WO2003053884A1 - Explosif - Google Patents
Explosif Download PDFInfo
- Publication number
- WO2003053884A1 WO2003053884A1 PCT/JP2002/013222 JP0213222W WO03053884A1 WO 2003053884 A1 WO2003053884 A1 WO 2003053884A1 JP 0213222 W JP0213222 W JP 0213222W WO 03053884 A1 WO03053884 A1 WO 03053884A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- explosive
- water
- resin
- oil
- ethylene
- Prior art date
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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
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B47/00—Compositions 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
- C06B47/14—Compositions 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
- C06B47/145—Water in oil emulsion type explosives in which a carbonaceous fuel forms the continuous phase
Definitions
- the present invention relates to explosives. More specifically, it relates to a water-in-oil emulsion explosive used for industrial blasting operations such as tunnel excavation, quarrying, and mining. Background art
- ANFO explosives nitrate oil explosives
- hydrous explosives are relatively safer than conventional dynamite because they do not contain explosive components in the composition, and have become widely used as industrial explosives.
- slurry explosives and emulsion explosives.
- Emulsion explosives are characterized by better moldability and better weatherability. Since this emulsion explosive was published in U.S. Patent No. 3,161,551 as a water-in-oil emulsion explosive, various improvements have been made, and at present water resistance and safety In this regard, some explosives have better performance than conventional explosives.
- the granules or granulation method of the water-in-oil emulsion explosive described in the above-mentioned publication is based on crystallizing an aqueous solution of an inorganic oxidizing agent in an emulsion, breaking the emulsion structure, and then granulating. Things.
- granules or granular water-in-oil emulsion explosives do not crystallize the oxidizing agent aqueous solution and are stable over time for several months.
- the explosive is stable so that the properties of the water-in-oil type emulsion explosive do not change for a long period of time so that the explosive can be used for machine loading.
- a granulated explosive is subjected to a load such as long-term storage or mechanical loading, the drug may agglomerate and may not be loosened during use, making it difficult to use. Therefore, it is desirable to use granular water-in-oil emulsion explosives that do not agglomerate even under heavy loads, such as long-term storage and mechanical loading, or that the agglomerates are easily loosened. Disclosure of the invention
- the present inventors have conducted intensive studies in order to solve such problems, and as a result, have replaced or partially substituted the entire or a part of the continuous phase component of the water-in-oil emulsion with an ethylene vinyl acetate polymer.
- the inventors have found that a solid explosive having appropriate strength and stable for several months or more can be obtained when contained in a continuous phase component to form a water-in-oil type emulsion explosive, thereby completing the present invention.
- the present invention provides:
- a water-in-oil emulsion explosive characterized by containing an ethylene-vinyl acetate copolymer in a continuous phase
- a water-in-oil emulsion explosive characterized by containing an oxidizing agent, oils, an ethylene-vinyl acetate polymer, an emulsifier, and fine hollow spheres;
- the continuous phase is an oil phase (fuel phase).
- a mixture containing both oils and an ethylene-vinyl acetate copolymer (hereinafter also referred to as EVA resin) is used.
- EVA resin ethylene-vinyl acetate copolymer
- the oil phase which is a continuous phase, may contain no oils in some cases, and may be formed of an EVA resin or a mixed resin composed of the resin and another resin;
- the EVA resin is preferably a resin which has a property of being cured or its viscosity lowered by heat, and which can be injection-molded when mixed with an oxidizing agent, water, an emulsifier, fine hollow spheres and, if necessary, an oil. More specifically, those having a number average molecular weight within the range of about 100 to 60,000 are usually used, and those having a molecular weight of about 100 to 50,000 are preferable. More preferably, the molecular weight is 2,000 or more, more preferably 10,000 or more, and preferably in the range of 40,000 or less.
- the EVA resin used in the present invention may be a copolymer containing other copolymer components as long as it contains an ethylene-vinyl acetate copolymer as a main component.
- the proportion of the ethylene vinyl acetate copolymer portion to the whole EVA resin is preferably 30 to 100%; more preferably 50 to 100%. More preferably, it is 70% to 10.0%. Most preferred is an ethylene-vinyl acetate copolymer substantially free of other copolymer components.
- the content of the ethylene-vinyl acetate copolymer with respect to the entire explosive of the present invention may be any amount as long as the effect of the present invention is exhibited, but is preferably 0.2% or more, more preferably 0.4% or more, and still more preferably. Is 0.6% or more, and 8% or less, more preferably 6% or less, and further preferably 4% or less. Although it depends on the type of the ethylene-vinyl acetate copolymer, the most preferable range is usually about 0.6 to 3%.
- the continuous phase is preferably a mixture containing an oil described below and an ethylene-vinyl acetate copolymer.
- the resin contained in the continuous phase may be an EVA resin alone, but may contain a resin other than the ethylene-vinyl acetate copolymer as long as the effects of the present invention are exhibited.
- Other resins preferably exhibit oil solubility or compatibility with oils.
- the other resin examples include a thermosetting resin, a thermoplastic resin, and a synthetic rubber.
- vulcanized rubber petroleum resin, phenolic resin, AAS resin, ABS resin, PET resin, urea resin, melamine resin, epoxy resin, unsaturated polyester resin, polyurethane resin, polyvinyl chloride, polyvinyl acetate
- examples thereof include a polyamide resin, a polyimide resin, and a polyethylene resin, but a resin that does not react with other components is preferable in order to maintain the stability of the water-in-oil emulsion.
- a thermosetting resin having a liquid or low melting point at room temperature or a thermoplastic resin which is solid at room temperature and exhibits fluidity when heated is preferable.
- phenol resin petroleum resin
- polyethylene polypropylene
- polybutylene polyisobutylene
- ethylene-vinyl acetate copolymer resin polybutadiene
- styrene-butadiene rubber etc.
- petroleum resins among these may or may not be hydrogenated Teatsu, for example aliphatic or G petroleum resin G fraction of the cracked oil fraction and the raw material, the C 9 fraction material use the aromatic or C 9 petroleum resin, both have a like GC 9 copolymer petroleum resins in the raw material within.
- resins made from the C5 fraction are, for example, copolymers such as isoprene, piperylene, and 2-methylbutene-1 and 2, and conjugated diolefins often have a cyclized structure. What is possessed is a typical example.
- the resin made from the G fraction is, for example, a copolymer containing styrene, vinyltoluene, a-methylstyrene, indene, or the like as a main component. It is. + ⁇ .
- n the number of repetitions.
- oil mixture means a mixture of EVA resin and oil or / and EVA resin unless otherwise specified.
- the continuous phase is formed in an oil mixture.
- the ratio of the EVA resin to the total amount of the oils and the EVA resin is not particularly limited as long as the effects of the present invention are achieved, but is usually 10% or more, preferably 20% or more. All may be EVA resin. More preferred, however, is when the EVA resin is 30-80% of the total oil mixture. When other resins are used in combination, it is preferable to use them together so that the EVA resin is contained in the above-mentioned lower limit or more and the total amount of the EVA resin and the other resin is not more than the above-mentioned upper limit.
- the preferred content of the EVA resin will vary slightly depending on the molecular weight of the EVA resin, A relatively small amount may be used, and a relatively high amount tends to be better for a low molecular weight.
- the number average molecular weight is greater than 10,000, preferably 12,000 or more, more preferably 20,000 or more, the content may be 60% or less, preferably 25% or less, based on the total amount described above.
- About 50% is in the case of a low molecular weight EVA resin having a number average molecular weight of about 2,000 to 3,000, its content is at least 50%, more preferably about 60 to 80%.
- the EVA resin melt at the production temperature.
- the number average molecular weight of the resin can be measured, for example, by gel permeation chromatography or the like.
- the explosive of the present invention usually contains oils. Oils that are commonly used in water-in-oil emulsion explosives can be used. Oils increase the emulsifiability of the emulsion and form a continuous phase with the EVA resin. Oils include petroleum oils such as light oil, kerosene, mineral oil, lubricating oil, heavy oil, petroleum waxes such as paraffin wax and microcrystalline wax, other hydrophobic vegetable oils, vegetable oils, animal oils, etc. Animal waxes can be used, and these can be used alone or in combination of two or more.
- the oil mixture containing the oil is contained in the explosive in an amount of usually 0.1 to 20%, preferably 1 to 10%.
- the amount of the oil mixture used is usually 0.1 in the explosive based on the total amount. % Or more, preferably 0.5% or more, more preferably 1% or more, and still more preferably 1.5% or more.
- the upper limit is usually about 10%, preferably 7% or less. A particularly preferred range is about 2 to 5%.
- emulsifiers used in the explosive of the present invention include emulsifiers commonly used in water-in-oil emulsion explosives, for example, those having 15 to 30 carbon atoms such as alkali metal stearate, ammonium stearate or calcium stearate. Degree of fatty acid salt
- alkali metal salts, earth metal salts and ammonium salts, etc. polyoxyethylene ethers, fatty acid esters, preferably fatty acid esters having 15 to 30 carbon atoms, such as sorbitan fatty acid esters And solzetol fatty acid esters. These are used as one kind or as a mixture of two or more kinds.
- the content of the emulsifier in the explosive is 0.1% or more, preferably 0.5% or more, more preferably 1% or more, and the upper limit is usually about 10%, preferably 7%. % Or less, more preferably 5% or less.
- the oxidizing agent used in the explosive of the present invention is preferably used as an aqueous solution thereof.
- the oxidizing agent include nitrates and perchlorates.
- Specific examples include alkali metal nitrates such as sodium nitrate, alkaline earth metal nitrates such as calcium nitrate, ammonium nitrate, ammonium nitrate, and sodium chlorate.
- Alkaline earth metal chlorates such as alkali metal chlorate, calcium chlorate, alkali metal perchlorates such as potassium perchlorate, alkaline earth metal perchlorates such as calcium perchlorate, And ammonium perchlorate. These can be used alone or in combination.
- oxidizing agents are ammonium nitrate and sodium nitrate.
- the oxidizing agent content in the oxidizing agent aqueous solution is preferably adjusted so that the crystallization temperature of the aqueous solution is 30 to 90 ° C. depending on the purpose of use and the like. Therefore, although it varies depending on the type of the oxidizing agent, it is usually 60 to 95%, preferably 70 to 93%, more preferably 85 to 92%.
- the aqueous solution of the oxidizing agent used in the present invention may, if desired, contain a water-soluble amine nitrate such as monomethylamine nitrate, monoethylamine nitrate, hydrazine nitrate or dimethylamine dinitrate, or a water-soluble alcohol such as methanolamine nitrate or ethanolamine nitrate. It is possible to add, as auxiliary sensitizers, nitrolamine nitrates and water-soluble ethylene glycol mononitrate.
- a water-soluble amine nitrate such as monomethylamine nitrate, monoethylamine nitrate, hydrazine nitrate or dimethylamine dinitrate
- a water-soluble alcohol such as methanolamine nitrate or ethanolamine nitrate. It is possible to add, as auxiliary sensitizers, nitrolamine nitrates and water-soluble ethylene glycol mononitrate.
- the oxidizing agent aqueous solution used in the present invention is suitably adjusted so that the crystal precipitation temperature is 30 to 90 ° C.
- the water content in the oxidizing agent aqueous solution is It is used in a proportion of usually 5 to 40%, preferably 7 to 30%, particularly preferably 8 to 15%, based on the total amount of the solution.
- a water-soluble organic solvent such as methyl alcohol, ethyl alcohol, formamide, ethylene glycol, and dalyserin can be used as an auxiliary solvent to lower the crystallization temperature of the oxidizing agent aqueous solution.
- the oxidizing agent aqueous solution (which may contain an auxiliary solvent) is the remainder of the explosive of the present invention except for the content of other components, and is preferably 60 to 97% based on the total amount. , More preferably in the range of 80-95%.
- the sensitivity performance of the explosive ranges from primer detonation to booster detonation. Can be adjusted.
- the density of the low density extender is usually 0.8 g / cc or less, preferably 0.5 g / cc or less, more preferably 0.3 gZc c or less, and in the case of an organic low density extender, 0.3 g / cc. / cc or less, and in some cases 0.05 g / cc or less can be used.
- the low-density extender any inert low-density one may be used, but a micro hollow sphere is preferable in order to obtain stable explosive performance.
- a micro hollow sphere for example, one or a mixture of two or more inorganic hollow spheres such as glass micro balloons and shirasu balloons, and organic hollow spheres such as expanded styrene and resin micro balloons are used. Resin microphone balloons are preferred, and glass microballoons are particularly preferred.
- the amount of the low-density extender varies widely depending on the application of the explosive and depends on the specific gravity of the micro hollow sphere, so it cannot be specified unconditionally, but usually the density of the explosive is 0.8 g / cc.
- the amount is preferably 0.9 g / cc or more, more preferably 1 gZcc or more, and is preferably used in an amount of 1.4 gZcc or less, preferably 1.3 g / cc or less.
- the preferred range of the compounding amount is about 0.1 to 10%, more preferably 1 to 8%, more preferably 1 to 6%, and in some cases, the optimal range is 2 to 5% based on the total amount of the explosive of the present invention. It is.
- the preferable blending amount is 1% or more, and in some cases, 2% or more, 8% or less, and more preferably 5% or less.
- the water-in-oil emulsion explosive of the present invention may contain metal powders such as aluminum powder and magnesium powder, and organic powders such as wood powder and starch. These are added Depending on the type of substance and the purpose of addition, it is usually contained in explosives in the range of 0 to 10%.
- the explosive of the present invention is manufactured, for example, as follows.
- the oxidizing agent and, if necessary, the auxiliary sensitizing agent are dissolved in water at about 85 to 95 ° C. to obtain an oxidizing agent aqueous solution.
- the oil mixture component eg, EVA resin and oils, if necessary, a resin other than EVA resin, etc.
- the emulsifier are sufficiently mixed with heat to obtain an oil mixture containing the emulsifier.
- the above-mentioned oxidizing agent aqueous solution is gradually added to the oil mixture heated to about 85 to 95 ° C. with sufficient stirring to obtain a water-in-oil emulsion base material.
- Emulsion explosives can be obtained.
- the obtained explosive can be obtained as a molded explosive of the present invention by transferring it to a molding machine while molding it in a state of fluidity or cooling it to room temperature and molding it.
- a part of the oil mixture component may be added when adding the microscopic hollow spheres.
- an oil and an emulsifier are mixed to form a water-in-oil emulsion, and EVA resin is added and mixed when adding minute hollow spheres to the emulsion.
- Emulsions may be used, and oils may be added and mixed when the micro hollow spheres are added.However, usually, as described above, the oil mixture component and the emulsifier are mixed to form an oil mixture containing the emulsifier. It is preferable to obtain a water-in-oil emulsion and add micro hollow spheres to it.
- the water-in-oil emulsion explosive of the present invention thus obtained is preferably used after being formed into an appropriate shape by a conventional method.
- the shape of the formed explosive of the present invention is not particularly limited, and the explosive may be formed into an arbitrary shape by a molding machine which can be used in any of spherical, columnar, disk-like, and prismatic shapes. It may be formed into any shape, but the size is preferably such that the maximum length (the length of the longest side or the maximum length) in the shape is 30 mm or less, more preferably 20 mm or less.
- the shortest length (the length of the shortest side or the shortest length) is preferably 1 mm or more, more preferably 3 mm or more.
- Examples of the method for producing the explosive of the present invention include a method using an extruder generally used, and a method in which a water-in-oil emulsion explosive is pulverized by a pulverizer or the like and then granulated by a granulator or the like.
- extrusion molding is preferred.
- a water-in-oil emulsion explosive is extruded through a perforated plate or screen to form a water-in-oil emulsion explosive into a rod shape, and then cut into appropriate lengths with a knife, wire, etc.
- a perforated plate or screen to form a water-in-oil emulsion explosive into a rod shape
- the length is l ⁇ 30mm, preferably about 5 ⁇ 10mm in diameter and about 3 ⁇ 20mm in length.
- the cylindrical explosive of the present invention can be manufactured by a method as simple as a conventional water-in-oil emulsion explosive.
- aqueous solution of oxidizing agent consisting of 75.0 parts of ammonium nitrate, 4.8 parts of sodium nitrate and 6.6 parts of water at 90 ° C consisting of 1.5 parts of microcrystalline wax, 1.5 parts of microcrystalline wax, ethylene-vinyl acetate copolymer resin (Mitsui DuPont Polypropylene) Made by Chemical Co., Ltd., trade name: Evaflexs P-2807; number average molecular weight 20000-30000, melt flow rate 15 g / 10min, 1.4 parts, sorbitan monooleate 2. 9 parts mixture In addition, the mixture was sufficiently stirred and mixed to obtain a water-in-oil emulsion.
- oxidizing agent consisting of 75.0 parts of ammonium nitrate, 4.8 parts of sodium nitrate and 6.6 parts of water at 90 ° C consisting of 1.5 parts of microcrystalline wax, 1.5 parts of microcrystalline wax, ethylene-vinyl acetate copolymer resin (Mitsui DuPont Poly
- a 90 ° C oxidizing agent solution consisting of 75.0 parts of ammonium nitrate, 4.8 parts of sodium nitrate and 10.6 parts of water was added to 1.5 parts of microcrystalline wax, 1.5 parts of ethylene vinyl acetate copolymer resin (Tosoichisha Co., Ltd.) Product name: Ultracene 720; number average molecular weight approx. 37,000, melt flow rate: 150 g / 10 min.) 1. 4 parts, sorbitan monooleate 2. Add to 9 parts of the mixture, mix well and mix well Thus, a water-in-oil emulsion was obtained. Glass microballoons 3.8 as micro hollow spheres
- a 90 ° C aqueous solution of an oxidizing agent consisting of 75.0 parts of ammonium nitrate, 4.8 parts of sodium nitrate and 10.6 parts of water was added to a mixture of 3.8 parts of microcrystalline wax and 2.0 parts of sorbitan monooleate. After sufficiently stirring and mixing, a water-in-oil emulsion was obtained. To this, 3.8 parts (specific gravity: 0.25 g / cc) of the same glass microballoons as in the example as micro hollow spheres were added and mixed by stirring to obtain a water-in-oil type emulsion explosive for comparison.
- This water-in-oil type emulsion explosive was molded by an extruder with a die of 8 mm in diameter, and cut with a knife to a length of 1 Omm to obtain a comparative explosive.
- the specific gravity of the obtained explosive was 1.17.
- Table 1 shows the composition ratios of the water-in-oil emulsion explosives obtained in Examples 1 to 3 and Comparative Example 1. Composition ratio
- the explosives obtained in Examples 1 to 2 and Comparative Example 1 were charged into a steel pipe having an inner diameter of 48 mm, a length of lm, and a thickness of 5 mm using an air-loading machine. It was detonated using 50 g of a water-containing explosive (trade name: Artex) manufactured by K.K., and the detonation velocity was measured by the Doritish method. After the same steel pipe was filled with water in advance, each explosive was loaded using an air-spotting machine in the same manner as above, and the detonation velocity in the water hole was measured.
- a water-containing explosive trade name: Artex
- the molded explosive obtained above was stored in a vinyl bag so as to have a thickness of about 15 to 20 cm, and stored at room temperature for 6 months and 1 year.
- the detonation rate was measured in the drying hole and the water hole in the same manner as above. The results are shown in Table 2.
- the explosive of the present invention did not harden after storage for one year and had the initial performance when stored at room temperature under no load.
- the explosive of the comparative example could measure the detonation speed immediately after production, but even after storage for 6 months at room temperature under non-weighted conditions, it became a lump, as shown in Table 2. Detonation velocity measurement was not possible.
- the water-in-oil emulsion explosive of the present invention is hardly deformed or agglomerated by a load, and can be easily disintegrated to the extent that it causes light partial solidification even under long-term storage of half a year to one year under a load. It has long-term stability over time and has excellent water resistance. Therefore, when the explosive of the present invention is appropriately molded, it can be used for air charging or the like. It can be easily loaded into blast holes using a loading machine, and can be used in water holes without deteriorating explosive performance. The residual gas composition after blasting is also better than that of ANF II explosives.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/499,053 US20050155682A1 (en) | 2001-12-20 | 2002-12-18 | Explosive |
CA002470861A CA2470861A1 (en) | 2001-12-20 | 2002-12-18 | Explosive |
EP02790802A EP1457474A4 (en) | 2001-12-20 | 2002-12-18 | EXPLOSIVE |
AU2002366768A AU2002366768A1 (en) | 2001-12-20 | 2002-12-18 | Explosive |
KR1020047009463A KR100824932B1 (ko) | 2001-12-20 | 2002-12-18 | 폭약 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001387662 | 2001-12-20 | ||
JP2001/387662 | 2001-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003053884A1 true WO2003053884A1 (fr) | 2003-07-03 |
Family
ID=19188086
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2002/013222 WO2003053884A1 (fr) | 2001-12-20 | 2002-12-18 | Explosif |
Country Status (8)
Country | Link |
---|---|
US (1) | US20050155682A1 (ja) |
EP (1) | EP1457474A4 (ja) |
KR (1) | KR100824932B1 (ja) |
CN (1) | CN1291952C (ja) |
AU (1) | AU2002366768A1 (ja) |
CA (1) | CA2470861A1 (ja) |
TW (1) | TWI289547B (ja) |
WO (1) | WO2003053884A1 (ja) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101152992B (zh) * | 2006-09-29 | 2011-05-04 | 鞍钢集团矿业公司 | 一种炸药混装车上生产的乳化炸药 |
CN101152993B (zh) * | 2006-09-29 | 2011-08-17 | 鞍钢集团矿业公司 | 用于乳化炸药混装车的乳化剂及其合成方法 |
CN103951535A (zh) * | 2014-04-29 | 2014-07-30 | 湖北同一石油化工有限公司 | 高温敏化特种专用蜡及其制作方法 |
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US9085727B2 (en) | 2006-12-08 | 2015-07-21 | Schlumberger Technology Corporation | Heterogeneous proppant placement in a fracture with removable extrametrical material fill |
US8757259B2 (en) | 2006-12-08 | 2014-06-24 | Schlumberger Technology Corporation | Heterogeneous proppant placement in a fracture with removable channelant fill |
CN102731228A (zh) * | 2012-07-03 | 2012-10-17 | 保利民爆济南科技有限公司 | 一种乳化炸药快速敏化剂 |
CN103183575B (zh) * | 2013-03-07 | 2015-09-09 | 许畅 | 乳化炸药复合油相 |
CN103922874B (zh) * | 2014-04-15 | 2015-11-25 | 葛洲坝易普力股份有限公司 | 原生聚苯乙烯颗粒作为物理敏化剂在混装乳化炸药中的应用和混装乳化炸药及其制备方法 |
WO2016100160A1 (en) | 2014-12-15 | 2016-06-23 | Dyno Nobel Inc. | Explosive compositions and related methods |
CN105111033A (zh) * | 2015-08-20 | 2015-12-02 | 福建海峡科化股份有限公司 | 一种多孔粒状铵油炸药及其制备方法 |
EP3239120A1 (en) * | 2016-04-27 | 2017-11-01 | Clariant International Ltd | Water resistance additive for ammonium nitrate - fuel oil (anfo) explosives |
CN107867962B (zh) * | 2017-08-18 | 2019-11-05 | 湖北航天化学技术研究所 | 一种热塑性复合固体推进剂及其制备方法 |
CN114057530B (zh) * | 2021-12-17 | 2022-07-15 | 南京晓庄学院 | 一种乳化炸药动态稳定性促进剂 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2138800A (en) * | 1983-02-24 | 1984-10-31 | Nippon Kayaku Kk | Water-in-oil emulsion explosive |
JP2001172096A (ja) * | 1999-12-17 | 2001-06-26 | Asahi Kasei Corp | 固形エマルション爆薬組成物及びその製造方法 |
JP2002003804A (ja) * | 2000-06-19 | 2002-01-09 | Nippon Nsc Ltd | ホットメルト接着剤 |
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US4113811A (en) * | 1975-07-02 | 1978-09-12 | Dynamit Nobel Aktiengesellschaft | Process for the production of flexible explosive formed charges |
CA1188898A (en) * | 1983-04-21 | 1985-06-18 | Howard A. Bampfield | Water-in-wax emulsion blasting agents |
EP0238210A3 (en) * | 1986-03-14 | 1989-05-24 | Imperial Chemical Industries Plc | Solid explosive composition |
GB8614228D0 (en) * | 1986-06-11 | 1986-10-29 | Ici Plc | Explosive compound |
US4736683A (en) * | 1986-08-05 | 1988-04-12 | Exxon Chemical Patents Inc. | Dry ammonium nitrate blasting agents |
-
2002
- 2002-12-18 KR KR1020047009463A patent/KR100824932B1/ko not_active IP Right Cessation
- 2002-12-18 CA CA002470861A patent/CA2470861A1/en not_active Abandoned
- 2002-12-18 EP EP02790802A patent/EP1457474A4/en not_active Withdrawn
- 2002-12-18 AU AU2002366768A patent/AU2002366768A1/en not_active Abandoned
- 2002-12-18 US US10/499,053 patent/US20050155682A1/en not_active Abandoned
- 2002-12-18 WO PCT/JP2002/013222 patent/WO2003053884A1/ja active Application Filing
- 2002-12-18 CN CNB028254392A patent/CN1291952C/zh not_active Expired - Fee Related
- 2002-12-19 TW TW091136615A patent/TWI289547B/zh not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2138800A (en) * | 1983-02-24 | 1984-10-31 | Nippon Kayaku Kk | Water-in-oil emulsion explosive |
JP2001172096A (ja) * | 1999-12-17 | 2001-06-26 | Asahi Kasei Corp | 固形エマルション爆薬組成物及びその製造方法 |
JP2002003804A (ja) * | 2000-06-19 | 2002-01-09 | Nippon Nsc Ltd | ホットメルト接着剤 |
Non-Patent Citations (1)
Title |
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See also references of EP1457474A4 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101152992B (zh) * | 2006-09-29 | 2011-05-04 | 鞍钢集团矿业公司 | 一种炸药混装车上生产的乳化炸药 |
CN101152993B (zh) * | 2006-09-29 | 2011-08-17 | 鞍钢集团矿业公司 | 用于乳化炸药混装车的乳化剂及其合成方法 |
CN103951535A (zh) * | 2014-04-29 | 2014-07-30 | 湖北同一石油化工有限公司 | 高温敏化特种专用蜡及其制作方法 |
Also Published As
Publication number | Publication date |
---|---|
CN1606537A (zh) | 2005-04-13 |
TWI289547B (en) | 2007-11-11 |
AU2002366768A1 (en) | 2003-07-09 |
KR20040075008A (ko) | 2004-08-26 |
EP1457474A4 (en) | 2006-08-09 |
CA2470861A1 (en) | 2003-07-03 |
CN1291952C (zh) | 2006-12-27 |
KR100824932B1 (ko) | 2008-04-28 |
TW200301236A (en) | 2003-07-01 |
US20050155682A1 (en) | 2005-07-21 |
EP1457474A1 (en) | 2004-09-15 |
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