator compositions of the present invention comprises a moderately insensitive explosive, such as nitrocellulose fiber, used in combination with an aluminum fuel particle with an average particle size between about 1.5 microns and 12 microns, more appropriately between about 2 microns and 9 microns and more appropriately between about 3 microns and 6 microns. A preferred oxidant is bismuth trioxide with an average particle size between about 1 micron and 200 microns, for example, about 100 microns to about 200 microns is employed.
The compositions of the initiator according to one or more embodiments of the invention can be processed with simple water processing techniques. The present invention allows the use of moderately insensitive explosive components which are moistened with water while the micron and component size fuel particles
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20/36 oxidizing agents are added as dry components, which are safer to handle, maintaining the sensitivity of the assembled primer. It is assumed that this can be attributed to the use of larger fuel particles. The milling and screening steps, which can be used for MIC-MNC formulations, are also eliminated. For at least these reasons, the processing of the initiator compositions according to the invention is safer and more cost efficient.
The method of making the initiator compositions according to one or more embodiments of the invention generally includes mixing a moderately insensitive explosive moistened with at least one fuel particle component having a particle size between about 1.5 and 12 microns to form a first mix. A dry oxidizer can be added to the first mixture, with the explosive moistened beforehand with at least one component of fuel particles, or with the explosive moistened in combination with, or simultaneously with at least one component of fuel particles. When the oxidizer is added in combination with at least one component of fuel particles, the oxidizer and at least one component of fuel particles can be mixed dry. The oxidizer can optionally be mixed dry with at least one other component, such as the binder, sensitizer, and / or propellant to form a second dry mixture and the second mixture, then added to the first mixture and mixing until homogenized to form a final mixture .
The method of making the initiator's compositions in
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21/36 according to one or more embodiments of the invention generally includes precipitating the moderately insensitive explosive over at least one fuel particle component having a particle size between about 1.5 and 12 microns to form a first homogeneous mixture. After homogeneous mixing of the moderately insensitive explosive precipitated on at least one component of the combustible particle is provided, the other components of the initiator composition are added and mixed.
The compositions of the initiator according to one or more embodiments of the invention do not require additional solvents, although the invention is not limited as such.
As used herein, the term wetted refers to a water content between about 10% by weight and about 50% by weight, more suitably about 15% by weight to about 40% by weight and even more appropriately about 20% by weight, about 30% by weight. In one embodiment, about 25% by weight of water or more is employed, for example, 28% by weight is employed.
If a sensitizer is added, the sensitizer can also be added to the moderately insensitive explosive dampened with water, or to the mixture of moderately insensitive explosive / moistened fuel particles. The sensitizer can optionally include an additional friction generator, such as glass powder.
Although various mechanisms can be employed depending on the explosive component, it is clear that the simple method of mixing water can be used to assemble the compositions of the percussion initiator of the present invention using industry standard practices and such assembly can
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22/36 be carried out safely without stability problems. The use of such a water processing technique is beneficial as previous primer compositions such as MIC-MNC primer compositions have limited stability in water.
The combination of ingredients used in the percussion initiator compositions of the present invention is beneficial because it allows for a simplified processing sequence, in which the micron and oxidant fuel particles do not need to be premixed. The larger oxidant particles used, together with the use of a moderately insensitive secondary explosive, therefore allow a process that is simpler, has an improved safety margin and at the same time reduces the material and the cost of handling. Thus, the invention provides a commercially effective percussion initiator, a result that has so far not been achieved.
Broadly, the explosive composite (moderately insensitive explosive with micro-sized particulate fuel components) in accordance with one or more embodiments of the invention, can be replaced in applications where traditional lead stifinate and diazodinitrophenol (DDNP) initiators and formulations are employed ignition. The explosive composite of the present invention alone is a good ignitor like lead stifinate, where DDNP is absent. The heat output of the explosive composite of the present invention is sufficient to use non-toxic metal oxidizers with higher activation energy typically employed but underused in low flame temperature formulations based on DDNP.
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Additional benefits of the present invention include improved stability, increased ignition capacity, improved ignition reliability, lower cost and increased safety due to the elimination of production and handling of undesirable components, such as lead stifinate and nanometric fuel agents.
The present invention finds use in any igniter or application of the percussion initiator, where lead stifinate is used correctly. For example, the percussion initiator according to the present invention can be used for small and medium caliber cartridges, as well as industrial power cargo, airbags and the like.
The following tables provide various compositions and concentration ranges for a variety of different cartridges. Such compositions and concentration ranges are for illustrative purposes only and are not intended to limit the scope of the present invention.
For the purposes of the following tables, the nitrocellulose component is composed of nitrocellulose fiber in 13.6% by weight nitrogen. Fuel particle component is spherical micron-sized aluminum sold under the trade name Valimet ^TM , which has a normal distribution with the average particle size between 2 and 3 microns, identified in each respective table.
TABLE 1
Illustrative compositions of the pistol percussion initiator
Most appropriate range
Component composition
Appropriate interval
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% by weight % by weight Nitrocellulose 5-25 10-20 Aluminum (2microns) 5-25 6-12 Tetracene 0-10 0-4 Floor propellant 0-20 0-10 Bismuth Trioxide 40-80 50-70 Tragacanth Gum 0-5 0-1
TABLE 2
Illustrative compositions of percussion fusesfor rifle CompositionComponent Appropriate interval% by weight Most appropriate range% by weight Nitrocellulose 5-25 10-20 Aluminum (3 microns) 5-25 6-12 Tetracene 0-10 0-4 Floor propellant 0-20 0-10 Bismuth Trioxide 40-80 50-70 Tragacanth Gum 0-5 0-1
TABLE 3
Illustrative compositions of the percussion initiatorfor rifle Component Composition Appropriate interval% by weight Most appropriate range% by weight Nitrocellulose 5-25 10-20 Aluminum (2 microns) 5-25 6-12
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Tetracene 0-10 0-4 PETN 0-25 0-10 Floor propellant 0-20 0-10 Bismuth Trioxide 40-80 50-70 Tragacanth Gum 0-5 0-1
TABLE 4
Illustrative compositions of the percussion initiatorfor rifle CompositionComponent Appropriate interval% by weight Most appropriate range% by weight Nitrocellulose 5-25 10-20 Aluminum (3 microns) 5-25 6-12 Tetracene 0-10 0-4 Floor propellant 0-20 0-10 Bismuth Trioxide 35-80 55-75 Tragacanth Gum 0-5 0-1
TABLE 5
Illustrative compositions of the percussion initiatorfor shotshell Component Composition Appropriate range% by weight Most appropriate range% by weight Nitrocellulose 5-25 10-20 Aluminum (2 microns) 5-25 6-12 Tetracene 0-10 0-4 PETN 0-25 0-10 Floor propellant 0-20 0-10
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Bismuth Trioxide 40-80 50-70 Tragacanth Gum 0-5 0-1
TABLE 6
Illustrative compositions of the percussion initiatorfor rifle Component Composition Appropriate interval% by weight Most appropriate range% by weight Nitrocellulose 5-25 10-20 Aluminum (3 microns) 5-25 6-12 Tetracene 0-10 0-4 PETN 0-25 0-10 Floor propellant 0-20 0-10 Bismuth Trioxide 35-80 55-75 Tragacanth Gum 0-5 0-1
TABLE 7
Illustrative compositions of the percussion initiatorfor rinfire Component Composition Appropriate interval% by weight Most appropriate range% by weight Nitrocellulose 5-25 6-20 Aluminum (3 microns) 5-25 6-12 Tetracene 0-10 0-4 KDNBF 0-35 0-35 Bismuth Subnitrate 35-80 55-75 Borocylate Glass 0-25 0-15 Tragacanth Gum 0-5 0-1
In one embodiment, the percussion initiator is used in
Petition 870190035589, of 15/04/2019, p. 33/47
27/36 a centerfire gun cartridge, a rimfire gun cartridge or a shotshell. In small arms using the rimfire gun cartridge, a firing pin hits the edge of a gun cartridge case. In contrast, the small arms firing pin, using the centerfire gun cartridge, hits a metal cup in the center of the cartridge case containing the percussion initiator. Nanny cartridges and cartridge cases are known in the art and are therefore not discussed in detail here. The force or impact of the firing pin can produce a percussion event that is sufficient to start the percussion initiator.
Turning now to the figures, Fig. 1A is a longitudinal section of a rimfire gun cartridge shown generally in 6. Cartridge 6 includes a housing 4. Composition of the percussion initiator 2 can be substantially uniformly distributed around an interior volume defined by an edge portion 3 of cartridge housing 4, shown in FIG. 1B, which is an enlarged view of an anterior part of the rimfire 6 gun cartridge shown in Fig. 1 A.
Fig. 2A is a view of the longitudinal section of a centerfire gun cartridge shown generally in 8. As is common with centerfire gun cartridges, FIG. 2A illustrates the assembly of the centerfire percussion initiator 10 in an opening of the housing 4 '. Fig. 2B is an enlarged view of the assembly of the centerfire percussion initiator 10 more clearly showing the composition of the percussion initiator in the assembly of the percussion initiator 10. Centerfire weapon cartridges are known in the art and are therefore not discussed in detail here .
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The propellant composition 12 can be positioned substantially adjacent to the composition of the percussion initiator 2 in the rimfire pistol cartridge 6. In the centerfire weapon cartridge 8, the propellant composition 12 can be positioned substantially adjacent for the assembly of the percussion initiator 10. When ignited or burned, the composition of the percussion initiator 2 can produce sufficient heat and combustion of hot particles to ignite the propellant composition 12 to propel projectile 16 from the firearm barrel or larger caliber ammunition (such as, without limitation, pistol, rifle, automatic rifle, machine gun, any small and medium caliber cartridge, automatic cannon, etc.) in which the 6 or 8 cartridge is discarded. The combustion products of the percussion initiator 2 composition are environmentally friendly, non-toxic, non-corrosive and non-erosive.
As mentioned earlier, the composition of the percussion primer 2 can also be used in larger artillery, such as (without limitation) grenades, mortars or detcord primers, or to start rounds of mortars, rocket engines or other systems, including an explosive secondary, alone or in combination with a propellant, all previous assemblies being encompassed by the term artillery assembly containing initiator, for the sake of convenience. In artillery, the engine or system 14, the combustion of the percussion initiator 2 can be positioned substantially adjacent to a secondary explosive composition 12 in a box 18, as shown in Fig. 3. For the sake of simplicity, as used here, the term artillery must be employed to refer to any
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29/36 one of the aforementioned cartridges, grenades, mortars, starters, rocket engines or any other system in which the percussion initiator disclosed here can be used.
In any of the cartridge assemblies discussed above, the composition of the moistened primer is mixed in a standard mixer set such as Hobart or planetary mixer. Primer cups are loaded as a primer mixture moistened in the cup. An anvil is seated in the loaded cup and the set is then placed in an oven to dry.
In Table 8 below, no additional examples are provided to illustrate the present invention, but in no way is it intended to limit its scope. The letters P, SR, LR, R and SS in relation to each example not limiting denotes different types of ammunition (P refers to pistol cartridges, SR refers to small rifle cartridges, LR refers to large shotgun, R refers to rimfire cartridges and SS refers to shotshells). Each of the supplied components are present in weight percent, and characteristics of the nitrocellulose component and the aluminum fuel particle component are the same provided in the tables above.
TABLE 8
Examples of Composers of the Percussion Initiator Component Ex. 1 Ex.2 Ex.3 Ex.4 Ex.5 Ex.6 Ex.7(P) (SR) (LR) (SR) (SS) (SR) (R) Nitrocellulose 18 15 15 15 15 15 6 Aluminum (2 9 _ _9_
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pm) Aluminum (3pm) - 9 9 9 - 9 5 Tetracene 4 4 2 4 6 4 4 KDNBF - - - - - - 32 PETN - - - - 5 5 - Floor propellant 3 6 6 6 6 6 - TrioxideBismuth 65 65 67 - 60 - - Subnitrate ofBismuth - - - 65 - 60 37 GlassBorosilicate - - - - - - 15 Gumtragacanth 1 1 1 1 1 1 1
An example of making the initiator compositions from examples 1-7 generally includes:
(a) mixing the moistened nitrocellulose component with the aluminum fuel particle component to form the explosive compound;
(b) adding the remaining moistened energy components to the explosive composite and mixture. The remaining moistened-energetic components can include tetracene, floor propellant, KDNBF, PETN and mixtures thereof.
(c) adding the dry mix components to the composition in (b) and mixing until homogeneous to form the compositions of the initiator of the present invention. The dry mix components can include the oxidizing, attracting and binding components.
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Water can also be added in any of the previous steps to adjust the moisture content of the composition mixture. In some embodiments, water is added before the dry components are added to adjust the moisture content before the components are mixed. In some other embodiments, water is added after the dry components are added. Compositions of the initiator of the present invention can also be made by adding the respective components alternating the order of the previous example.
The sensitivity of the primer composition in example 1 was tested with the results provided in table 9. The sensitivity test of the primer composition in Example 1 was conducted according to the small pistol, 9 mm NATO specifications, 54.99 grams projectile / 0.0019 meters of pin diameter. The sensitivity tests of the initiator compositions of Example 2, Example 4 and Example 6 were conducted according to the small rifle, U.S. military specifications, 111.69 grams projectile / 0.0015 meter pin diameter. The sensitivity test of the initiator composition of Example 3 was conducted according to the large rifle, U.S. military specifications, 111.69 grams projectile / 0.0019 meter pin diameter. The cartridge sensitivity test of the initiator composition of Example 5 was performed according to SAAMI.
TABLE 9
Examples of Composers of the Percussion Initiator
Specification (inches) Ex. 1 Ex.2
Ex.3
Ex.4
Ex.5
Ex.6
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All Fire 7 10 9 8 5 7 All Miss 4 6 4 4 2 3 H-bar 5.46 7.50 6.64 5.98 3.14 5.02 Standard deviation 0.72 0.85 1.06 0.64 0.79 0.70 H + 5 9.06 - 11.93 - - - H-2 4.02 - 4.52 - - - H + 3 - 10.05 - 7.90 - 7.12 H-3 - 4.95 - 4.06 - 1.92 H + 4 - - - - 6.32 - H-2 - - - - 1.55 -
For the data in Table 9, the respective specifications also have specification limits. The specification of limits applicable to Example 1 is the standard H + 5 is less than or equal to 0.30 meters, and the standard H-2 is greater than or equal to 0.07 meters. The specification of limits applicable to Example 2, Example 4 and Example 6 is the standard H + 3 is less than or equal to 0.3 0 meters, and with the standard H-3 is greater than or equal to 0.7 0 meters. The specification of limits applicable to Example 3 is the standard H + 5 is less than or equal to 0.38 meters, and with the standard H-2 it is greater than or equal to 0.70 meters. The specification of limits applicable to Example 5 is the standard H + 4 is less than or equal to 0.35 meters, and with the standard H-2 it is greater than or equal to 0.02 meters.
As predicted in the previous sensitivity test data in Table 9, the primer compositions of Examples 1-7 meet the specification criteria for the respective assays.
As shown in Table 10, comparative ballistics data indicates that performance characteristics
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33/36 of the initiator compositions of the present invention, as indicated by speed and pressure, are approximately equal to or better than conventional lead-based stifinate initiators. The moderately low standard deviations of the compositions of the initiators of the present invention also indicate that consistent results are observed. In obtaining comparative ballistic data, control ammunition used military-spec compatible ammunition with a conventional lead-based stifinate primer. The initiator is the only variable between control ammunition and example ammunition, since no adjustments have been made to a standard case, propellant projectile, or propellant charge. In obtaining comparative ballistic data for the starter compositions of the present invention and the respective control starters, the 9 mm NATO specifications were used for the ammunition containing the starter composition of Example 1 and the M882 Control, 5.56 mm of the US military specifications were used for the ammunition containing the composition of the example of Example 2 and Control Ml93, 7.62mm of the US military specifications were used for ammunition containing the composition of the example of Example 3 and Control M80, and SAAMI specification 12 gauge cartridge was used for the ammunition, containing the composition of the Example 5 initiator and Control.
TABLE 10
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Sample velocity Detour-Speed pattern Pressure(psi) Pressure range Timefrom PicoinPressure(ps) Port pressure (psi) (M/ / s) * (Fs) Ex. 1 (smallgun) 390 * 0.7 24.14 3708 241 - Control 1 (M882) 389 * 1 24.66 3893 242 - Ex. 2 (small rifle) 3191 13 57.02 4332 921 16.98 Control 2 (M193) 3132 13 53.28 2575 956 16.89 Ex. 3 (large rifle) 2780 50 55.79 5187 1407 11.17 Control 3 (M80) 2783 37 57.3 4013 1298 11.21 Ex. 5 (cartridge) 1155 35 8150 1196 - - Control 5(cartridge) 1156 16 8581 1049 - -
Table 11 shows the results of thermal stability over time at 79.44 ° C, when tested on a 9 mm cartridge. The control group contains a traditional initiator composition, using lead stifinate as the primary explosive.
TABLE 11
CONTROL EX. 1 Days at 79.44 ⁰ C velocity Pressure velocity Pressure 0 998 33,124 983 32.07 11 987 32.86 1036 37.89 20 966 32,177 1048 39.9 32 959 31,552 1056 40.92
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40 918 29,467 1057 41.49 49 811 22,802 1066 43.24 60 710 13,417 1028 40.97
For the test data in Table 11, all data were obtained under the same conditions, with the composition of the initiator being the only variable between the ammunition of the control group and the ammunition that contains the composition of the initiator of the present invention. In each case, the composition of the initiator according to an embodiment of the present invention is approximately equal to or better than the values of the control group that contains a traditional initiator composition, using lead stifinate as the primary explosive. It should be noted that the values of the composition of the initiator of Example 1 show that the expected ballistic data increases as the moisture and volatiles of the propellant are evaporated, which continues and then stabilizes the higher pressure. This phenomenon is also observed with the control initiator for the common test at 65.55 ° C. Thermal stability at 79.44 ° C has been shown to be a much better indicator than the common test at 65.55 ° C, as it accelerates the potential for interaction and degradation problems of the components of the initiator composition, not necessarily viewed at 65.55 ° C.
As discussed earlier, the present invention finds use in any application in which igniters or percussion initiators are employed. Such applications typically include an igniter or percussion initiator, a secondary explosive, and for some applications, an agent
Petition 870190035589, of 15/04/2019, p. 42/47
36/36 propellant.
As mentioned earlier, other applications include, but are not limited to, igniters for grenades, mortars, fuse starters, mortars, detonators such as rocket engines and mortars, or other systems that include an igniter or igniter , a secondary explosive system, alone or in combination with a propellant, or gas generation systems.
The above disclosure is intended to be illustrative and not exhaustive. This description will suggest many variations and alternatives for anyone skilled in the art without departing from the scope of the present invention. All of these alternatives and variations are intended to be included within the scope of the appended claims. Those familiar with the technique may recognize other equivalents to the specific embodiments described herein that equivalents are also intended to be covered by the appended claims.

权利要求:
Claims (10)
[1]
1. Composition of percussion initiator, characterized by the fact that it comprises:
5 to 40% by weight, based on the dry weight of the initiator composition, of at least one moderately insensitive explosive component, wherein the at least one moderately insensitive explosive component is chosen from nitrocellulose, pentaerythritol tetranitrate (PETN), 2,
4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazatetracyclo [5.5.0.0.5'903'11] dodecane (CL-20), cyclo-l, 3, 5 - trimethylene-2,4,6-trinitramine (RDX), cyclotetramethylene tetranitramine (HMX), 2,4,6-trinitrotoluene (TNT), nitroguanidine, stylic acid, potassium dinitrobenzofuraxane (KDNBF) and mixtures thereof;
5 to 25% by weight, based on the dry weight of the initiator composition, of a plurality of fuel particles with an average particle size of 1.5 microns to 12 microns, devoid of fuel particles with a particle size of 1,000 nanometers or less, in which the plurality of fuel particles is chosen from aluminum, boron, molybdenum, titanium, tungsten, magnesium, melamine, zirconium, calcium silicide or mixtures thereof; and
35 to 80% by weight, based on the dry weight of the initiator composition, of an oxidizing agent, wherein the oxidizing agent is chosen from bismuth trioxide, bismuth subnitrate, bismuth tetroxide, bismuth sulfide, zinc peroxide, tin oxide, manganese dioxide, molybdenum trioxide, potassium nitrate and combinations thereof; where the primary explosive is devoid of a traditional primary explosive containing styphnate of
Petition 870200001155, of 03/01/2020, p. 13/17
[2]
2/4 lead, metallic azides, mercury fulminate, dinitrophenol or mixtures thereof.
2. Percussion initiator composition according to claim 1, characterized by the fact that at least one moderately insensitive explosive comprises nitrocellulose and at least one second moderately insensitive explosive chosen from pentaerythritol tetranitrate (PETN), 2,4 , 6, 8,10,12-hexanitro-
2,4,6,8,10,12-hexaazatetracycle [5.5.0.0. <5.9> 0 <3.11>] dodecane (“CL-20”), cycle -1,3,5-trimethylene-2,4,6trinitramine (RDX), cyclotetramethylene tetranitramine (HMX), 2,4, 6-trinitrotoluene (TNT), nitroguanidine, stylic acid and potassium dinitrobenzofuraxane (KDNBF).
[3]
Percussion initiator composition according to claim 1 or 2, characterized in that it comprises from 8% by weight to 25% by weight of at least one moderately insensitive explosive based on the dry weight of the initiator composition.
[4]
Percussion initiator composition according to any one of claims 1 to 3, characterized in that it comprises 6% by weight to 12% by weight of the plurality of fuel particles based on the dry weight of the initiator composition.
[5]
Percussion initiator composition according to any one of claims 1 to 4, characterized in that the plurality of fuel particles have a spherical shape.
[6]
6. Percussion initiator composition according to any one of claims 1 to 5, characterized by the fact that the plurality of fuel particles has
Petition 870200001155, of 03/01/2020, p. 14/17
3/4 an average particle size of 2 to 9 microns.
[7]
Percussion initiator composition according to any one of claims 1 to 6, characterized in that it further comprises a sensitizer in an amount greater than 0% by weight to 10% by weight, based on the dry weight of the composition of initiator.
[8]
Percussion initiator composition according to any one of claims 1 to 7, characterized in that it further comprises a binder, a ground propellant, an inert filler material or combinations thereof or in which at least one moderately insensitive explosive is nitrocellulose and a second moderately insensitive explosive chosen from pentaerythritol tetranitrate (PETN), 2,4,6,8,10,12-hexanitro-
2,4,6,8,10,12-hexa-azathetracycle [5.5.0.0. 5 '9 03' 11] dodecane (CL-20), cyclo-1, 3,5-trimethylene-2,4,6trinitramine (RDX), cyclotetramethylene tetranitramine (HMX), 2,4,6trinitrotoluene (TNT), nitroguanidine, stific acid and potassium dinitrobenzofuraxane (KDNBF).
[9]
Percussion initiator composition according to any one of claims 1 to 8, characterized in that it is arranged within ammunition chosen from a central cannon cartridge, a rim gun cartridge and a set of ammunition containing initiator.
[10]
10. Method for making the percussion initiator composition, as defined in any of the preceding claims, characterized by the fact that the method comprises:
provide at least one wet explosive in the water, the hair
Petition 870200001155, of 03/01/2020, p. 15/17
4/4 minus a wet explosive in water comprising at least one moderately insensitive explosive; and combining the plurality of fuel particles with at least one wet explosive in the water to form a first mixture.

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法律状态:
2018-04-10| B06F| Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]|

2019-02-12| B06T| Formal requirements before examination [chapter 6.20 patent gazette]|

2019-04-24| B25A| Requested transfer of rights approved|Owner name: VISTA OUTDOOR OPERATIONS LLC (US) |

2019-10-08| B07A| Technical examination (opinion): publication of technical examination (opinion) [chapter 7.1 patent gazette]|

2020-02-18| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|

2020-04-07| B16A| Patent or certificate of addition of invention granted|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 29/03/2011, OBSERVADAS AS CONDICOES LEGAIS. |

优先权:

申请号 | 申请日 | 专利标题

US12/751,607|US8206522B2|2010-03-31|2010-03-31|Non-toxic, heavy-metal free sensitized explosive percussion primers and methods of preparing the same|

PCT/US2011/030315|WO2011123437A2|2010-03-31|2011-03-29|Non-toxic, heavy-metal free sensitized explosive percussion primers and methods of preparing the same|

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