JPS5815465B2 - Low or non-static ammonium nitrate explosive composition - Google Patents

Low or non-static ammonium nitrate explosive composition

Info

Publication number
JPS5815465B2
JPS5815465B2 JP2823380A JP2823380A JPS5815465B2 JP S5815465 B2 JPS5815465 B2 JP S5815465B2 JP 2823380 A JP2823380 A JP 2823380A JP 2823380 A JP2823380 A JP 2823380A JP S5815465 B2 JPS5815465 B2 JP S5815465B2
Authority
JP
Japan
Prior art keywords
oil
explosive composition
nitric
ammonium nitrate
static
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
Application number
JP2823380A
Other languages
Japanese (ja)
Other versions
JPS56125292A (en
Inventor
黒川孝一
酒井洋
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.)
NOF Corp
Original Assignee
Nippon Oil and Fats Co Ltd
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 Nippon Oil and Fats Co Ltd filed Critical Nippon Oil and Fats Co Ltd
Priority to JP2823380A priority Critical patent/JPS5815465B2/en
Publication of JPS56125292A publication Critical patent/JPS56125292A/en
Publication of JPS5815465B2 publication Critical patent/JPS5815465B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は特定の界面活性剤を含有する帯電性が非常に少
ない硝安油剤爆薬組成物又は非帯電性硝安油剤爆薬組成
物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an ammonium nitrate explosive composition containing a specific surfactant and having very little chargeability or a non-chargeable ammonium nitrate explosive composition.

硝安油剤爆薬(以下硝油爆薬と略記する)は、高感度の
鋭感剤を含まないことから製造上及び取扱上安全性が高
く、かつ安価であるため広く使用されている。
Ammonium nitrate explosives (hereinafter abbreviated as nitric oil explosives) are widely used because they do not contain highly sensitive sensitizing agents and are therefore safe in terms of manufacturing and handling, and are inexpensive.

一般に硝油爆薬は、圧縮空気を用いた装填機により被破
壊物の穿孔に装填されるが、その際硝油爆薬の粒子が装
填ホース及び穿孔中の高速度で送られるため、硝油爆薬
の粒子が装填ホース内壁面及び穿孔面に衝突し摩擦して
静電気が発生する。
Generally, nitrate explosives are loaded into holes in objects to be destroyed using a loading machine that uses compressed air. The particles collide with the inner wall surface of the loading hose and the perforated surface, causing friction and generating static electricity.

この静電気は、作業者、装填ホース、装填機および硝油
爆薬の粒子に帯電蓄積され、それらの電荷が一時に放電
すると電気雷管を爆発させる危険性があり、さらに人体
への電撃によって副次的な災害を起こす可能性もあって
静電気の帯電蓄積は保安上無視することのできない大き
な問題である。
This static electricity builds up on the operator, the loading hose, the loading machine, and the particles of the nitric oil explosive, and if those charges are discharged all at once, there is a danger of detonating the electric detonator, and there is also a secondary risk of electric shock to the human body. Accumulation of static electricity is a major safety issue that cannot be ignored, as it has the potential to cause serious disasters.

従来、静電気対策として金属製の容器や良導電体の装填
ホースを使用し、これらを完全に接地することが行われ
た。
Conventionally, as a countermeasure against static electricity, a metal container or a loading hose made of a good conductor was used, and these were completely grounded.

しかしこの対策は、発生した静電気が作業者、装填ホー
スおよび装填機に帯電蓄積することを防止しようとする
もので、硝油爆薬の粒子に帯電することに対しては何等
考慮されておらず、したがって穿孔に装填した硝油爆薬
に族ダイを装薬する際の暴発事故を絶滅することは困難
であった。
However, this countermeasure is intended to prevent the generated static electricity from accumulating on the operator, loading hose, and loading machine, but does not take into account the possibility that the particles of the nitric oil explosive will be charged. Therefore, it has been difficult to eliminate explosion accidents when the nitric oil explosives loaded into the borehole are charged with the group die.

硝油爆薬の粒子への帯電を少なくするために、爆薬10
0重量部に対して0.5〜4重量部の水を含有した硝油
爆薬組成物(特公昭43−9678号公報)が知られて
いる。
In order to reduce the charge on the particles of the nitric oil explosive, the explosive 10
A nitric oil explosive composition containing 0.5 to 4 parts by weight of water per 0 parts by weight (Japanese Patent Publication No. 43-9678) is known.

しかしながら、この硝油爆薬組成物は、硝酸アンモニウ
ム(以下硝安ど略記する)と水とが直接−触することに
よる爆発性能の低下を防止するために、水と燃料油とを
界面活性剤を用いて乳化しエマルジョンを形成しこれに
硝安を混合して製造されるものであって、エマルション
を形成させなければならないため製造が煩雑であり、か
つ非帯電性の程度も完全でなかった。
However, in order to prevent deterioration in explosive performance due to direct contact between ammonium nitrate (hereinafter abbreviated as ammonium nitrate) and water, this nitric oil explosive composition uses a surfactant to separate water and fuel oil. It is manufactured by emulsifying to form an emulsion and mixing ammonium nitrate with the emulsion, which is complicated to manufacture because the emulsion must be formed, and the degree of non-static property is not perfect.

又長期間保存しておくとエマルションが破壊し爆発性能
の低下の原因となっていた。
Furthermore, if stored for a long period of time, the emulsion would be destroyed, causing a decrease in explosive performance.

さらに水を含むことから爆発性能が低いという本質的な
問題があった。
Furthermore, there was the inherent problem that explosive performance was low because it contained water.

本発明の目的は、従来の硝油爆薬組成物の問題を解消し
て製造が容易で、経時安定性に優れ、非帯電性が格段に
優れた硝油爆薬組成物を提供することにある。
An object of the present invention is to solve the problems of conventional nitric oil explosive compositions and to provide a nitric oil explosive composition that is easy to manufacture, has excellent stability over time, and has extremely excellent non-static properties.

本発明者等は、燃料油に容易に溶解または分散し、かつ
硝安ど反応しない各種界面活性剤について鋭意研究した
結果、特定の界面活性剤を見い出し本発明を完成した。
As a result of extensive research into various surfactants that are easily dissolved or dispersed in fuel oil and do not react with nitric acid, the present inventors discovered a specific surfactant and completed the present invention.

本発明は、硝安ど燃料油とを主成分とする硝油爆薬組成
物に一般式 (式中のRは7〜10の炭素原子をもつアルキル基であ
り、mは2〜30である) で示されるポリオキシエチレンアルキルフェニルエーテ
ルを含有してなる帯電性の少ない又は非帯電性の硝油爆
薬組成物(以下、単に非帯電性硝油爆薬組成物と総称す
る)である。
The present invention provides a nitrate explosive composition containing nitric acid fuel oil as a main component, which has the general formula (in the formula, R is an alkyl group having 7 to 10 carbon atoms, and m is 2 to 30). This is a low or non-chargeable nitric oil explosive composition (hereinafter collectively referred to simply as a non-static nitric oil explosive composition) containing the polyoxyethylene alkylphenyl ether shown below.

本発明に用いられる硝安は、通常は粒状の硝安であるが
、特に従来から用いられている多孔性の粒状の硝安(プ
リル硝安)が爆発性能の向上の観点から好ましい。
The ammonium nitrate used in the present invention is usually granular ammonium nitrate, and the conventionally used porous granular ammonium nitrate (prilled ammonium nitrate) is particularly preferable from the viewpoint of improving explosive performance.

本発明に用いられる燃料油は、例えば、重油、軽油、灯
油、液状炭化水素等の石油系鉱油、鯨油、種油、コール
タールなどである。
Examples of the fuel oil used in the present invention include heavy oil, light oil, kerosene, petroleum mineral oil such as liquid hydrocarbon, whale oil, seed oil, and coal tar.

本発明において前記硝安および燃料油からなる主成分以
外に、例えば他の爆薬と区別するための顔料等の添加剤
が加えられてもよい。
In the present invention, in addition to the main components of ammonium nitrate and fuel oil, additives such as pigments may be added to distinguish the explosive from other explosives.

一本発明に用いられる特定の界面活性剤は、前記一般式
で示されるポリオキシエチレンアルキルフェニルエーテ
ルであるが、式中のアルキル基の炭素原子数が6以下又
は11以上の化合物でmが30より大きな数の化合物で
あると燃料油への溶解又は分散が十分でなく、さらに非
帯電性の効果が少ないために好ましくない。
A specific surfactant used in the present invention is a polyoxyethylene alkylphenyl ether represented by the above general formula, and is a compound in which the alkyl group in the formula has 6 or less carbon atoms or 11 or more carbon atoms, and m is 30 If the number of compounds is larger, the dissolution or dispersion in fuel oil will be insufficient, and the antistatic effect will be less, which is not preferable.

燃料油への溶解性又は分散性及び非帯電性の効果から、
特に好ましいポリオキシエチレンアルキルフェニルエー
テルは、前記一般式中のアルキル基の炭素原子数が9で
、mが6で示されるポリオキシエチレンノニルフェニル
エーテルである。
Due to its solubility or dispersibility in fuel oil and non-static effect,
A particularly preferred polyoxyethylene alkylphenyl ether is polyoxyethylene nonylphenyl ether in which the alkyl group in the general formula has 9 carbon atoms and m is 6.

又、本発明の非帯電性硝油爆薬組成物において、前記一
般式で示されるポリオキシエチレンアルキルフェニルエ
ーテルの含有量は、燃料油に対して通常約0.3〜15
%(重量基準、以下同様)であり、好ましくは0.5〜
10%である。
Further, in the non-chargeable nitric oil explosive composition of the present invention, the content of polyoxyethylene alkylphenyl ether represented by the above general formula is usually about 0.3 to 15% based on the fuel oil.
% (based on weight, the same applies hereinafter), preferably 0.5 to
It is 10%.

その含有量が0.3%未満であると非帯電性の効果が少
なく、又、15%を越えても非帯電性の効果は15%の
場合に比べて大巾な向上はみもれないので経済性の観点
から不利である。
If the content is less than 0.3%, the antistatic effect will be small, and even if it exceeds 15%, the antistatic effect will not be significantly improved compared to the case where the content is 15%. Therefore, it is disadvantageous from an economic point of view.

以上の成分からなる本発明の非帯電性硝油爆薬組成物は
、前記のポリオキシエチレンアルキルフェニルエーテル
を燃料油に溶解又は均一に分散し、次いでこれを硝安ど
混合することによって容易に製造することが出来る。
The non-chargeable nitric oil explosive composition of the present invention comprising the above components can be easily produced by dissolving or uniformly dispersing the polyoxyethylene alkyl phenyl ether in fuel oil and then mixing this with nitric acid. I can do it.

得られた非帯電性硝油爆薬組成物は、そのまま被破壊物
の穿孔内に装填して用いるか、又は適当な包装材に充填
して爆薬薬包とし、これを被破壊物の穿孔内に装填して
用いる。
The obtained non-charged nitric oil explosive composition can be used as it is by being loaded into the perforation of the object to be destroyed, or it can be filled into a suitable packaging material to form an explosive cartridge, which is then placed into the perforation of the object to be destroyed. Load and use.

前記のようにして得られた本発明の非帯電性硝油爆薬組
成物は、従来の水を含有する硝油爆薬組成物と比べ、前
記のポリオキシエチレンアルキルフェニルエーテルの作
用により格段に優れた非帯電性を示し、又本発明におい
ては水を含有していないため水を燃料油に乳化させてエ
マルションを形成させる工程が不要であり、かつ用いら
れる前記ポリオキシエチレンアルキルフェニルエーテル
が容易に燃料油に溶解又は分散するために製造が極めて
簡単であり、さらに用いられる前記ポリオキシエチレン
アルキルフェニルエーテルは硝安と反応してアンモニア
ガスを発生させることがなりので本発明の非帯電性硝油
爆薬組成物は爆発性能が高く、長期保存しておいても爆
発性能の低下がない等の特徴を有するものである。
The non-chargeable nitric oil explosive composition of the present invention obtained as described above is significantly superior to conventional nitric oil explosive compositions containing water due to the action of the polyoxyethylene alkylphenyl ether. Since the present invention does not contain water, there is no need for a step of emulsifying water into fuel oil to form an emulsion, and the polyoxyethylene alkyl phenyl ether used can easily be used as a fuel oil. The non-chargeable nitric oil explosive composition of the present invention is extremely easy to manufacture because it can be dissolved or dispersed in oil, and the polyoxyethylene alkyl phenyl ether used reacts with ammonium nitrate to generate ammonia gas. The material has characteristics such as high explosive performance and no deterioration in explosive performance even after long-term storage.

次に本発明の非帯電性硝油爆薬組成物を実施例および比
較例によって具体的に説明する。
Next, the non-chargeable nitric oil explosive composition of the present invention will be specifically explained with reference to Examples and Comparative Examples.

なお各例中の部数および%はすべて重量基準である。Note that all parts and percentages in each example are based on weight.

実施例 1 第1表に示すような配合組成の非帯電性硝油爆薬組成物
を下記のようにして製造した。
Example 1 A non-chargeable nitric oil explosive composition having the formulation shown in Table 1 was manufactured as follows.

まず60部の2号軽油にポリオキシエチレンアルキルフ
ェニルエーテル(日本油脂社製、ノニオンH3−204
,5)3部を溶解し、次いでそれに940部の通常のプ
リル硝安(住人化学工業社製)を加えて良く混合して非
帯電性硝油爆薬組成物を得た。
First, 60 parts of No. 2 diesel oil was added with polyoxyethylene alkyl phenyl ether (Nonion H3-204 manufactured by Nippon Oil & Fats Co., Ltd.).
, 5) was dissolved, and then 940 parts of ordinary prill ammonium nitrate (manufactured by Sumitomo Chemical Co., Ltd.) was added thereto and mixed well to obtain a non-chargeable nitric oil explosive composition.

この非帯電性硝油爆薬組成物500グを直径190mm
、長さ350mmのポリエチレン製の袋に入れ袋の両端
を閉塞して薬包となし帯電圧の測定に供した。
500 g of this non-charged nitric oil explosive composition was heated to a diameter of 190 mm.
The mixture was placed in a polyethylene bag having a length of 350 mm, both ends of which were closed, and the electrostatic potential of the bag was measured.

帯電圧の測定方法は、前記薬包を60回/分の速度で回
転させることにより静電気を発生させ、袋の外側の帯電
圧を静電電圧計(春日電機社製)で測定し摩擦回数と帯
電圧の関係曲線を求めその結果を第1図に曲線E−1と
して実線で示した。
The charging voltage is measured by rotating the drug bag at a speed of 60 times per minute to generate static electricity, measuring the charging voltage on the outside of the bag with an electrostatic voltmeter (manufactured by Kasuga Denki Co., Ltd.), and calculating the number of frictions and the charging voltage. A voltage relationship curve was determined and the results are shown in FIG. 1 as a solid line as curve E-1.

図中摩擦回数N(n)は横軸に、帯電圧E(Kv)は縦
軸に目盛った。
In the figure, the number of times of friction N(n) is scaled on the horizontal axis, and the charging voltage E (Kv) is scaled on the vertical axis.

なお測定中の室温は8〜10℃、湿度は40〜45%で
あった。
Note that the room temperature during the measurement was 8 to 10°C, and the humidity was 40 to 45%.

又、前記非帯電性硝油爆薬組成物190vを内径3
5gm、肉厚3mm1長さ250mmの鉄管に入れ、鉄
管内の硝油爆薬組成物の比重を0.85にした薬包を合
計2本製造した。
Further, the uncharged nitric oil explosive composition 190v was
A total of two medicine packets were manufactured by placing the powder into an iron tube of 5 gm, wall thickness of 3 mm, and length of 250 mm, with the specific gravity of the nitric oil explosive composition in the iron tube being 0.85.

2本のうち1本は直ちに爆速の測定に供し、残り1本は
2力月間保管した後爆速の測定に供した。
One of the two tubes was immediately used for detonation velocity measurement, and the remaining one was stored for two months before being used for detonation velocity measurement.

なお爆速の測定は通常のカウンター法により行なった。The explosion speed was measured using a conventional counter method.

ただし起爆薬包として2号榎ダイナマイト50グを使用
し、それぞれの測定結果は第1表に示した。
However, 50 grams of No. 2 Enoki dynamite was used as the explosive cartridge, and the measurement results are shown in Table 1.

実施例 2〜5 第1表に示すようにポリオキシエチレンアルキルフェニ
ルエーテルの種類を替えた以外は、実施例1に準じて非
帯電性硝油爆薬組成物を製造した。
Examples 2 to 5 Non-chargeable nitric oil explosive compositions were produced according to Example 1, except that the type of polyoxyethylene alkyl phenyl ether was changed as shown in Table 1.

これらの非帯電性硝油爆薬組成物を用いて実施例1と同
様な方法でそれぞれの薬包を得た。
Each cartridge was obtained in the same manner as in Example 1 using these non-chargeable nitric oil explosive compositions.

この薬包を用いて実施例1と同じ方法で帯電圧の測定を
行ない結果を第1図にそれぞれ、曲線E−2,E−3,
E−4およびE−5として実線で示した。
Using this medicine package, the charging voltage was measured in the same manner as in Example 1, and the results are shown in Figure 1, curves E-2, E-3, and E-3, respectively.
They are shown as solid lines as E-4 and E-5.

又、爆速の測定においても実施例1と同じ方法で測定し
結果をそれぞれ第1表に示した。
The detonation velocity was also measured using the same method as in Example 1, and the results are shown in Table 1.

実施例 6〜11 第1表に示すようにアルキル基の炭素数9のポリオキシ
エチレンノニルフェニルエーテルヲ用い、2号軽油に対
する添加量をそれぞれ替えた以外は、実施例1に準じて
非帯電性硝油爆薬組成物を製造した。
Examples 6 to 11 As shown in Table 1, polyoxyethylene nonylphenyl ether having an alkyl group of 9 carbon atoms was used, and the amount of addition to No. 2 diesel oil was changed, respectively, in the same manner as in Example 1. A nitric oil explosive composition was produced.

ただし実施例10は添加量を実施例1と同じとした。However, in Example 10, the amount added was the same as in Example 1.

これらの非帯電性硝油爆薬組成物を用いて実施例1と同
様な方法でそれぞれ薬包を得た。
Using these non-chargeable nitric oil explosive compositions, cartridges were obtained in the same manner as in Example 1.

この薬包を用いて実施例1と同じ方法で帯電圧の測定を
行ない結果を第1図にそれぞれ曲線E−6゜E−7,E
−8,E−9,E−10およびE−11として実線で示
した。
Using this medicine package, the electrostatic voltage was measured in the same manner as in Example 1, and the results are shown in Figure 1 as curves E-6, E-7, and E, respectively.
-8, E-9, E-10 and E-11 are shown as solid lines.

又、爆速の測定においても実施例1と同じ方法で測定し
結果をそれぞれ第1表に示した。
The detonation velocity was also measured using the same method as in Example 1, and the results are shown in Table 1.

比較例 1 第2表に示すようにポリオキシエチレンアルキルフェニ
ルエーテルを日本油脂社製のノニオンMS−240に替
えた以外は実施例1に準じて非帯電性硝油爆薬組成物を
製造した。
Comparative Example 1 As shown in Table 2, a non-chargeable nitric oil explosive composition was produced according to Example 1 except that the polyoxyethylene alkyl phenyl ether was replaced with Nonion MS-240 manufactured by NOF Corporation.

この非帯電性硝油爆薬組成物を用いて実施例1と同様な
方法で薬包を得た。
A medicine package was obtained in the same manner as in Example 1 using this non-chargeable nitric oil explosive composition.

この薬包を用いて実施例1と同じ方法で帯電圧の測定を
行ない結果を第1図に曲線C−1として破線で示した。
Using this medicine package, the charging voltage was measured in the same manner as in Example 1, and the results are shown in FIG. 1 by a broken line as curve C-1.

又爆速の測定においても実施例1と同じ方法で測定し結
果を第2表に示した。
The detonation velocity was also measured using the same method as in Example 1, and the results are shown in Table 2.

比較例 2 第2表に示すようなポリオキシエチレンアルキルフェニ
ルエーテルを含有しない配合組成の硝油爆薬組成物を下
記のようにして製造した。
Comparative Example 2 A nitric oil explosive composition containing no polyoxyethylene alkylphenyl ether as shown in Table 2 was produced as follows.

60部の2号軽油に940部の通常のプリル硝安(住人
化学工業社製)を加えて良く混合して硝油爆薬組成物を
得た。
940 parts of ordinary prill ammonium nitrate (manufactured by Sumima Kagaku Kogyo Co., Ltd.) was added to 60 parts of No. 2 diesel oil and mixed well to obtain a nitric oil explosive composition.

この硝油爆薬組成物を用いて実施例1と同様な方法で薬
包を得た。
A cartridge was obtained in the same manner as in Example 1 using this nitric oil explosive composition.

この薬包を用いて実施例1と同じ方法で帯電圧の測定を
行ない結果を第1図に曲線C−2として破線で示した。
Using this medicine package, the charging voltage was measured in the same manner as in Example 1, and the results are shown in FIG. 1 as curve C-2 by a broken line.

又爆速の測定においても実施例1と同じ方法で測定し結
果を第2表に示した。
The detonation velocity was also measured using the same method as in Example 1, and the results are shown in Table 2.

比較例 3 第2表に示すように水を含有した配合組成の硝油爆薬組
成物を下記のようにして製造した。
Comparative Example 3 A nitric oil explosive composition containing water as shown in Table 2 was manufactured as follows.

まず60部の2号軽油に40部の水を加え、次いで乳化
剤(日本油脂社製、ディスパノール86)1部を加えて
よ(攪拌してエマルションを得、さらにこれに通常のプ
リル硝安(住人化学工業社製)940部を加えてよ(混
合して硝油爆薬組成物を得た。
First, add 40 parts of water to 60 parts of No. 2 diesel oil, then add 1 part of an emulsifier (Dispanol 86, manufactured by Nippon Oil & Fats Co., Ltd.) (stir to obtain an emulsion, and then add ordinary prill ammonium nitrate (Niman) to this. (manufactured by Kagaku Kogyo Co., Ltd.) (mixed) to obtain a nitric oil explosive composition.

この硝油爆薬組成−を用いて実施例1と同様な方法で薬
包を得た。
A cartridge was obtained in the same manner as in Example 1 using this nitric oil explosive composition.

この薬包を用いて実施例1と同じ方法で帯電圧の測定を
行ない結果を第1図に曲線C−3として破線で示した。
Using this medicine package, the charging voltage was measured in the same manner as in Example 1, and the results are shown in FIG. 1 by a broken line as curve C-3.

又爆速の測定においても実施例1と同じ方法で測定し結
果を第2表に示した。
The detonation velocity was also measured using the same method as in Example 1, and the results are shown in Table 2.

いずれも日本油脂社製のもので、実施例1〜5は実施例
1から順にノニオンH8−204,5、ノニオンH8−
210、ノニオンH8−220、ノニオンH8−230
、ノニオンN5−zo4.5を、また実施例6〜11は
ノニオンNS−206を使用した。
All of them are manufactured by NOF Corporation, and Examples 1 to 5 are Nonion H8-204,5, Nonion H8-204,5 in order from Example 1.
210, Nonion H8-220, Nonion H8-230
, Nonion N5-zo4.5 was used, and Examples 6 to 11 used Nonion NS-206.

ポリオキシエチレンアルキルフェニルエーテルの添加量
はいずれも2号軽油に対する重量%で示した。
The amount of polyoxyethylene alkyl phenyl ether added is expressed in weight percent based on No. 2 light oil.

第1図において本発明の非帯電性硝油爆薬組成物の非帯
電性は曲線E−1〜E−11(実施例1〜11)から明
らかなように、何も対策のとられていない従来の硝油爆
薬組成物の非帯電性を示す曲線C−2(比較例2)と比
べ格段に優れた非帯電性を示し、又水を含有する従来の
硝油爆薬組成物の非帯電性を示す曲線C−3(比較例3
)と較べても優れた非帯電性を示している。
In FIG. 1, as is clear from curves E-1 to E-11 (Examples 1 to 11), the non-charging property of the non-charging nitric oil explosive composition of the present invention is It shows significantly superior non-static properties compared to curve C-2 (Comparative Example 2) showing the non-static properties of the nitric oil explosive composition of Curve C-3 (Comparative Example 3)
) shows excellent antistatic properties.

特にポリオキシエチレンノニルフェニルエーテルを用い
た実施例6〜11においては、その添加量を増加する程
、非帯電性は明らかに向上している。
Particularly in Examples 6 to 11 in which polyoxyethylene nonylphenyl ether was used, the antistatic property clearly improved as the amount added increased.

しかしオキシエチレン基の数(m)が40であるポリオ
キシエチレンオクチルフェニルエーテルを用いた硝油爆
薬組成物の非帯電性は曲線C−1(比較例1)で示され
る通り摩擦回数Nの増加に伴って向上するが約150回
で逆に減少する傾向を示している。
However, as shown by curve C-1 (Comparative Example 1), the non-static property of the nitrate oil explosive composition using polyoxyethylene octylphenyl ether in which the number (m) of oxyethylene groups is 40 increases as the number of frictions N increases. However, it shows a tendency to decrease after about 150 times.

又第1表において示される通り本発明の非帯電性硝油爆
薬組成物の爆速は、第2表に示される水を含有する従来
の硝油爆薬組成物(比較例3)の爆速に比べ明らかに犬
である。
Furthermore, as shown in Table 1, the detonation speed of the non-charged nitric oil explosive composition of the present invention is clearly compared to the detonation speed of the conventional nitric oil explosive composition containing water (Comparative Example 3) shown in Table 2. is a dog.

さらに第1表において示される通り本発明の非帯電性硝
油爆薬組成物の爆速における経時変化は、はとんどない
のに対し、第2表に示される水を含有する従来の硝油爆
薬組成物(比較例3)のそれは、爆速か低下する傾向を
示している。
Furthermore, as shown in Table 1, the detonation velocity of the non-charged nitric oil explosive composition of the present invention changes little with time, whereas that of the conventional nitric oil explosive composition containing water as shown in Table 2. The composition (Comparative Example 3) shows a tendency for the explosion speed to decrease.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は摩擦回数Nと帯電圧Eとの関係を示す特性図で
あり、実線は本発明の非帯電性硝安油剤爆薬組成物を用
いた時の特性を、破線は従来の硝安油剤爆薬組成物又は
本発明の範囲外の硝安油剤爆薬組成物をそれぞれ用いた
時の特性を示す。 図中、曲線と実施例又は比較例との関係は次のとおりで
ある。 E−1:実施例1、E−2:実施例2、E−3:実施例
3、E−4:実施例4、E−5:実施例5、E−6:実
施例6、E−7:実施例7、E−8:実施例8、E−9
:実施例9、E−10:実施例10、E−11:実施例
11、C−1:比較例1、C−2:比較例2、C−3:
比較例3゜
FIG. 1 is a characteristic diagram showing the relationship between the number of frictions N and the charging voltage E, where the solid line shows the characteristics when using the non-chargeable ammonium nitrate explosive composition of the present invention, and the broken line shows the characteristics when using the conventional ammonium nitrate explosive composition. 2 shows the characteristics when using an ammonium nitrate oil explosive composition or an ammonium nitrate oil explosive composition outside the scope of the present invention. In the figure, the relationship between the curve and the example or comparative example is as follows. E-1: Example 1, E-2: Example 2, E-3: Example 3, E-4: Example 4, E-5: Example 5, E-6: Example 6, E- 7: Example 7, E-8: Example 8, E-9
: Example 9, E-10: Example 10, E-11: Example 11, C-1: Comparative example 1, C-2: Comparative example 2, C-3:
Comparative example 3゜

Claims (1)

【特許請求の範囲】 1 硝酸アンモニウムと燃料油とを主成分とする硝安油
剤爆薬組成物において一般式 (式中のRは7〜10の炭素原子をもつアルキル基であ
り、mは2〜30である) で示されるポリオキシエチレンアルキルフェニルエーテ
ルを含有してなることを特徴とする帯電性の少ない又は
非帯電性の硝安油剤爆薬組成物。 2 ポリオキシエチレンアルキルフェニルエーテルが で示される化合物であり、その量が燃料油に対して0.
3〜15重量%である特許請求の範囲第1項に記載の帯
電性の少ない又は非帯電性の硝安油剤爆薬組成物。
[Scope of Claims] 1. In an ammonium nitrate explosive composition containing ammonium nitrate and fuel oil as main components, the general formula (wherein R is an alkyl group having 7 to 10 carbon atoms, m is 2 to 30, 1. An ammonium nitrate oil explosive composition with low or non-electrostatic properties, characterized by containing a polyoxyethylene alkyl phenyl ether represented by the following. 2 Polyoxyethylene alkyl phenyl ether is a compound represented by the following formula, and the amount thereof is 0.0% relative to fuel oil.
3 to 15% by weight of the ammonium nitrate explosive composition with low or non-static chargeability according to claim 1.
JP2823380A 1980-03-06 1980-03-06 Low or non-static ammonium nitrate explosive composition Expired JPS5815465B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2823380A JPS5815465B2 (en) 1980-03-06 1980-03-06 Low or non-static ammonium nitrate explosive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2823380A JPS5815465B2 (en) 1980-03-06 1980-03-06 Low or non-static ammonium nitrate explosive composition

Publications (2)

Publication Number Publication Date
JPS56125292A JPS56125292A (en) 1981-10-01
JPS5815465B2 true JPS5815465B2 (en) 1983-03-25

Family

ID=12242870

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2823380A Expired JPS5815465B2 (en) 1980-03-06 1980-03-06 Low or non-static ammonium nitrate explosive composition

Country Status (1)

Country Link
JP (1) JPS5815465B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5973487A (en) * 1982-10-19 1984-04-25 旭化成株式会社 Heat resistant ammonium nitrate explosive composition
JP2002224372A (en) * 2001-02-06 2002-08-13 Fuji Shoji:Kk Pachinko game machine

Also Published As

Publication number Publication date
JPS56125292A (en) 1981-10-01

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