专利摘要:
A propellent charge powder for barrel-type weapons having a plasticizer on the basis of nitramine and nitrocellulose, nitramine and energetic and non-energetic plastic binders, or nitrocellulose or an explosive, and wherein the plasticizer is a mixture of at least two chemically different dinitro diaza compounds. The plasticizer facilitates the production and use of the propellent charge powder possessing a low temperature coefficient.
公开号:US20010003295A1
申请号:US09/355,479
申请日:1998-02-06
公开日:2001-06-14
发明作者:Walter Langlotz;Dietmar Muller
申请人:Diehl Stiftung and Co KG;
IPC主号:C06B25-34
专利说明:
[0001] The invention relates to a propellent charge powder for barrel-type weapons as set forth in the classifying portion of claim [0001] 1.
[0002] DE 35 00 068 C1 concerns a monobasic or polybasic propellent charge powder using 0,0′-dioxy azobenzene for the purposes of improving mechanical properties at down to −55° C. No information is given about temperature coefficients. In addition no diaza compound is used. [0002]
[0003] DE 33 16 676 C2 describes a propellant composition based on nitrocellulose with hexogen, a blasting oil and plasticiser or softener as well as nitroglycerine. No mention is made of a diaza compound however and there is also no information about temperature coefficients. [0003]
[0004] DE 30 33 519 C2 concerns a rocket propellant for a usually low pressure range upon combustion. No information is given about the pressure range which is relevant for propellent charge powder of over 3000 bars. Admittedly, some indications are afforded in regard to mechanical properties in a wide temperature range. There is however no information about temperature coefficients, dependency of the gas pressure on the temperatures of the propellent charge powder. The energetic plasticiser or softener is blasting oil such or Ngl but no diaza compound. [0004]
[0005] A further known propellent charge powder as disclosed in DE 22 60 259 A involves a propellant composition for rockets and not a propellent charge for barrel-type weapons. That propellent charge, like generally all dibasic propellants, is heavily temperature-dependent in the temperature range which is of interest. [0005]
[0006] U.S. Pat. No 4,567,296 A describes an energetic plasticiser or softener on the basis of a fluorine-bearing aza compound. That aza compound, more specifically 1-fluoro-1,1,5-trinitro-3-oxa-5-azahexane is not suitable for use in barrel-type weapons and propellent charge powders. Upon combustion in a weapon, the steel is destroyed, particularly at the usually high pressures and temperatures. In addition that compound gives rise to a major disposal problem. The starting material 2-nitro-2-aza-1 propanol is chemically basically different from a diaza compound. [0006]
[0007] Upon firing munitions with conventional propellent charge powder, the ballistic values maximum pressure and projectile velocity are also heavily temperature-dependent. The pressure and the velocity of 120 mm KE-munition rise from −40° C. to +50° C. by about 1500 bars and 165 m/s, that is to say 10% of the reference or target speed at normal temperature of +21° C. On the basis thereof, on the one hand the armament operational gas pressure cannot be fully utilised at normal temperature, which would result in a high velocity, and on the other hand, because of the only inaccurately known current initial projectile velocity the hit probability is markedly reduced or measures must be taken to ascertain the current projectile velocity in order not to suffer a loss in terms of hit accuracy. [0007]
[0008] The object of the present invention is to propose a propellent charge powder for barrel-type weapons, which has a low temperature coefficient in the temperature range of −50° C. to +70° C. [0008]
[0009] The invention attains that object in accordance with the characterising features of claim [0009] 1. Advantageous developments of the invention are set forth in the appendant claims.
[0010] By virtue of the use of a particular plasticiser or softener the invention makes it possible to produce and use propellent charge powder with a low temperature coefficient. In other words: a propellent charge powder of that kind makes it possible to fire armament munition with almost dibasic propellants, is heavily temperature-dependent in the temperature range which is of interest. [0010]
[0011] U.S. Pat. No. 4,567,296 A describes an energetic plasticiser or softener on the basis of a fluorine-bearing aza compound. That aza compound, more specifically 1-fluoro-1,1,5-trinitro-3-oxa-5-azahexane is not suitable for use in barrel-type weapons and propellent charge powders. Upon combustion in a weapon, the steel is destroyed, particularly at the usually high pressures and temperatures. In addition that compound gives rise to a major disposal problem. The starting material 2-nitro-2-aza-1 propanol is chemically basically different from the dinitro diaza compounds according to the invention. [0011]
[0012] A better plasticisable propellent charge powder, in accordance with U.S. Pat. No. 4,457,791, is based on a plasticiser DMMD. Further plasticisers as additives to that specified are not provided. There is no indication that the temperature coefficient upon combustion is positively influenced. [0012]
[0013] Transformation or the gas-generation rate of conventional monobasic and polybasic propellent charge powders is highly temperature-dependent. The greater the initial powder temperature, that much faster is combustion of the propellent charge powder. That property is substance-specific and can be described for example to a good degree of approximation by the combustion law as follows: [0013] γ = β · ( p p 0 ) a ·  τ     T
[0014] with T as the temperature of the propellent charge powder. In that equation τ denotes the so-called temperature coefficient of the propellent charge powder, which is of different values for the various powder compositions and which represents a substance constant. In addition γ denotes the velocity with which the combustion front progresses, β and α represent substance constants and p is the pressure under which the propellent charge powder is, wherein p[0014] o is atmospheric pressure.
[0015] As a result of the temperature-dependency of the combustion speed of the propellent charge powder, the maximum gas pressure which occurs when firing munition with conventional monobasic and polybasic propellent charge powder from an armament, in the charge chamber of the weapon, and thus also the projectile launch velocity are also severely temperature-dependent. [0015]
[0016] The pressure and the velocity of 120 mm KE-munition rise from −40° C. to +50° C. by about 1500 bars and 165 m/s, that is to say 10% of the reference or target speed at normal temperature of +21° C. On the basis thereof, on the one hand the armament operational gas pressure cannot be fully utilised at normal temperature, which would result in a high velocity, and on the other hand, because of the only inaccurately known current powder temperature and thus the initial projectile velocity the hit probability is markedly reduced or measures must be taken to ascertain the current projectile velocity in order not to suffer a loss in terms of hit accuracy. [0016]
[0017] The object of the present invention is to propose a propellent charge powder for barrel-type weapons, which has a low temperature coefficient in the temperature range of −50° C. to +70° C. so that in that way the specified ballistic values of maximum pressure and projectile velocity depend only slightly on the powder temperature. [0017]
[0018] The invention attains that object in accordance with the characterising features of claim [0018] 1. Advantageous developments of the invention are set forth in the appendant claims.
[0019] By virtue of the use of a particular plasticiser or softener the invention makes it possible to produce and use propellent charge powder with a low temperature coefficient. In other words: a propellent charge powder of that kind makes it possible to fire armament munition with almost constant values in respect of maximum pressure and projectile velocity in the entire temperature range of −50° C. to +70° C. [0019]
[0020] Embodiments of the invention are set out hereinafter, a diagram illustrating the temperature characteristics of a conventional propellent charge powder and a propellent charge powder according to the invention. [0020]
[0021] The invention concerns the following propellent charge powders: [0021]
[0022] glycidyl azide polymer (GAP)—, [0022]
[0023] hydroxy-terminated polybutadiene (HTPB), polybutadiene with terminal hydroxyl groups— and [0023]
[0024] cellulose acetate butyrate (CAB)— [0024]
[0025] bound nitramine propellent charge powders with the dinitro diaza plasticiser mixture according to the invention and nitrocellulose propellent charge powders, NC, which comprise nitramines, nitrocellulose and dinitro diaza plasticiser or nitrocellulose and dinitro diaza plasticiser with or without blasting oil such as nitroglycerine (Ngl) or diglycol dinitrate (DEGN). [0025] PCP-formulation % by weightRDX or HMX 70 ± 15 70 ± 15 70 ± 15 40 ± 15 60 ± 20 40 ± 15 Plasticiser DNDA- 10 ± 8  10 ± 8  15 ± 10 30 ± 25 20 ± 12 30 ± 25 mix (3 components) GAP with isocyanate 20 ± 5  GAP without 30 ± 20 isocyanate HTPB with  20 ± 5 isocyanate CAB 15 ± 5  NC + stick 30 ± 5  20 ± 12 70 ± 25 30 ± 15 blasting oil 0 + 40
[0026] The abbreviations RDX=hexogen and HMX=octogen, while PCP is used to mean propellent charge powder. [0026]
[0027] With nitratoethyl nitramine (NENA), poly-3-nitratomethyl-3′ -methyloxetan (PolyNIMMO) and poly-glycidyl nitrate ester (Polyglyn) as energetic polymer binder, a comparable temperature behaviour occurs insofar as the plasticiser according to the invention is used in the above-specified quantitative proportion. In the case of Polyglyn the azide group of GAP is replaced by —O—NO[0027] 2.
[0028] The dinitro diaza plasticiser comprises the following components: [0028]
[0029] 2,4-Dinitro-2,4-diazapentane 40±10% by weight [0029]
[0030] 2,4-Dinitro-2,4-diazahexane 45±10% by weight [0030]
[0031] 3,5-Dinitro-3,5-diazaheptane 15±15% by weight [0031]
[0032] The diagrammatically illustrated graph sets out the pressure configuration on the orinate 2 when the weapon is fired in relation to the temperature on the abscissa 1. [0032]
[0033] In the case of a propellent charge powder in accordance with the state of the art the pressure changes very severely in the specified temperature range of −50° C. to +70° C. in accordance with the rising curve 5. [0033]
[0034] In comparison the pressure remains almost constant as indicated by the curve 6 in the specified temperature range. The curve 6 initially rises and then falls somewhat from the reversal point 7. The optimum is an almost horizontal configuration corresponding to the curve 15. [0034]
[0035] If the propellent charge powder in accordance with the invention is altered by conventional measures such as altering the grain geometry in such a way that the original curve 6 lies as curve 6.1 with its reversal point 7.1 against the pressure limit 10, that denotes a considerable increase in power or performance of 10 to 20% with respect to the usual propellent charge powder as indicated by curve 5. [0035]
权利要求:
Claims (9)
[1" id="US-20010003295-A1-CLM-00001] 1. A propellent charge powder for barrel-type weapons having a plasticiser on the basis of
nitramine such as RDX, HMX and nitrocellulose,
nitramine and energetic and non-energetic plastic binders, or
nitrocellulose, or
an explosive, such as CL-20
characterised in that the plasticiser is a mixture of at least three chemically different dinitro diaza compounds.
[2" id="US-20010003295-A1-CLM-00002] 2. A propellent charge powder as set forth in
claim 1 characterised in that the plasticiser comprises the following components:
4-Dinitro-2,4-diazapentane 40±10% by weight
2,4-Dinitro-2,4-diazahexane 45±10% by weight
3,5-Dinitro-3,5-diazaheptane 15±15% by weight
[3" id="US-20010003295-A1-CLM-00003] 3. A propellent charge powder as set forth in
claim 1 . characterised in that the proportion of plasticiser in the propellent charge powder is between 2 and 55% by weight.
[4" id="US-20010003295-A1-CLM-00004] 4. A propellent charge powder as set forth in
claim 1 or
claim 2 characterised in that the plasticiser comprises dinitro diaza alkanes, dinitro diaza alkenes or dinitro diaza alkines or a mixture thereof.
[5" id="US-20010003295-A1-CLM-00005] 5. A propellent charge powder as set forth in one of
claims 1 to
4 characterised in that it contains stabilisers or stabilisers and combustion moderators.
[6" id="US-20010003295-A1-CLM-00006] 6. A propellent charge powder as set forth in one or more of claims 1 through 5 characterised in that besides the dinitro diaza compound it additionally contains still other energetic or non-energetic plasticisers such as methy-nena, ethyl-nena or butyl-nena.
[7" id="US-20010003295-A1-CLM-00007] 7. A propellent charge powder as set forth in
claim 1 or
claim 6 characterised in that the following can be used as energetic binders:
poly-3-nitratomethyl-3-methyloxetan (PolyNIMMO),
poly-glycidyl nitrate ester (Polyglyn)
glycidyl azide polymer (GAP)
poly-3-azidomethyl-3′-methyloxetan (AMMO),
poly-3,3′-bis-azidomethyloxetan (BAMO)
or a mixture thereof.
[8" id="US-20010003295-A1-CLM-00008] 8. A propellent charge powder as set forth in
claim 1 or
claim 6 characterised in that the non-energetic binders are polybutadiene with terminal hydroxyl groups (HTPB), cellulose acetate butyrate (CAB) or a mixture thereof.
[9" id="US-20010003295-A1-CLM-00009] 9. A propellent charge powder as set forth in one or more of claims 1 through 8 characterised in that the explosive comprises 1,3,3-trinitroazetidine (TNAZ), ammonium dinitramide (AND), triaminoguanidine nitrate (TAGN) or hexanitro-hexa-aza-iso-wurtzitan (CL-20) or a mixture thereof.
类似技术:
公开号 | 公开日 | 专利标题
US6309484B2|2001-10-30|Propellent charge powder for barrel-type weapons
US9199887B2|2015-12-01|Propellant compositions including stabilized red phosphorus and methods of forming same
US5468313A|1995-11-21|Plastisol explosive
US6682615B2|2004-01-27|Insensitive high energy booster propellant
US4938813A|1990-07-03|Solid rocket fuels
JP3370118B2|2003-01-27|Stable solid rocket propellant composition
US5716557A|1998-02-10|Method of making high energy explosives and propellants
US4216039A|1980-08-05|Smokeless propellant compositions having polyester or polybutadiene binder system crosslinked with nitrocellulose
US6024810A|2000-02-15|Castable double base solid rocket propellant containing ballistic modifier pasted in an inert polymer
US6783614B1|2004-08-31|Minimum signature propellant
US5798481A|1998-08-25|High energy TNAZ, nitrocellulose gun propellant
US3732131A|1973-05-08|Gun propellant containing nitroplasticized nitrocellulose and triaminoguanidine nitrate
WO1995009824A1|1995-04-13|Bamo/ammo propellant formulations
US3834956A|1974-09-10|Solid propellant composition containing lead and lead compounds
Finck et al.1996|New molecules for high energetic materials
US6217682B1|2001-04-17|Energetic oxetane propellants
DE19757469C2|2000-11-02|Propellant powder for guns
US6997996B1|2006-02-14|High energy thermoplastic elastomer propellant
US6673174B2|2004-01-06|High performance plastic bonded explosive
US9759162B1|2017-09-12|Controlled autoignition propellant systems
US6126763A|2000-10-03|Minimum smoke propellant composition
Szala2020|Development trends in artillery ammunition propellants
Szala2020|Review/Przegląd Development trends in artillery ammunition propellants Analiza możliwości eliminacji nitrocelulozy z materiałów wybuchowych miotających
US6066213A|2000-05-23|Minimum smoke propellant composition
Boileau1995|Overview on energetic polymers
同族专利:
公开号 | 公开日
AU6395098A|1998-08-26|
EP0960083A1|1999-12-01|
US6309484B2|2001-10-30|
WO1998034891A1|1998-08-13|
AU719937B2|2000-05-18|
EP0960083B1|2004-08-25|
CA2280029A1|1998-08-13|
CA2280029C|2006-06-06|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题
US20060195077A1|2002-10-21|2006-08-31|Advanced Medical Optics Inc.|System and method for pulsed ultrasonic power delivery employing cavitational effects|
US20060200068A1|2002-10-21|2006-09-07|Advanced Medical Optics, Inc.|Novel enhanced microburst ultrasonic power delivery system and method|
US20070073309A1|1997-01-22|2007-03-29|Advanced Medical Optics, Inc.|Control of pulse duty cycle based upon footswitch displacement|
DE102005037017B4|2005-08-05|2007-09-27|Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V.|Powder preconcentrate and its use|
US20100114010A1|2006-08-01|2010-05-06|Abbott Medical Optics Inc.|Vacuum sense control for phaco pulse shaping|
US20100276042A1|2004-03-15|2010-11-04|Alliant Techsystems Inc.|Reactive compositions including metal|
US7857783B2|1997-01-22|2010-12-28|Abbott Medical Optics Inc.|Micro-burst ultrasonic power delivery|
US8020565B2|2002-10-21|2011-09-20|Abbott Medical Optics, Inc.|Modulated pulsed ultrasonic power delivery system and method|
US9050627B2|2011-09-02|2015-06-09|Abbott Medical Optics Inc.|Systems and methods for ultrasonic power measurement and control of phacoemulsification systems|
US9103641B2|2000-02-23|2015-08-11|Orbital Atk, Inc.|Reactive material enhanced projectiles and related methods|
US20160052836A1|2013-03-27|2016-02-25|Bae Systems Plc|Non-phthalate propellants|US2978495A|1955-08-22|1961-04-04|Aerojet General Co|Nitramino esters|
GB963336A|1959-10-01|1964-07-08|Aerojet General Co|Method for preparing secondary nitramines|
US4002514A|1965-09-30|1977-01-11|The Dow Chemical Company|Nitrocellulose propellant composition|
US3873579A|1969-08-20|1975-03-25|Us Navy|Organic azides and method of preparation thereof|
US3697341A|1969-08-29|1972-10-10|Hercules Inc|Cool burning smokeless powder composition containing nitramine ethers|
US4085123A|1976-10-21|1978-04-18|Rockwell International Corporation|1,3-Diazido-2-nitrazapropane|
US4216039A|1978-11-20|1980-08-05|The United States Of America As Represented By The Secretary Of The Army|Smokeless propellant compositions having polyester or polybutadiene binder system crosslinked with nitrocellulose|
DE2900020C2|1979-01-02|1982-12-09|WNC-Nitrochemie GmbH, 8261 Aschau|Process for the production of a polybasic propellant charge powder|
US4432817A|1982-03-25|1984-02-21|The United States Of America As Represented By The Secretary Of The Air Force|Propellant containing an azidonitrocarbamate plasticizer|
US4482404A|1982-04-08|1984-11-13|The United States Of America As Represented By The Secretary Of The Air Force|Azido nitramino ether containing solid propellants|
US4457791A|1982-06-25|1984-07-03|The United States Of America As Represented By The Secretary Of The Navy|New plasticizer for nitropolymers|
US4476322A|1982-07-01|1984-10-09|The United States Of America As Represented By The Secretary Of The Navy|Synthesis of dimethylmethylene dinitramine|
US5186770A|1984-06-29|1993-02-16|The United States Of America As Represented By The Secretary Of The Navy|Bis ether|
US4567296A|1984-06-29|1986-01-28|The United States Of America As Represented By The Secretary Of The Navy|1-Fluoro-1,1,5-trinitro-3-oxa-5-azahexane and method of preparation|
US4614800A|1985-02-15|1986-09-30|The United States Of America As Represented By The Secretary Of The Navy|Synthesis of cyclic dinitramines useful as explosive and propellant ingredients, gas generants and in other ordnance applications|
US4761250A|1985-08-09|1988-08-02|Rockwell International Corporation|Process for preparing 1,5-diazido-3-nitrazapentane|
US5482581A|1988-08-25|1996-01-09|Ici Explosives Usa Inc.|Low vulnerability propellant plasticizers|
US5053087A|1990-03-02|1991-10-01|Rockwell International Corporation|Ultra high-energy azide containing gun propellants|
US5529649A|1993-02-03|1996-06-25|Thiokol Corporation|Insensitive high performance explosive compositions|
US5695216A|1993-09-28|1997-12-09|Bofors Explosives Ab|Airbag device and propellant for airbags|
US5487851A|1993-12-20|1996-01-30|Thiokol Corporation|Composite gun propellant processing technique|
DE4435524C2|1994-10-05|1996-08-22|Fraunhofer Ges Forschung|Solid fuel based on pure or phase-stabilized ammonium nitrate|
US5587553A|1994-11-07|1996-12-24|Thiokol Corporation|High performance pressable explosive compositions|
US5798481A|1995-11-13|1998-08-25|The United States Of America As Represented By The Secretary Of The Army|High energy TNAZ, nitrocellulose gun propellant|DE10020020A1|2000-04-22|2001-10-25|Tzn Forschung & Entwicklung|cartridge|
US20090208647A1|2000-06-15|2009-08-20|Nitrochemie Wimmis Ag|Method for producing a funtional, high-energy material|
ES2235813T3|2000-06-15|2005-07-16|Nitrochemie Wimmis Ag|PROCEDURE FOR THE MANUFACTURE OF A HIGHLY ENERGETIC FUNCTIONAL MATERIAL.|
FR2850376B1|2003-01-29|2007-02-16|Saint Louis Inst|PLASTICIZER FOR PROPULSIVE POWDER WITH INDEPENDENT COMBUSTION OF AMBIENT TEMPERATURE|
DE102010020776B4|2010-05-18|2015-03-05|Diehl Bgt Defence Gmbh & Co. Kg|Propellant charge and method for its production|
法律状态:
1999-07-30| AS| Assignment|Owner name: DIEHL STIFTUNG & CO., GERMANY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LANGLOTZ, WALTER;MULLER, DIETMAR;REEL/FRAME:010176/0532;SIGNING DATES FROM 19990722 TO 19990729 |
2001-10-11| STCF| Information on status: patent grant|Free format text: PATENTED CASE |
2005-05-02| FPAY| Fee payment|Year of fee payment: 4 |
2009-04-30| FPAY| Fee payment|Year of fee payment: 8 |
2013-02-28| FPAY| Fee payment|Year of fee payment: 12 |
优先权:
申请号 | 申请日 | 专利标题
DE19704792||1997-02-08||
DE19704792.0||1997-02-08||
DE19704792||1997-02-08||
DE19757469A|DE19757469C2|1997-02-08|1997-12-23|Propellant powder for guns|
DE19757469||1997-12-23||
PCT/DE1998/000639|WO1998040858A1|1997-03-11|1998-02-28|Switch cabinet with a fire extinguishing system|
[返回顶部]