JPH04114990A - Plastic explosive composed of polyurethane and nitramine - Google Patents

Plastic explosive composed of polyurethane and nitramine

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Publication number
JPH04114990A
JPH04114990A JP23034690A JP23034690A JPH04114990A JP H04114990 A JPH04114990 A JP H04114990A JP 23034690 A JP23034690 A JP 23034690A JP 23034690 A JP23034690 A JP 23034690A JP H04114990 A JPH04114990 A JP H04114990A
Authority
JP
Japan
Prior art keywords
nitramine
explosive
polyurethane
pts
alkyl
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.)
Pending
Application number
JP23034690A
Other languages
Japanese (ja)
Inventor
Shiyuuji Hodono
程野 修二
Shoji Nakahara
中原 正二
Miki Shibuya
渋谷 幹
Yukari Yonemura
米村 ゆかり
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chugoku Kayaku KK
Original Assignee
Chugoku Kayaku KK
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Chugoku Kayaku KK filed Critical Chugoku Kayaku KK
Priority to JP23034690A priority Critical patent/JPH04114990A/en
Publication of JPH04114990A publication Critical patent/JPH04114990A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To keep the plasticity of an explosive even at increased content of explosive without lowering the safety and detonation velocity by adding a specific resin additive to a main agent composed of a polyurethane resin and a nitramine explosive. CONSTITUTION:The objective explosive is produced by compounding (A) 100 pts.wt. of a main agent composed of 10 pts.wt. of a polyurethane resin component and 90 pts.wt. of a nitramine explosive component (e.g. tetramethylene tetranitramine) with (B) 0.01-3 pts.wt. of a resin additive selected from an alkyl or alkylallyl ether of polyoxyethylene, polyoxyethylene bisphenol A fatty acid ester and benzene di- and tricarboxylic acid alkyl ester.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、ポリウレタン樹脂とニトラミン系爆薬を主剤
とする可塑性爆薬(以下PBXという)に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a plastic explosive (hereinafter referred to as PBX) whose main ingredients are a polyurethane resin and a nitramine explosive.

従来技術 ニトラミン系爆薬は高性能で低感度のため従来のトリニ
トロトルエン(以下TNTという)系爆薬に置き変わり
つ−あるが、融点が高く、TNTのように弾体に溶融充
填することができない。TNTと融合し、溶融充填する
ことは可能であるが、TNTの配合比を多くする必要が
あり、爆薬の威力が低下する。また被弾により爆発する
という欠点もある。
Prior Art Nitramine-based explosives are replacing conventional trinitrotoluene (hereinafter referred to as TNT)-based explosives because of their high performance and low sensitivity, but they have a high melting point and cannot be melted and filled into bullets like TNT. Although it is possible to fuse with TNT and melt-fill it, it is necessary to increase the blending ratio of TNT, which reduces the power of the explosive. It also has the disadvantage of exploding when hit by a bullet.

弾体への爆薬の充填に際しては、気泡がないように充填
することが発射時仁高加速度を受ける砲弾ではとくに必
要であり、その方法としては溶融充填のほかに爆薬粉末
を樹脂と混合してPBXとして充填する方法がある。後
者の場合、爆発威力を増大させるためには爆薬成分の配
合比を多くすることが望まれるが、爆薬成分の配合比を
多くすると、可塑性が失われて粉状となる。
When filling explosives into a shell, it is especially necessary to fill the shell without air bubbles, especially for shells that are subject to high acceleration during firing. There is a way to fill it as a PBX. In the latter case, it is desirable to increase the blending ratio of explosive components in order to increase the explosive power, but if the blending ratio of explosive components is increased, plasticity is lost and the product becomes powdery.

発明が解決しようとする課題 本発明は、爆薬成分が高配合比でも可塑性を維持するこ
とができるポリウレタン・ニトラミン系PBXを提供す
ることを目的とする。
Problems to be Solved by the Invention An object of the present invention is to provide a polyurethane-nitramine-based PBX that can maintain plasticity even at a high blending ratio of explosive components.

課題の解決手段 本発明のポリウレタン・ニトラミン系PBXは、ポリウ
レタン樹脂とニトラミン系爆薬とを主剤とし、これに樹
脂添加剤(以下添加剤という)を(主剤100重量部に
対し好ましくは0.01〜3重量部、とくに好ましくは
0.25〜2重量部)添加したことを特徴とするもので
ある。
Means for Solving the Problems The polyurethane/nitramine-based PBX of the present invention has a polyurethane resin and a nitramine-based explosive as main ingredients, and a resin additive (hereinafter referred to as additive) (preferably 0.01 to 100 parts by weight per 100 parts by weight of the main agent). 3 parts by weight, particularly preferably 0.25 to 2 parts by weight).

本発明において使用される添加剤には次のようなものが
例示される。
Examples of additives used in the present invention include the following.

(1)ポリオキシエチレンのアルキルまたはアルキルア
リルエーテル RO(CHI CH20)nHRはアルキルまたはアル
キルアリル (2)ポリオキシエチレン ビスフェノールA 脂肪酸
エステル CH3 CHり −O(CHz GHz 0)ncORRはアルキル(3
)ベンゼンジカルボン酸のアルキルエステルCOOR−
C> G OOR Rはアルキル (4)ベンゼントリカルボン酸のアルキルエステルRO
OC−ζ)”C:::    、Rはアルキルこれら添
加剤は、常温で固体のものを使用することもできるが、
好ましくは液体のものが使用される。また上記添加剤は
単独で使用してもよいし、混合物として使用してもよい
(1) Alkyl or alkyl allyl ether of polyoxyethylene RO (CHI CH20) nHR is alkyl or alkylaryl (2) Polyoxyethylene bisphenol A fatty acid ester CH3 CH -O (CHz GHz 0) ncORR is alkyl (3
) Alkyl ester of benzenedicarboxylic acid COOR-
C> G OOR R is alkyl (4) benzenetricarboxylic acid alkyl ester RO
OC-ζ)"C::: , R is alkyl These additives can be solid at room temperature, but
Preferably liquids are used. Further, the above additives may be used alone or as a mixture.

ニトラミン系爆薬としては、テトラメチレンテトラニト
ラミン(以下HMXという)、トリメチレントリニトラ
ミン(以下RDXという)が代表的な例として挙げられ
る。
Typical examples of nitramine-based explosives include tetramethylenetetranitramine (hereinafter referred to as HMX) and trimethylenetrinitramine (hereinafter referred to as RDX).

実施例 第1表のNO61〜N0.7は本発明に係るPBXの組
成例を示すもので、ポリウレタン樹脂成分は、2.4−
)ルエン ジイソシアネート 0.48部、ポリエチレ
ングリコール(平均分子1114000) 1.80部
、1.1.1−トリス(ヒドロキシメチル)プロパン0
゜18部、ビス(2,2−ジニトロプロピル)アセター
ル−ビス(2,2−ジニトロプロピル)ホルマール重量
比1:1混合物 7.43部、フェニール−βナフチル
アミン0.10部、及び鉄(■価)アセチルアセトネー
ト 0.01部からなる。
Examples No. 61 to No. 0.7 in Table 1 indicate composition examples of PBX according to the present invention, and the polyurethane resin component is 2.4-
) Luene diisocyanate 0.48 parts, polyethylene glycol (average molecular weight 1114000) 1.80 parts, 1.1.1-tris(hydroxymethyl)propane 0
18 parts of bis(2,2-dinitropropyl) acetal-bis(2,2-dinitropropyl) formal in a weight ratio of 1:1, 7.43 parts of phenyl-β-naphthylamine, and 0.10 parts of phenyl-β-naphthylamine. ) 0.01 part of acetylacetonate.

爆薬成分はHMXまたはRDX90部である。The explosive component is 90 parts HMX or RDX.

添加物の添加量は0.25〜2.0重量部である。The amount of additives added is 0.25 to 2.0 parts by weight.

以上に示す原料のうち、2.4−トルエン ジイソシア
ネートを除く成分について、温度65℃、圧カフmm水
銀で30分間攪拌し、更に2.4−)ルエンジイソシア
ネートを加えて、65℃、7n水銀で30分間攪拌した
のち60℃で72時間硬化させた。
Among the raw materials shown above, the components except 2.4-toluene diisocyanate were stirred at a temperature of 65°C with a pressure cuff of mm mercury for 30 minutes, then 2.4-) toluene diisocyanate was added, and the mixture was stirred with 7n mercury at 65°C. After stirring for 30 minutes, the mixture was cured at 60° C. for 72 hours.

以上のようにして得たPBXと、添加物を添加しないN
018及びN009に示す比較例のPBXについて、常
法により引張り試験を行った。第2表に最大引張り強度
と伸びを示す。
PBX obtained as above and N without additives
A tensile test was conducted on the PBX of Comparative Examples shown in No. 018 and No. 009 using a conventional method. Table 2 shows the maximum tensile strength and elongation.

比較例のNo、8及びNO,9については共にテストピ
ース作製用のテストピースを取出した際、ぼろぼろに崩
れて試験することができなかった。
Regarding Comparative Examples No. 8 and No. 9, when the test pieces for test piece production were taken out, they fell apart and could not be tested.

同表から見られるように、添加物の添加効果は明瞭であ
る。
As seen from the table, the effect of adding additives is clear.

実施例で使用した添加物は、常温で液状またはろう状で
あり、添加量も少ないので比較例と比べて感度及び爆速
か余り変わらないことは容易に予測できるが、その例を
挙げると第3表に示すようになる。
The additives used in the examples are liquid or waxy at room temperature, and the amount added is small, so it is easy to predict that the sensitivity and explosion speed will not be much different compared to the comparative examples. The result will be as shown in the table.

同表から見られるように、添加物の添加により感度及び
爆速か損なわれることはなく、感度は若干鈍感になり、
爆速は若干向上した。
As can be seen from the table, the addition of additives does not impair the sensitivity or explosion speed, but the sensitivity becomes slightly insensitive.
Explosive speed has improved slightly.

発明の効果 本発明のポリウレタン・ニトラミン系PBXによれば以
上のように、添加物を配合することによりニトラミン系
爆薬の配合割合が多くても安全性及び爆速を損なわずに
PBXの可塑性を維持することができる。
Effects of the Invention According to the polyurethane-nitramine-based PBX of the present invention, as described above, by incorporating additives, the plasticity of the PBX can be maintained without impairing safety and detonation speed even if the blending ratio of nitramine-based explosive is high. be able to.

Claims (5)

【特許請求の範囲】[Claims] (1)ポリウレタン樹脂とニトラミン系爆薬とを主剤と
し、これに樹脂添加剤を添加したことを特徴とするポリ
ウレタン・ニトラミン系可塑性爆薬。
(1) A polyurethane/nitramine plastic explosive characterized by having a polyurethane resin and a nitramine explosive as main ingredients, to which a resin additive is added.
(2)樹脂添加剤は主剤100重量部に対し0.01〜
3重量部添加される請求項1記載のポリウレタン・ニト
ラミン系可塑性爆薬。
(2) The resin additive is 0.01 to 100 parts by weight of the main resin.
The polyurethane-nitramine plastic explosive according to claim 1, which is added in an amount of 3 parts by weight.
(3)樹脂添加剤はポリオキシエチレンのアルキルまた
はアルキルアリルエーテルである請求項1記載のポリウ
レタン・ニトラミン系可塑性爆薬。
(3) The polyurethane/nitramine plastic explosive according to claim 1, wherein the resin additive is an alkyl or alkyl allyl ether of polyoxyethylene.
(4)樹脂添加剤はポリオキシエチレンビスフェノール
A脂肪酸エステルである請求項1記載のポリウレタン・
ニトラミン系可塑性爆薬。
(4) The polyurethane according to claim 1, wherein the resin additive is polyoxyethylene bisphenol A fatty acid ester.
Nitramine plastic explosive.
(5)樹脂添加剤はベンゼンジ及びトリカルボン酸のア
ルキルエステルである請求項1記載のポリウレタン・ニ
トラミン系可塑性爆薬。
(5) The polyurethane-nitramine plastic explosive according to claim 1, wherein the resin additive is an alkyl ester of benzenedi and tricarboxylic acid.
JP23034690A 1990-08-30 1990-08-30 Plastic explosive composed of polyurethane and nitramine Pending JPH04114990A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23034690A JPH04114990A (en) 1990-08-30 1990-08-30 Plastic explosive composed of polyurethane and nitramine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23034690A JPH04114990A (en) 1990-08-30 1990-08-30 Plastic explosive composed of polyurethane and nitramine

Publications (1)

Publication Number Publication Date
JPH04114990A true JPH04114990A (en) 1992-04-15

Family

ID=16906412

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23034690A Pending JPH04114990A (en) 1990-08-30 1990-08-30 Plastic explosive composed of polyurethane and nitramine

Country Status (1)

Country Link
JP (1) JPH04114990A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009062394A (en) * 1999-06-18 2009-03-26 Basf Se Cyclohexane-1,4-dicarboxylic acid di(2-ethylhexyl)ester, method of producing the same, and plasticizer containig cyclohexane-1,4-dicarboxylic acid di(2-ethylhexyl)ester
US20110168306A1 (en) * 2008-08-29 2011-07-14 Bae Systems Plc Cast explosive composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009062394A (en) * 1999-06-18 2009-03-26 Basf Se Cyclohexane-1,4-dicarboxylic acid di(2-ethylhexyl)ester, method of producing the same, and plasticizer containig cyclohexane-1,4-dicarboxylic acid di(2-ethylhexyl)ester
US20110168306A1 (en) * 2008-08-29 2011-07-14 Bae Systems Plc Cast explosive composition
JP2015145329A (en) * 2008-08-29 2015-08-13 ビ−エイイ− システムズ パブリック リミテッド カンパニ−BAE SYSTEMS plc Casting explosive composition

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