EP0123008B1 - Zusammensetzungen vom "Emulsion explosiv" Typ, Verfahren zu ihrer Herstellung und Anwendung dieser Zusammensetzungen - Google Patents

Zusammensetzungen vom "Emulsion explosiv" Typ, Verfahren zu ihrer Herstellung und Anwendung dieser Zusammensetzungen Download PDF

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Publication number
EP0123008B1
EP0123008B1 EP83870026A EP83870026A EP0123008B1 EP 0123008 B1 EP0123008 B1 EP 0123008B1 EP 83870026 A EP83870026 A EP 83870026A EP 83870026 A EP83870026 A EP 83870026A EP 0123008 B1 EP0123008 B1 EP 0123008B1
Authority
EP
European Patent Office
Prior art keywords
inert
parts
composition according
explosive
premix
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
EP83870026A
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English (en)
French (fr)
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EP0123008A1 (de
Inventor
Jean-Claude Libouton
Lucien Waterlot
Georges Van Roy
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Prb Nobel Explosifs SA
Original Assignee
Prb Nobel Explosifs SA
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 Prb Nobel Explosifs SA filed Critical Prb Nobel Explosifs SA
Priority to EP83870026A priority Critical patent/EP0123008B1/de
Priority to DE8383870026T priority patent/DE3380302D1/de
Priority to AT83870026T priority patent/ATE45135T1/de
Priority to ZA838344A priority patent/ZA838344B/xx
Priority to US06/585,554 priority patent/US4566920A/en
Priority to JP59050148A priority patent/JPS59232988A/ja
Priority to AU25695/84A priority patent/AU563845B2/en
Publication of EP0123008A1 publication Critical patent/EP0123008A1/de
Application granted granted Critical
Publication of EP0123008B1 publication Critical patent/EP0123008B1/de
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B23/00Compositions characterised by non-explosive or non-thermic constituents
    • C06B23/001Fillers, gelling and thickening agents (e.g. fibres), absorbents for nitroglycerine
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B21/00Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
    • C06B21/0033Shaping the mixture
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B47/00Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
    • C06B47/14Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase comprising a solid component and an aqueous phase
    • C06B47/145Water in oil emulsion type explosives in which a carbonaceous fuel forms the continuous phase
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S149/00Explosive and thermic compositions or charges
    • Y10S149/11Particle size of a component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S149/00Explosive and thermic compositions or charges
    • Y10S149/11Particle size of a component
    • Y10S149/112Inorganic nitrogen-oxygen salt

Definitions

  • the present invention relates to explosive compositions of the water-in-oil emulsion type, their manufacturing process and their application.
  • Another means, of more recent origin, consists in producing a much more intimate mixture between the solution of oxidizing nitrates and the fuel oil by combining them in the form of an emulsion.
  • an aqueous solution of the oxidizer is emulsified in the form of a dispersed phase inside a continuous carbonaceous combustible phase; a lightening constituent introduced in the form of mechanically included air, either in the form of a gas obtained by chemical means, or also in the form of microbubbles either spherical of the "microballoon" type, or in any form such as perlites, polyurethane, polyvinylidene chloride or expanded polystyrene is necessary to adjust the density and ensure sensitization in diameters which can be greatly reduced (of the order of 30 mm and less).
  • Patents US-A-3,447,978.4,008 108.4 110 134.4138,281 and 4,141,767, EP-A-0,019,458, DE-A-235,005 and BE-A-881,116 and 880,736 describe genre of compositions; numerous patents specify the nature of the oxidizer (s) used, that of the combustible oily phase, as well as that of the emulsifiers and gaseous constituents used.
  • an explosive emulsion consists of approximately 93 to 97% of an emulsified gel (in which 5 to 15 parts of water enter, 70 to 80 parts of one or more salts oxidizing minerals, 3 to 6 parts of combustible oil and possibly wax and 1 to 2 parts of emulsifier), to which approximately 3 to 7% of lightening material is added.
  • Document EP-A-18 085 discloses an explosive composition of the water-in-oil emulsion type comprising an emulsified gel, an inert lightening component and NaCl in an amount of 25%.
  • the emulsified gel consists of a solution of NH 4 N0 3 in water, an oily phase and an emulsifier.
  • the present invention relates firstly to an explosive composition of the water-in-oil emulsion type, comprising at least one emulsified gel, consisting of an oxidizing solution obtained from at least one mineral salt dissolved in water and d '' a combustible phase containing at least one liquid hydrocarbon and an emulsifier, associated with a lightening constituent, inert or reactive and, optionally, with one or more oxidizing salts or metallic fuels and / or inert materials, characterized in that '' it contains from 4 to 55% of inert or semi-inert solid materials which are silicates or diatomaceous earths or a mixture of the two at a rate of 1 to 4 parts of the former and 0 to 7 parts of the latter, depending on the degree of plasticity that we want to obtain.
  • emulsified gel consisting of an oxidizing solution obtained from at least one mineral salt dissolved in water and d '' a combustible phase containing at least one liquid hydro
  • inert and "semi-inert” must be understood in their acceptance of the technique of explosives. Mixtures of emulsified gel with inert or semi-inert materials, in proportions ranging from 96/4 to 45/55, always constitute true explosives whose detonation is complete and normal for as much as they contain the usual lightening component for water-in-oil type emulsions regulating their density and sensitization.
  • the safety character is obtained by the fact that the intervention of inert or semi-inert materials within the emulsified and aerated gel is marked by a reduction in its detonation speed (the latter being able to be adjusted to values less than 2000 m / s), and its energy potential, which are just as many fundamental factors in regulating the safety of an explosive.
  • the compositions comprise additions of inert materials from the family of chlorides or alkaline bicarbonates up to 10 to 45%, which makes it possible to obtain sureties such as those defined above, the salts to be taken into consideration being, inter alia, NaCI or NaHC0 3 .
  • This inert material can in particular be, in the case where it is desired to ensure safety of the P5 type, NaCl, with a particle size 250 to 500 microns and preferably at a content of 10 to 45%.
  • the inert material can be a premix of NaCl with a particle size of 250 to 500 microns, of calcium silicate and of diatomaceous earth, with a preferential content of 17 to 45%, comprising 15 to 38 parts of NaCl, 1 to 4 parts of calcium silicate and 0 to 7 parts of diatomaceous earth, which ensures both PS type security and paper cartridge filling on a conventional machine.
  • a semi-inert material which is a premix of N0 3 Na or N0 3 K, of which 80 to 90% of the grains are between 53 and 125 microns, and of NH 4 CI of which 50% of the grains are larger than 200 microns, calcium silicate and diatomaceous earth, at a content advantageously between 25 and 43%, comprising 11 to 24 parts of N0 3 Na or NO 3 K, 7 to 15 parts of NH 4 CI, 1 to 2 parts of silicate and 4 to 5 parts of diatomaceous earth, ensuring both P5 type safety and cartridge filling on a conventional machine.
  • part of the inert materials is calcium silicate, preferably of the silene or Calflo types and the diatomaceous earth is of the hyflosupersel type.
  • the lightening agent must have an apparent density of less than 30 g / liter; the one that has given the best results so far is expanded polystyrene at 18 g / liter.
  • an additional supply of oxygen must be provided to the composition by adding one or more inorganic oxidants.
  • This oxidant can be an inorganic nitrate, preferably of high molecular weight, optionally combined with an inorganic perchlorate.
  • inert materials the content of which remains between the limits already defined (from 4 to 55%), they consist essentially of extinguishing salts (NaCI for example) and sand.
  • NaCI extinguishing salts
  • the base gel content can be limited to 25 - 30% of the final composition.
  • the emulsion containing the lightening agent could be made extrudable on the cutting machine, without enjoying any kind of safety in the presence of an explosive gas atmosphere.
  • inert materials in the case where 10% of inert materials are used, it will be a premix comprising 2.5 to 3% of calcium silicate and 7.5 to 7% of diatomaceous earth; in the case where it is desired to use for example 45% of inert materials, it will be a premix consisting of 2.5 to 6% of silicate, 7.5 to 14% of diatomaceous earth and 25 to 35% of sand.
  • the diatomaceous earths could be replaced by hydrophobic, non-inert materials, such as calcium stearate; for this purpose, it is preferable to combine 1 to 3 parts of the latter with 3 to 7 parts of silicate; unlike the other additive materials taken into account until now, it is necessary to take into account in the calculation of the thermodynamic balance of the explosive of the fact that the stearates have an energy potential which takes part in the primary reaction of detonation.
  • Inert or semi-inert materials used both for extrusion and for safety in an explosive atmosphere, are, in the form of a premix, fed by means of a metering device into a continuous or discontinuous mixer, or they meet either the gel hot leaving the foaming device and the lightening component (continuous process) or a cold gel having already undergone a certain storage to which is also added the lightening component.
  • the finished product is poured or pumped onto the conveyor belt of the cartoning machine; if a hot gel is used, this strip must be cooled so that the temperature does not exceed approximately 40 ° C at the time of cutting.
  • the invention extends to the application of the explosive compositions of the invention having either a safety character with respect to the atmospheres encountered in coal mines, or the ability to be paper cartridges on a machine of the type classic, that is to say these two properties at the same time, while preserving with the explosive, even in small diameter of the normal characteristics of detonation.
  • the gel prepared at 75 ° C consists of:
  • 50% of the emulsified gel (hot or cooled) is mixed with 45% NaCl and 5% microbeads of type C15 - 250; NaCI is of a type whose particle size is between 250 and 500 microns.
  • Its safety is of the P5 type, it is not intended for extrusion on a Rollex machine, but it can be carted in plastic sheath on a Chub-Pack machine.
  • Example 1 50% of the emulsified gel of Example 1 is mixed with 45% of a premix consisting of 38 parts of NaCl and 7 parts of guhr and with 5% of Microbeads C15 - 250.
  • the explosive emulsion is such that it has both the safety characteristics of a P5 type explosive and the property of being paper-insertable on the cutting machine; in 30 mm, the density is 1.15 and the speed at detonator No. 8 is 2870 m / s for the fresh explosive; after 3 months, the speed is 2700 m / s.
  • the critical diameter of such a composition is between 10 and 15 mm; in diameter 15 mm, the speed is 2300 m / s. In ballistic mortar, the relative power is 20.8% of that of blasting gelatin.
  • the characteristics of the explosive emulsion of Example 2 do not change, but the extrudability is even better if the 7% of guhr is replaced by a mixture comprising 2% of calcium silicate, of type Silene or Calflo and 5% of diatomaceous earth of the Hyflosupersel type.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Colloid Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Cosmetics (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Claims (11)

1. Explosive Mischung vom Typ Wasser/Öl-Emulsion, mit mindestens einem emulgierten Gel aus einer oxydierenden Lösung, die aus mindestens einem in Wasser aufgelösten Salz und einer brennbaren Phase mit mindestens einem flüssigen Kohlenwasserstoff und einem Emulgator erhalten wurde, sowie mit einem inerten oder reaktiven Auflockerungsbestandteil und eventuell mit einen oder mehreren oxydierenden Salzen oder metallischen Brennstoffen, und/oder mit inerten Stoffen, dadurch gekennzeichnet, daß sie 4 bis 55 % inerte oder halbinerte Feststoffe enthält, aus Silikaten oder Diatomeenerden, oder aus einem Gemisch der beiden, mit 1 bis 4 Teilen Silikate und 0 bis 7 Teilen Diatomeenerden, je nach dem gewünschten Konsistenzgrad.
2. Mischung gemäß Anspruch 1, dadurch gekennzeichnet, daß das Silikat Calciumsilikat ist.
3. Mischung gemäß Anspruch 1 oder 2, dadurch gekennzeichnet, daß die Silikate und Diatomeenerden 4 bis 15 % der Mischung ausmachen.
4. Mischung gemäß irgendeinem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß sie Zusätze aus inerten Stoffen aus der Gruppe der Chloride oder der alkalischen Bikarbonate, vorzugsweise NaCl oder NaHC03, und zwar 10 bis 45 %, enthält, um Sicherheitssprengstoffe für die Steinkohlengruben zu erhalten.
5. Mischung gemäß Anspruch 4, dadurch gekennzeichnet, daß das besagte Salz NaCI mit einer Körnung von 250 bis 500 Mikron ist.
6. Mischung gemäß Anspruch 4, dadurch gekennzeichnet, daß mit dem Ziel der Sicherheit Salzkombinationen aus N03Na/NH4CI oder KN03/NH4Cl in nahe bei der stöchiometrischen Zusammensetzung liegenden Proportionen von 10 bis 45 % verwendet werden.
7. Mischung gemäß Anspruch 1, dadurch gekennzeichnet, daß der inerte Stoff aus einem Vorgemisch aus NaCl mit einer Körnung von 250 bis 500 Mikron, sowie Calciumsilikat, und Diatomeenerden mit einem bevorzugten Gehalt von 17 bis 45 % besteht, wobei dieses Vorgemisch 15 bis 38 Teile NaCI, 1 bis 4 Teile CalciumsilIkat und 0 bis 7 Teile Diatomeenerden enthält.
8. Mischung gemäß Anspruch 1, dadurch gekennzeichnet, daß ein halbinerter Stoff verwendet wird aus einem Vorgemisch aus N03Na oder N03K, bei dem 80 bis 90 % der Körner zwischen 53 und 125 Mikron liegen, und aus NH4CI, bei dem 50 % der Körner größer als 200 Mikron sind, sowie aus Calciumsilikat, und Diatomeenerden mit einem Gehalt, der vorzugsweise zwischen 25 und 43 % liegt, wobei dieses Vorgemisch 11 bis 24 Teile N03Na oder N03K, 7 bis 15 Teile NH4CI, 1 bis 2 Teile Silikat und 4 bis 5 Teile Diatomeenerden enthält.
9. Verfahren zum Herstellen von Mischungen gemäß irgendeinem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß die inerten oder halbinerten Stoffe in Form eines Vorgemischs mittels einer Dosiervorrichtung in einen kontinuierlichen oder diskontinuierlichen Mischer eingebracht werden, wo sie entweder mit dem aus dem Emulgator komnenden heißen Gel, dem Auflockerungsbestandteil, sowie den eventuellen Brennstoffen, oder mit einem kalten Gel, das bereits eine gewisse Zeit gelagert wurde, zusammentreffen, wobei zu diesem kalten Gel ebenfalls der Auflockerungsbestandteil und die eventuellen metallischen Brennstoffe hinzugegeben werden.
10. Verfahren gemäß Anspruch 9, dadurch gekennzeichnet, daß das Endprodukt auf das Förderband der Patronenfüllmaschine gegossen oder gepumpt wird, wobei dieses Förderband im Falle der Verwendung eines heißen Gels so abgekühlt wird, daß die Temperatur beim Einfüllen in die Patronen nicht höher als 40° C ist.
11. Anwendung der Mischungen gemäß irgendeinem der Ansprüche 1 bis 8 für Sprengstoffe, die entweder eine besondere Sicherheit gegenüber den gefährlichen Atmosphären in den Steinkohlengruben, oder die Möglichkeit des Einfüllens mit einer herkömmlichen Maschine (Schneide-, Schnecken- oder Ladestockmaschine) bieten, oder die diese zwei Eigenschaften gleichzeitig aufweisen, während bei dem Sprengstoff, und zwar selbst bei kleinen Durchmessern, normale Detonationseigenschaften erhalten bleiben.
EP83870026A 1983-03-18 1983-03-18 Zusammensetzungen vom "Emulsion explosiv" Typ, Verfahren zu ihrer Herstellung und Anwendung dieser Zusammensetzungen Expired EP0123008B1 (de)

Priority Applications (7)

Application Number Priority Date Filing Date Title
EP83870026A EP0123008B1 (de) 1983-03-18 1983-03-18 Zusammensetzungen vom "Emulsion explosiv" Typ, Verfahren zu ihrer Herstellung und Anwendung dieser Zusammensetzungen
DE8383870026T DE3380302D1 (en) 1983-03-18 1983-03-18 Compositions of the "emulsion explosive" type, process for their manufacture and use of these compositions
AT83870026T ATE45135T1 (de) 1983-03-18 1983-03-18 Zusammensetzungen vom ''emulsion explosiv'' typ, verfahren zu ihrer herstellung und anwendung dieser zusammensetzungen.
ZA838344A ZA838344B (en) 1983-03-18 1983-11-09 Compositions of the"explosive emulsion"type,process for their manufacture and application of these compositions
US06/585,554 US4566920A (en) 1983-03-18 1984-03-02 Compositions of the explosive emulsion type, process for their manufacture and application of these compositions
JP59050148A JPS59232988A (ja) 1983-03-18 1984-03-14 エマルジヨン型爆発性組成物とその製法
AU25695/84A AU563845B2 (en) 1983-03-18 1984-03-16 Water-in-oil emulsion explosive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP83870026A EP0123008B1 (de) 1983-03-18 1983-03-18 Zusammensetzungen vom "Emulsion explosiv" Typ, Verfahren zu ihrer Herstellung und Anwendung dieser Zusammensetzungen

Publications (2)

Publication Number Publication Date
EP0123008A1 EP0123008A1 (de) 1984-10-31
EP0123008B1 true EP0123008B1 (de) 1989-08-02

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EP83870026A Expired EP0123008B1 (de) 1983-03-18 1983-03-18 Zusammensetzungen vom "Emulsion explosiv" Typ, Verfahren zu ihrer Herstellung und Anwendung dieser Zusammensetzungen

Country Status (7)

Country Link
US (1) US4566920A (de)
EP (1) EP0123008B1 (de)
JP (1) JPS59232988A (de)
AT (1) ATE45135T1 (de)
AU (1) AU563845B2 (de)
DE (1) DE3380302D1 (de)
ZA (1) ZA838344B (de)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
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JPS6090888A (ja) * 1983-10-21 1985-05-22 日本油脂株式会社 油中水型エマルシヨン爆薬の製造方法
CA1259492A (en) * 1985-10-15 1989-09-19 Lawrence A. Cescon Emulsion-containing explosive compositions
EP0238210A3 (en) * 1986-03-14 1989-05-24 Imperial Chemical Industries Plc Solid explosive composition
US4678524A (en) * 1986-06-18 1987-07-07 Ireco Incorporated Cast explosive composition and method
DE3712488C1 (en) * 1987-04-13 1988-05-05 Dynamit Nobel Ag Use of silicone oils in water-in-oil emulsion explosives, and silicone oil-containing water-in-oil emulsion explosives having reduced surface tackiness
MW1888A1 (en) * 1987-06-29 1989-03-08 Aeci Ltd Explosive
SE8800593L (sv) * 1988-02-22 1989-08-23 Nitro Nobel Ab Spraengaemneskomposition
US5271779A (en) * 1988-02-22 1993-12-21 Nitro Nobel Ab Making a reduced volume strength blasting composition
US4867920A (en) * 1988-10-14 1989-09-19 Ireco Incorporated Emulsion explosive manufacturing method
GB8907992D0 (en) * 1989-04-10 1989-05-24 Ici Plc Emulsion explosive
US6554927B1 (en) * 2000-11-24 2003-04-29 Sigmabond Technologies Corporation Method of explosive bonding, composition therefor and product thereof
RU2565637C1 (ru) * 2014-06-10 2015-10-20 Федеральное казенное предприятие "Государственный научно-исследовательский институт химических продуктов" (ФКП "ГосНИИХП") Метательный заряд для 9 х 19 мм пистолетного патрона с облегченной пулей со стальным сердечником
CN110655431B (zh) * 2019-10-14 2023-11-10 山西北化关铝化工有限公司 一种瓦斯条件下专用射孔弹用主装药及其制备方法和应用
CN113582792A (zh) * 2021-08-20 2021-11-02 北京理工大学 一种发泡型富氟氧化剂基工业炸药及其制备方法

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GB1315197A (en) * 1970-07-13 1973-04-26 Explosives & Chem Prod Explosive gel compositions
DE2350605C3 (de) * 1973-10-09 1979-02-08 Idl Chemicals, Hyderabad (Indien) Verfahren zur Herstellung eines kapselempfindlichen, gelartigen Wettersprengstoffes
AU515896B2 (en) * 1976-11-09 1981-05-07 Atlas Powder Company Water-in-oil explosive
US4141767A (en) * 1978-03-03 1979-02-27 Ireco Chemicals Emulsion blasting agent
NZ192888A (en) * 1979-04-02 1982-03-30 Canadian Ind Water-in-oil microemulsion explosive compositions
US4231821A (en) * 1979-05-21 1980-11-04 Ireco Chemicals Emulsion blasting agent sensitized with perlite
US4294633A (en) * 1979-06-07 1981-10-13 Clay Robert B Blasting composition
US4394198A (en) * 1980-08-25 1983-07-19 Nippon Oil And Fats Company, Limited Water-in-oil emulsion explosive composition
US4364782A (en) * 1980-09-12 1982-12-21 Ireco Chemicals Permissible slurry explosive
US4371408A (en) * 1980-10-27 1983-02-01 Atlas Powder Company Low water emulsion explosive compositions optionally containing inert salts
JPS57117306A (en) * 1981-01-12 1982-07-21 Nippon Oil & Fats Co Ltd Water-in-oil emulsion type explosive composition
US4414044A (en) * 1981-05-11 1983-11-08 Nippon Oil And Fats, Co., Ltd. Water-in-oil emulsion explosive composition
GB2086363B (en) * 1981-10-12 1984-03-07 Atlas Powder Co Emulsion explosives containing a reduced amount of water
JPS59207889A (ja) * 1983-05-10 1984-11-26 日本油脂株式会社 油中水型エマルシヨン爆薬組成物

Also Published As

Publication number Publication date
JPS59232988A (ja) 1984-12-27
ATE45135T1 (de) 1989-08-15
AU563845B2 (en) 1987-07-23
AU2569584A (en) 1984-09-20
DE3380302D1 (en) 1989-09-07
ZA838344B (en) 1984-07-25
EP0123008A1 (de) 1984-10-31
US4566920A (en) 1986-01-28

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