JPS6317798B2 - - Google Patents
Info
- Publication number
- JPS6317798B2 JPS6317798B2 JP53040444A JP4044478A JPS6317798B2 JP S6317798 B2 JPS6317798 B2 JP S6317798B2 JP 53040444 A JP53040444 A JP 53040444A JP 4044478 A JP4044478 A JP 4044478A JP S6317798 B2 JPS6317798 B2 JP S6317798B2
- Authority
- JP
- Japan
- Prior art keywords
- tetracene
- lead
- igniter
- puncture
- particle size
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 claims description 35
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 27
- 150000004767 nitrides Chemical class 0.000 claims description 24
- 238000004200 deflagration Methods 0.000 claims description 19
- 239000002245 particle Substances 0.000 claims description 17
- 239000002360 explosive Substances 0.000 claims description 14
- IWOUKMZUPDVPGQ-UHFFFAOYSA-N barium nitrate Chemical compound [Ba+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O IWOUKMZUPDVPGQ-UHFFFAOYSA-N 0.000 claims description 8
- 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 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
- LTNRJUDZKFOCFJ-UHFFFAOYSA-N 1-nitropentan-2-one Chemical compound CCCC(=O)C[N+]([O-])=O LTNRJUDZKFOCFJ-UHFFFAOYSA-N 0.000 claims description 4
- WETZJIOEDGMBMA-UHFFFAOYSA-L lead styphnate Chemical compound [Pb+2].[O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C([O-])=C1[N+]([O-])=O WETZJIOEDGMBMA-UHFFFAOYSA-L 0.000 claims description 4
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 3
- YLQNPPWBEQCYON-UHFFFAOYSA-N n-[(2,3,4-trinitrophenyl)methyl]nitramide Chemical compound [O-][N+](=O)NCC1=CC=C([N+]([O-])=O)C([N+]([O-])=O)=C1[N+]([O-])=O YLQNPPWBEQCYON-UHFFFAOYSA-N 0.000 claims description 2
- JRLDUDBQNVFTCA-UHFFFAOYSA-N antimony(3+);trinitrate Chemical compound [Sb+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JRLDUDBQNVFTCA-UHFFFAOYSA-N 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 230000002269 spontaneous effect Effects 0.000 description 10
- 230000035945 sensitivity Effects 0.000 description 9
- 239000000843 powder Substances 0.000 description 7
- AGUIVNYEYSCPNI-UHFFFAOYSA-N N-methyl-N-picrylnitramine Chemical compound [O-][N+](=O)N(C)C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O AGUIVNYEYSCPNI-UHFFFAOYSA-N 0.000 description 3
- 229940007424 antimony trisulfide Drugs 0.000 description 3
- NVWBARWTDVQPJD-UHFFFAOYSA-N antimony(3+);trisulfide Chemical compound [S-2].[S-2].[S-2].[Sb+3].[Sb+3] NVWBARWTDVQPJD-UHFFFAOYSA-N 0.000 description 3
- 230000033228 biological regulation Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000028 HMX Substances 0.000 description 1
- TZRXHJWUDPFEEY-UHFFFAOYSA-N Pentaerythritol Tetranitrate Chemical compound [O-][N+](=O)OCC(CO[N+]([O-])=O)(CO[N+]([O-])=O)CO[N+]([O-])=O TZRXHJWUDPFEEY-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 238000009529 body temperature measurement Methods 0.000 description 1
- 229910021346 calcium silicide Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005474 detonation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- RLJMLMKIBZAXJO-UHFFFAOYSA-N lead nitrate Chemical compound [O-][N+](=O)O[Pb]O[N+]([O-])=O RLJMLMKIBZAXJO-UHFFFAOYSA-N 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- XAMUDJHXFNRLCY-UHFFFAOYSA-N phenthoate Chemical compound CCOC(=O)C(SP(=S)(OC)OC)C1=CC=CC=C1 XAMUDJHXFNRLCY-UHFFFAOYSA-N 0.000 description 1
- WVULZDFWPQCPPJ-UHFFFAOYSA-N potassium;hydrochloride Chemical compound Cl.[K] WVULZDFWPQCPPJ-UHFFFAOYSA-N 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B35/00—Compositions containing a metal azide
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明はトリニトロフエニルメチルニトロアミ
ン(テリトル)、ニトロペンタノン(ニトロペン
タ)、トリメチレントリニトロアミン(ヘキソー
ゲン)、テトラメチレンテトラニトラミン(オク
トーゲン)、窒化鉛の何れかの物質及びこれらか
ら成る混合剤を含有する第2次爆薬を点火するた
めに使用可能であり、その場合2〜8重量%のテ
トラセンと98〜92重量%の窒化鉛又は他の成分と
を含有している刺突に敏感な点火薬混合剤に関す
る。Detailed Description of the Invention (Industrial Field of Application) The present invention relates to trinitrophenylmethyl nitramine (teritor), nitropentanone (nitropenta), trimethylene trinitramine (hexogen), tetramethylenetetranitramine (octogen) , lead nitride, and mixtures thereof, in which case 2 to 8% by weight of tetracene and 98 to 92% by weight of lead nitride or and other ingredients.
(従来の技術)
この種の公知の刺突に敏感な点火薬混合剤は2
〜8%のテトラセンを含有する窒化鉛を含んでい
る。このような点火薬混合剤は、トリニトロフエ
ニルメチルニトロアミン、ニトロペンタノン、ト
リメチレントリニトロアミン、テトラメチレンテ
トラニトラミン、窒化鉛のような第2次爆薬を起
爆する作用を有するという利点を有している。し
かるにこのようなテトラセン含有の点火薬混合剤
の欠点は、テトラセンの爆燃温度に相当する、
140℃という低い爆燃温度にある。このような点
火薬混合剤を有する雷管はいわゆる自然発火に対
する安全規定を充足しない。(Prior Art) Known puncture-sensitive igniter mixtures of this type are
Contains lead nitride containing ~8% tetracene. Such igniter mixtures have the advantage of detonating secondary explosives such as trinitrophenylmethylnitroamine, nitropentanone, trimethylenetrinitramine, tetramethylenetetranitramine, lead nitride. are doing. However, the drawback of such tetracene-containing igniter mixtures is that the deflagration temperature of tetracene is
It has a low deflagration temperature of 140℃. Detonators with such ignition powder mixtures do not meet the safety regulations against so-called spontaneous ignition.
旋回弾丸用の雷管は次のような厳重な安全規定
に適合しなければならない。 Detonators for orbiting projectiles must meet strict safety regulations, including:
(a) 雷管は発火器の安全状態において機械的防壁
によつて弾丸の有効爆薬は直接的起爆線から分
離されなければならない。(a) The detonator shall, in the safe condition of the igniter, separate the effective explosive charge of the projectile from the direct detonating cord by a mechanical barrier.
(b) 雷管は高い刺突感度を有さなければならな
い。(b) The detonator shall have high piercing sensitivity.
(c) 雷管は自然発火に対して安全でなければなら
ない、換言すれば兵器の機能故障に際して射撃
で過熱された銃砲身中に弾薬筒が滞留している
時にその発射薬が熱伝導により点火する前に爆
発してはならない。従つて雷管は少なくとも30
分間200℃以上の温度に耐えなければならな
い。。(c) The detonator must be safe against spontaneous ignition, i.e., the propellant charge ignites by conduction while the cartridge is lodged in the overheated gun barrel in the event of a malfunction of the weapon. Do not explode before. Therefore, there are at least 30 detonators
Must withstand temperatures of 200℃ or more for minutes. .
(d) 雷管は点火器の安全位置においてその不慮の
発火に際して尾筒の外周から見える破壊を起こ
してはならない。(d) The detonator shall not cause any damage visible from the outer periphery of the transition tube upon its accidental ignition in the safe position of the igniter.
いわゆる安全規定を充足しかつ前記欠点を有
さない点火薬混合剤は本発明によれば、粒度が
10μm以上、40μm以下のテトラセンが80%の
割合を有する。 According to the invention, the ignition powder mixture which satisfies the so-called safety regulations and does not have the above-mentioned drawbacks has a particle size of
Tetracene with a diameter of 10 μm or more and 40 μm or less accounts for 80%.
テトラセンの粒度が10μm以上、40μm以下で
ある、かかる点火薬混合剤は各種の方法で、例え
ば粉砕、篩粉又は沈澱によつて製造されることが
できる。この点火薬混合剤を製造する本発明によ
る方法は粒度が10μm以上、40μm以下であるテ
トラセン結晶の沈澱を特徴とする。 Such igniter mixtures in which the particle size of the tetracene is greater than or equal to 10 μm and less than or equal to 40 μm can be produced in various ways, for example by grinding, sieving or precipitation. The process according to the invention for producing this igniter mixture is characterized by the precipitation of tetracene crystals with a particle size of 10 μm or more and 40 μm or less.
この種の公知の雷管は、第1に刺突板で被われ
た刺突に敏感な点火薬混合剤、並びに第2に起爆
薬及び第2次爆薬から成る爆薬を有する雷管体を
有している。優先的には第2次爆薬から成る爆薬
の上へは軽金属又は鋼から成る覆板が載せられ、
覆板は縁曲げによつて固定されかつ被覆塗料によ
り密封される。 Known detonators of this type have a detonator body with firstly a puncture-sensitive igniter mixture covered with a puncture plate and secondly an explosive charge consisting of a prime charge and a secondary explosive charge. . A cover plate of light metal or steel is placed over the explosive, which is preferentially a secondary explosive;
The cover plate is secured by edge bending and sealed with a coating material.
3成分、即ち刺突敏感な点火薬混合剤、起爆薬
及び第2次爆薬から成る爆薬を有するかかる雷管
はその製造が多費用である。 Such detonators, which have a three-component explosive charge consisting of a puncture-sensitive igniter mixture, a detonator and a secondary explosive, are expensive to manufacture.
従つて刺突に敏感な点火薬混合剤と第2次爆薬
から成る爆薬だけを有し起爆薬を有していない雷
管も既に公知である。このような雷管のために
は、一方では第2次爆薬を発火できるけれども他
方では自然発火に対して安全ではないという既述
の利点と欠点とを有する窒化鉛と、2〜8%のテ
トラセンとを含有する点火薬混合剤が使用され
る。このような雷管は、その製造において、単に
2個の配量と2回の圧搾とだけを必要とするとい
う利点を有し、このことは3要素雷管に比してそ
の製造を著しく安価にしかつ簡単にする。 Therefore, detonators are already known which contain only an explosive consisting of a puncture-sensitive igniter mixture and a secondary explosive, but without a primer. For such detonators, lead nitride, which has the already mentioned advantages and disadvantages of being able to ignite secondary explosives on the one hand, but not being safe against spontaneous ignition, on the other hand, and 2-8% tetracene are used. An ignition powder mixture containing . Such a detonator has the advantage that, in its manufacture, only two meterings and two squeezes are required, which makes its manufacture significantly cheaper and more efficient than three-element detonators. Make it easy.
本発明による点火薬混合剤を雷管に使用する場
合、雷管体の中に刺突に敏感な本発明による点火
薬混合剤を20〜50%と残りは窒化鉛、トリニトロ
フエニルメチルニトロアミン、ニトロペンタノ
ン、トリメチレントリニトロアミン、テトラメチ
レンテトラニトラミン、窒化鉛の第2次爆薬とが
含まれており、かつこの雷管体は最大限4〜5mm
の直径と5〜6mmの長さとを有することを特徴と
する。 When the igniter mixture according to the invention is used in a detonator cap, 20 to 50% of the igniter mixture according to the invention which is sensitive to puncture is contained in the detonator body and the remainder is lead nitride, trinitrophenylmethyl nitramine, nitropene. Contains secondary explosives such as tanone, trimethylenetrinitramine, tetramethylenetetranitramine, and lead nitride, and this detonator body has a maximum diameter of 4 to 5 mm.
It is characterized by having a diameter of 5 to 6 mm and a length of 5 to 6 mm.
以下若干数の実施例によつて本発明を詳述す
る。 The present invention will be explained in detail below with reference to some examples.
実験目的のため次の点火薬混合剤が製造されか
つ適当な雷管体を炉内で加熱して実験された。温
度測定には電気的温度計等が使用された。爆燃温
度は爆発の瞬間の炉内温度測定により間接的に把
握され、そして雷管は上記の寸法のものが使用さ
れた。尚粒度は直径をμmで表す。 For experimental purposes, the following igniter mixtures were prepared and tested by heating appropriate detonator bodies in a furnace. An electric thermometer etc. was used for temperature measurement. The deflagration temperature was determined indirectly by measuring the temperature inside the reactor at the moment of detonation, and the detonator was of the above dimensions. The particle size is expressed in terms of diameter in μm.
(1) 窒化鉛:95%、テトラセン;5%、粒度;
100μm以上、爆燃温度:約140℃
(2) 窒化鉛:97.5%、テトラセン:2.5%、粒
度:100μm以上、爆燃温度:140℃
(3) 窒化鉛:95%、テトラセン:5%、10μm<
粒度<40μm
(4) 窒化鉛:93%、テトラセン:7%、10μm<
粒度<40μm、爆燃温度:約320℃
(5) 窒化鉛:91%、テトラセン:9%、10μm<
粒度<40μm、爆燃温度:約150℃
(6) 鉛トリニトロレゾルシナート(鉛トリシネー
ト)、硝酸バリウム、三硫化アンチモン、カー
ボランダム:95%、テトラセン:5%、粒度:
100μmより大、爆燃温度:約150℃
(7) 鉛トリニトロレゾルシナート40%、窒化鉛20
%、硝酸バリウム20%、三硫化アンチモン13
%、カーボランダム2%、テトラセン5%、
10μm<粒度<40μm爆燃温度:200℃より大
(8) 2.5%のテトラセン10μm<粒度<40μmと
97.5%の窒化鉛とから成る23%の刺突点火薬、
77%の窒化鉛、自然発火温度:200℃より大
(9) 2.5%のテトラセン、10μm<粒度<40μmと
97.5%の窒化鉛とから成る50%の刺突点火薬、
50%の窒化鉛、自然発火温度:200℃より大
(10) 2.5%のテトラセン、10μm<粒度<40μmと
97.5%の窒化鉛とから成る58.8%の刺突点火
薬、41.5%の窒化鉛、自然発火温度:200℃よ
り小
これらの実験によると、テトラセンが頗る細い
形とかつ充分な分布とによつて使われる場合に自
然発火に対して安全なテトラセン含有の点火薬混
合剤が製造されることが示された。(1) Lead nitride: 95%, tetracene: 5%, particle size;
100μm or more, deflagration temperature: approximately 140℃ (2) Lead nitride: 97.5%, tetracene: 2.5%, particle size: 100μm or more, deflagration temperature: 140℃ (3) Lead nitride: 95%, tetracene: 5%, 10μm<
Particle size <40μm (4) Lead nitride: 93%, tetracene: 7%, 10μm<
Particle size <40μm, deflagration temperature: approx. 320℃ (5) Lead nitride: 91%, tetracene: 9%, 10μm<
Particle size <40μm, deflagration temperature: approx. 150℃ (6) Lead trinitroresorcinate (lead tricinate), barium nitrate, antimony trisulfide, carborundum: 95%, tetracene: 5%, particle size:
Larger than 100μm, deflagration temperature: approx. 150℃ (7) 40% lead trinitroresorcinate, 20% lead nitride
%, barium nitrate 20%, antimony trisulfide 13
%, carborundum 2%, tetracene 5%,
10μm<particle size<40μm Deflagration temperature: greater than 200℃(8) 2.5% tetracene 10μm<particle size<40μm
97.5% lead nitride and 23% piercing igniter, consisting of
77% lead nitride, autoignition temperature >200°C (9) 2.5% tetracene, with particle size < 40 μm < 10 μm
97.5% lead nitride and 50% piercing igniter, consisting of
50% lead nitride, autoignition temperature >200°C (10) 2.5% tetracene, with particle size < 40 μm < 10 μm
58.8% piercing ignition powder consisting of 97.5% lead nitride, 41.5% lead nitride, spontaneous ignition temperature: less than 200°C. These experiments show that tetracene, due to its predominant narrow shape and well-distributed distribution, It has been shown that tetracene-containing igniter mixtures can be produced that are safe against spontaneous ignition when used.
このような点火薬混合剤は雷管の中に配置され
て高度の刺突敏感性を有しかつ特にトリニトロフ
エニルメチルニトロアミン、ニトロペンタノン、
トリメチレントリニトロアミン、テトラメチレン
テトラニトラミン、窒化鉛から成る第2次爆薬の
起爆に適している。しかしながら窒化鉛中の許容
テトラセン含有量と雷管中の点火薬混合剤の全量
には限度がある。例えば2.5%のテトラセンと
97.5%の窒化鉛とから成る点火薬混合剤を有する
雷管が製造される場合、点火薬混合剤の割合は全
量の50%り多くなつてはならない、そうでないと
自然発火安全性が保証されていない。他面、この
点火薬混合剤は例えば8%よりも大きいテトラセ
ン含有量を有してはならない、すなわちテトラセ
ンの更に大きな含有量によつては自然発火安全性
が保証されていないからてある。 Such igniter mixtures are placed in the detonator and have a high degree of puncture sensitivity and contain especially trinitrophenylmethyl nitramine, nitropentanone,
Suitable for detonating secondary explosives consisting of trimethylenetrinitramine, tetramethylenetetranitramine, and lead nitride. However, there are limits to the permissible tetracene content in lead nitride and the total amount of igniter mixture in the detonator. For example, with 2.5% tetracene
If the detonator is manufactured with an ignition mixture consisting of 97.5% lead nitride, the proportion of the ignition mixture must not be more than 50% of the total amount, otherwise the spontaneous ignition safety is guaranteed. do not have. On the other hand, the igniter mixture must not have a tetracene content of more than 8%, for example, since even higher contents of tetracene do not guarantee spontaneous ignition safety.
本発明は他の点火薬混合剤、例えば摩擦剤にも
関連する。このような薬剤は鉛トリニトロレゾル
シナート、塩酸カリ又は硝酸鉛又は硝酸バリウ
ム、珪化カルシウム、三硫化アンチモン及び硝子
粉または石英粉を含有する。このような薬剤の場
合にも刺突敏感性を高めるために、爆燃温度を
200℃以下にすることなしに微細粒度のテトラセ
ンを2〜8%の割合で加えることができる。 The invention also relates to other ignition powder admixtures, such as friction agents. Such agents include lead trinitroresorcinates, potassium hydrochloride or lead or barium nitrate, calcium silicide, antimony trisulfide and glass or quartz powder. In order to increase the puncture sensitivity of such drugs, the deflagration temperature may also be increased.
Fine-grained tetracene can be added in proportions of 2 to 8% without lowering the temperature below 200°C.
総括的に点火薬混合剤に対する記述の諸実験か
ら次のような特性が判明する。 Overall, the following characteristics are revealed from the various experiments described for the ignition powder mixture.
(1) 爆燃温度は粒度に依存しており、粒度が大と
なるに伴つて爆燃温度は益々低くなり、爆燃温
度が200℃以下になる時最早自然発火安全性は
保証されない。(1) The deflagration temperature depends on the particle size, and as the particle size increases, the deflagration temperature becomes lower and lower, and when the deflagration temperature falls below 200℃, spontaneous ignition safety is no longer guaranteed.
(2) 刺突敏感性はテトラセンの割合に依存する。
テトラセンの割合が大となるにつれて刺突敏感
性は益々大となる。テトラセン含有量が過少な
場合には刺突敏感性は不十分である。(2) The puncture sensitivity depends on the proportion of tetracene.
As the proportion of tetracene increases, the puncture sensitivity becomes increasingly greater. If the tetracene content is too low, the puncture sensitivity is insufficient.
(3) 爆燃温度はテトラセンの割合にも依存する。
テトラセンの割合が大となるにつれて爆燃温度
は益々低くなり、かつ爆燃温度が200℃以下に
なる時最早自然発火安全性は保証されない。(3) Deflagration temperature also depends on the proportion of tetracene.
As the proportion of tetracene increases, the deflagration temperature becomes lower and lower, and when the deflagration temperature is below 200°C, spontaneous ignition safety is no longer guaranteed.
(4) 爆燃温度は雷管中の刺突点火薬の量に依存し
する。刺突点火薬混合剤の量が大となるにつれ
て爆燃温度は益々低くなり、200℃以下になる
時最早自然発火安全性は保証されない。(4) Deflagration temperature depends on the amount of piercing igniter in the detonator. As the amount of piercing igniter mixture increases, the deflagration temperature becomes lower and lower, and when it goes below 200°C, spontaneous ignition safety is no longer guaranteed.
(5) 刺突敏感性は同じく敏感点火剤のテトラセン
含有量に依存する。テトラセン含有量が小さく
なるにつれて、刺突敏感性は小さくなる。テト
ラセン含有量が過少な場合刺突敏感性は不十分
である。(5) Penetration sensitivity also depends on the tetracene content of the sensitive ignition agent. As the tetracene content decreases, the puncture sensitivity decreases. If the tetracene content is too low, the puncture sensitivity will be insufficient.
Claims (1)
トロペンタノン、トリメチレントリニトロアミ
ン、テトラメチレンテトラニトラミン、窒化鉛の
何れかの物質及びこれらから成る混合剤を含有す
る第2次爆薬を点火するために使用可能であり、
その場合2〜8重量%のテトラセンと98〜92重量
%の窒化鉛又は他の成分とを含有している刺突に
敏感な点火薬混合剤において、 200℃よりも高い爆燃温度に達するために、少
なくともテトラセンの大部分が10μmよりも大き
く40μmよりも小さい粒度を有することを特徴と
する刺突に敏感な点火薬混合剤。 2 他の成分が鉛トリニトロレゾルシナート、硝
酸バリウム、三硝化アンチモン及びカーボランダ
ムである、特許請求の範囲第1項記載の刺突に敏
感な点火薬混合剤。[Claims] 1. A secondary explosive containing any of the following substances: trinitrophenylmethylnitroamine, nitropentanone, trimethylenetrinitramine, tetramethylenetetranitramine, lead nitride, and a mixture thereof. can be used to ignite
In order to reach deflagration temperatures higher than 200 °C in puncture-sensitive igniter mixtures, then containing 2-8% by weight of tetracene and 98-92% by weight of lead nitride or other components. , a puncture-sensitive igniter mixture characterized in that at least the majority of the tetracene has a particle size greater than 10 μm and less than 40 μm. 2. The stab-sensitive igniter mixture according to claim 1, wherein the other components are lead trinitroresorcinate, barium nitrate, antimony trinitrate and carborundum.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH440477A CH594578A5 (en) | 1977-04-07 | 1977-04-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS53124605A JPS53124605A (en) | 1978-10-31 |
JPS6317798B2 true JPS6317798B2 (en) | 1988-04-15 |
Family
ID=4275499
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4044478A Granted JPS53124605A (en) | 1977-04-07 | 1978-04-07 | Ignition explosives blend agent being sensitive to piercive impact * production thereof and application to detonator |
Country Status (9)
Country | Link |
---|---|
JP (1) | JPS53124605A (en) |
BE (1) | BE865800A (en) |
CH (1) | CH594578A5 (en) |
DE (1) | DE2808394C3 (en) |
FR (1) | FR2386505A1 (en) |
GB (1) | GB1575170A (en) |
IT (1) | IT1093458B (en) |
NL (1) | NL172050C (en) |
SE (1) | SE426482B (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4608102A (en) * | 1984-11-14 | 1986-08-26 | Omark Industries, Inc. | Primer composition |
GB2313371B (en) * | 1990-04-04 | 1998-02-18 | Breed Automotive Tech | A high temperature stable,low input energy primer/detonator |
JP5458346B2 (en) * | 2008-07-16 | 2014-04-02 | 昭和金属工業株式会社 | Lead-free powder |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL3061C (en) * | ||||
DE265025C (en) * | 1912-12-08 | 1913-10-01 | Claessen Conrad | Process for the production of detonators for detonators, primers and projectile detonations |
DE362433C (en) * | 1921-03-06 | 1922-10-27 | Hans Rathsburg Dr | Process for the manufacture of ignition kits |
BE433547A (en) * | 1938-05-03 |
-
1977
- 1977-04-07 CH CH440477A patent/CH594578A5/xx not_active IP Right Cessation
- 1977-05-17 NL NLAANVRAGE7705471,A patent/NL172050C/en not_active IP Right Cessation
-
1978
- 1978-02-27 DE DE2808394A patent/DE2808394C3/en not_active Expired
- 1978-04-04 IT IT21947/78A patent/IT1093458B/en active
- 1978-04-04 GB GB13037/78A patent/GB1575170A/en not_active Expired
- 1978-04-04 SE SE7803767A patent/SE426482B/en not_active IP Right Cessation
- 1978-04-07 FR FR7810453A patent/FR2386505A1/en active Granted
- 1978-04-07 JP JP4044478A patent/JPS53124605A/en active Granted
- 1978-04-07 BE BE188648A patent/BE865800A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE2808394C3 (en) | 1980-04-24 |
NL172050B (en) | 1983-02-01 |
SE7803767L (en) | 1978-10-08 |
FR2386505B1 (en) | 1980-09-19 |
DE2808394A1 (en) | 1979-03-08 |
DE2808394B2 (en) | 1979-08-16 |
CH594578A5 (en) | 1978-01-13 |
SE426482B (en) | 1983-01-24 |
IT1093458B (en) | 1985-07-19 |
IT7821947A0 (en) | 1978-04-04 |
FR2386505A1 (en) | 1978-11-03 |
BE865800A (en) | 1978-07-31 |
JPS53124605A (en) | 1978-10-31 |
NL172050C (en) | 1983-07-01 |
NL7705471A (en) | 1978-10-10 |
GB1575170A (en) | 1980-09-17 |
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