CN105949013A - Preparation method of mixed emulsion explosive - Google Patents

Preparation method of mixed emulsion explosive Download PDF

Info

Publication number
CN105949013A
CN105949013A CN201610286932.6A CN201610286932A CN105949013A CN 105949013 A CN105949013 A CN 105949013A CN 201610286932 A CN201610286932 A CN 201610286932A CN 105949013 A CN105949013 A CN 105949013A
Authority
CN
China
Prior art keywords
aqueous phase
oil
tank
weight
percentage
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
CN201610286932.6A
Other languages
Chinese (zh)
Inventor
周勇
邓波
唐桥梁
杨海量
向元峰
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.)
China Harbour Engineering Co Ltd
Original Assignee
China Harbour Engineering 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 China Harbour Engineering Co Ltd filed Critical China Harbour Engineering Co Ltd
Priority to CN201610286932.6A priority Critical patent/CN105949013A/en
Publication of CN105949013A publication Critical patent/CN105949013A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • C06B31/00Compositions containing an inorganic nitrogen-oxygen salt
    • C06B31/28Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
    • C06B31/285Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with fuel oil, e.g. ANFO-compositions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Inorganic Chemistry (AREA)
  • Lubricants (AREA)

Abstract

The invention provides a preparation method of a mixed emulsion explosive. The method comprises the following steps: 1, preparing a water phase: sequentially adding metered ammonium nitrate, sodium nitrate and citric acid to a water phase dissolving tank; 2, preparing an oil phase: sequentially adding metered machine oil, diesel oil and an emulsifier to an oil phase dissolving tank; 3, carrying out primary emulsification; 4, carrying out secondary emulsification; 5, cooling a mixed solution in a secondary emulsifying machine to 30-40DEG C; 6, charging: pumping the cooled mixed solution to a charging machine, and pumping a foaming agent comprising water and sodium nitrite according to a weight ratio of 1:12 to a charging tube in the charging process; and 7, sensitizing. The preparation method of the mixed emulsion explosive has the characteristics of simple process, high processing efficiency and low production cost, and the emulsion explosive prepared through the method has the characteristics of ideal explosion effect and low storage cost.

Description

A kind of preparation method of the mixed loading emulsion explosive
Technical field
The present invention relates to explosive preparation field, the preparation method of a kind of the mixed loading emulsion explosive.
Background technology
Emulsion is the principal item of current commercial explosive, is the developing direction of industry promotion.Mainly comprising of this explosive It is using ammonium nitrate, sodium nitrate, water as dispersion phase, with oil phase as continuous phase, forms water in oil structure by emulsifying agent. It is relatively big that the emulsifying base so formed does not has cap-sensitivity density, reduces density by adding the regulation of a certain amount of sensitizer, Improve sensitivity.
The Initiation principle of emulsion is referred to as scorching hot core principle, is also hot spot theory.Sensitizer can explode in emulsifying after adding Forming a lot of scattered minute bubbles in medicine, after blasting cap initiation, shock wave is to explosive effect, the bubble in compression explosive, bubble quilt Compression can form high temperature hotspot so that explosive initiation.
Emulsion weak effect, complex process and cost that current existing emulsion technique prepares are high.
Summary of the invention
It is an object of the invention to provide the preparation method of a kind of the mixed loading emulsion explosive, step includes:
1) aqueous phase configuration
1.1. according to percentage by weight, the water of 11.5% is pumped in aqueous phase dissolved tank, carry out after steam is heated to 70-80 DEG C Start agitator;
1.2. according to percentage by weight, the ammonium nitrate of 73.5% is put in described aqueous phase dissolved tank;
1.3. according to percentage by weight, the sodium nitrate of 8% is put in described aqueous phase dissolved tank;
1.4. according to percentage by weight, the citric acid of 0.2% is put in described aqueous phase dissolved tank;
1.5. steam heats described aqueous phase dissolved tank, and heating-up temperature is: 90-110 DEG C, and heat time heating time is: 80-100Min;
1.6. the material pumping in described aqueous phase dissolved tank is filtered to filter, the product pump after then filtering Deliver to aqueous phase holding vessel;
1.7. described aqueous phase accumulator tank temperature is controlled at 100-105 DEG C;
2) oil phase configuration
2.1. oil phase dissolving tank is carried out steam and be heated to 85-90 DEG C;
2.2. according to percentage by weight, the machine oil of 3% is put in described oil phase dissolving tank;
2.3. according to percentage by weight, the diesel oil of 1.5% is put in described oil phase dissolving tank;
2.4. according to percentage by weight, the emulsifying agent of 2% is put in described oil phase dissolving tank;
2.5. steam heats described oil phase dissolving tank, and heating-up temperature is: 90-95 DEG C, and heat time heating time is: 20-30min;
2.6. agitator uniform stirring oil-phase solution is started;
2.7. the material pumping in described oil phase dissolving tank is filtered to filter, the product pump after then filtering Deliver to oil phase holding vessel;
2.8. described oil phase accumulator tank temperature is controlled at 90-100 DEG C;
3) one-level emulsifying
3.1. oil-phase solution is pumped in one-level mulser according to the speed of 1.17/min;
3.2., after oil-phase solution all pumps and terminates, aqueous phase solution is pumped to one-level mulser according to the speed of 650l/h In;
3.3., after aqueous phase solution all pumps and terminates, mulser is opened;
3.4. the one-level mulser operation time is: 20-30min, emulsifying temperature is: 80-90 DEG C;
4) two grades of emulsifying
Mixed solution in mulser is pumped in two grades of mulsers carry out emulsifying, and two grades of mulsers run the times and are: 50-60min, emulsifying temperature is 70-80 DEG C;
5) cooling
The mixed solution of two grades of mulsers is cooled down, mixed solution temperature is down to 30-40 DEG C;
6) powder charge
Mixed solution after cooling is pumped to charging machine, during powder charge, is water by components by weight percent proportioning simultaneously: Sodium nitrite is: the foaming agent of 1:12 pumps into powder charge pipe by lubricating pump;
7) sensitization
Powder charge pipe is carried out the sensitization under water of 5-10min.
Prioritization scheme is: the mesh size of described filter is GF/W0.3/0.125.
Prioritization scheme is: the colloid temperature of described two grades of mulsers outlet is 90-100 DEG C.
Prioritization scheme is: quick-fried body is made up of nitrogelatin and detonator, and described nitrogelatin is placed at the bottom of the hole of described ignition body.
Prioritization scheme is to increase the sand pocket counterweight of 5 on described ignition body.
The preparation method of the mixed loading emulsion explosive of the present invention, has technical process simple, and working (machining) efficiency is high, and production cost is low Feature, the emulsion prepared by this technique, there is explosive effect preferable, the feature that storage cost is low.
Detailed description of the invention
Below in conjunction with detailed description of the invention, the present invention is described in further detail, to make those skilled in the art with reference to explanation Book word can be implemented according to this.
Should be appreciated that used herein such as " have ", " comprising " and " including " term do not allot one or more its Its element or the existence of a combination thereof or interpolation.
Embodiment 1
It is an object of the invention to provide the preparation method of a kind of the mixed loading emulsion explosive, step includes:
1) aqueous phase configuration
1.1. according to percentage by weight, the water of 11.5% is pumped in aqueous phase dissolved tank, carry out opening after steam is heated to 70 DEG C Dynamic agitator;
1.2. according to percentage by weight, the ammonium nitrate of 73.5% is put in described aqueous phase dissolved tank;
1.3. according to percentage by weight, the sodium nitrate of 8% is put in described aqueous phase dissolved tank;
1.4. according to percentage by weight, the citric acid of 0.2% is put in described aqueous phase dissolved tank;
1.5. steam heats described aqueous phase dissolved tank, and heating-up temperature is: 90 DEG C, and heat time heating time is: 80Min;
1.6. the material pumping in described aqueous phase dissolved tank is filtered to filter, the product pump after then filtering Deliver to aqueous phase holding vessel;
1.7. described aqueous phase accumulator tank temperature is controlled at 100 DEG C;
2) oil phase configuration
2.1. oil phase dissolving tank is carried out steam and be heated to 85 DEG C;
2.2. according to percentage by weight, the machine oil of 3% is put in described oil phase dissolving tank;
2.3. according to percentage by weight, the diesel oil of 1.5% is put in described oil phase dissolving tank;
2.4. according to percentage by weight, the emulsifying agent of 2% is put in described oil phase dissolving tank;
2.5. steam heats described oil phase dissolving tank, and heating-up temperature is: 90 DEG C, and heat time heating time is: 20min;
2.6. agitator uniform stirring oil-phase solution is started;
2.7. the material pumping in described oil phase dissolving tank is filtered to filter, the product pump after then filtering Deliver to oil phase holding vessel;
2.8. described oil phase accumulator tank temperature is controlled at 90 DEG C;
3) one-level emulsifying
3.1. oil-phase solution is pumped in one-level mulser according to the speed of 1.17/min;
3.2., after oil-phase solution all pumps and terminates, aqueous phase solution is pumped to one-level mulser according to the speed of 650l/h In;
3.3., after aqueous phase solution all pumps and terminates, mulser is opened;
3.4. the one-level mulser operation time is: 20min, emulsifying temperature is: 80 DEG C;
4) two grades of emulsifying
Mixed solution in mulser is pumped in two grades of mulsers carry out emulsifying, and two grades of mulsers run the times and are: 50min, emulsifying temperature is 70 DEG C;
5) cooling
The mixed solution of two grades of mulsers is cooled down, mixed solution temperature is down to 30 DEG C;
6) powder charge
Mixed solution after cooling is pumped to charging machine, during powder charge, is water by components by weight percent proportioning simultaneously: Sodium nitrite is: the foaming agent of 1:12 pumps into powder charge pipe by lubricating pump;
7) sensitization
Powder charge pipe is carried out the sensitization under water of 5min.
The mesh size of described filter is GF/W0.3/0.125.
The colloid temperature of described two grades of mulsers outlet is 90 DEG C.
Quick-fried body is made up of nitrogelatin and detonator, and described nitrogelatin is placed at the bottom of the hole of described ignition body.
The sand pocket counterweight of 5 in increasing by one on described ignition body.
Embodiment 2
It is an object of the invention to provide the preparation method of a kind of the mixed loading emulsion explosive, step includes:
1) aqueous phase configuration
1.1. according to percentage by weight, the water of 11.5% is pumped in aqueous phase dissolved tank, carry out opening after steam is heated to 80 DEG C Dynamic agitator;
1.2. according to percentage by weight, the ammonium nitrate of 73.5% is put in described aqueous phase dissolved tank;
1.3. according to percentage by weight, the sodium nitrate of 8% is put in described aqueous phase dissolved tank;
1.4. according to percentage by weight, the citric acid of 0.2% is put in described aqueous phase dissolved tank;
1.5. steam heats described aqueous phase dissolved tank, and heating-up temperature is: 110 DEG C, and heat time heating time is: 100Min;
1.6. the material pumping in described aqueous phase dissolved tank is filtered to filter, the product pump after then filtering Deliver to aqueous phase holding vessel;
1.7. described aqueous phase accumulator tank temperature is controlled at 105 DEG C;
2) oil phase configuration
2.1. oil phase dissolving tank is carried out steam and be heated to 90 DEG C;
2.2. according to percentage by weight, the machine oil of 3% is put in described oil phase dissolving tank;
2.3. according to percentage by weight, the diesel oil of 1.5% is put in described oil phase dissolving tank;
2.4. according to percentage by weight, the emulsifying agent of 2% is put in described oil phase dissolving tank;
2.5. steam heats described oil phase dissolving tank, and heating-up temperature is: 95 DEG C, and heat time heating time is: 30min;
2.6. agitator uniform stirring oil-phase solution is started;
2.7. the material pumping in described oil phase dissolving tank is filtered to filter, the product pump after then filtering Deliver to oil phase holding vessel;
2.8. described oil phase accumulator tank temperature is controlled at 100 DEG C;
3) one-level emulsifying
3.1. oil-phase solution is pumped in one-level mulser according to the speed of 1.17/min;
3.2., after oil-phase solution all pumps and terminates, aqueous phase solution is pumped to one-level mulser according to the speed of 650l/h In;
3.3., after aqueous phase solution all pumps and terminates, mulser is opened;
3.4. the one-level mulser operation time is: 30min, emulsifying temperature is: 90 DEG C;
4) two grades of emulsifying
Mixed solution in mulser is pumped in two grades of mulsers carry out emulsifying, and two grades of mulsers run the times and are: 50-60min, emulsifying temperature is 80 DEG C;
5) cooling
The mixed solution of two grades of mulsers is cooled down, mixed solution temperature is down to 40 DEG C;
6) powder charge
Mixed solution after cooling is pumped to charging machine, during powder charge, is water by components by weight percent proportioning simultaneously: Sodium nitrite is: the foaming agent of 1:12 pumps into powder charge pipe by lubricating pump;
7) sensitization
Powder charge pipe is carried out the sensitization under water of 10min.
The mesh size of described filter is GF/W0.3/0.125.
The colloid temperature of described two grades of mulsers outlet is 100 DEG C.
Quick-fried body is made up of nitrogelatin and detonator, and described nitrogelatin is placed at the bottom of the hole of described ignition body.
The sand pocket counterweight of 5 in increasing by one on described ignition body.
Although embodiment of the present invention are disclosed as above, but it is not restricted in description and embodiment listed fortune With, it can be applied to various applicable the field of the invention completely, for those skilled in the art, and can be easily Realizing other amendment, therefore under the general concept limited without departing substantially from claim and equivalency range, the present invention does not limit In specific details.

Claims (5)

1. the preparation method of a mixed loading emulsion explosive, it is characterised in that step includes:
1) aqueous phase configuration
1.1. according to percentage by weight, the water of 11.5% is pumped in aqueous phase dissolved tank, carry out after steam is heated to 70-80 DEG C Start agitator;
1.2. according to percentage by weight, the ammonium nitrate of 73.5% is put in described aqueous phase dissolved tank;
1.3. according to percentage by weight, the sodium nitrate of 8% is put in described aqueous phase dissolved tank;
1.4. according to percentage by weight, the citric acid of 0.2% is put in described aqueous phase dissolved tank;
1.5. steam heats described aqueous phase dissolved tank, and heating-up temperature is: 90-110 DEG C, and heat time heating time is: 80-100Min;
1.6. the material pumping in described aqueous phase dissolved tank is filtered to filter, the product pump after then filtering Deliver to aqueous phase holding vessel;
1.7. described aqueous phase accumulator tank temperature is controlled at 100-105 DEG C;
2) oil phase configuration
2.1. oil phase dissolving tank is carried out steam and be heated to 85-90 DEG C;
2.2. according to percentage by weight, the machine oil of 3% is put in described oil phase dissolving tank;
2.3. according to percentage by weight, the diesel oil of 1.5% is put in described oil phase dissolving tank;
2.4. according to percentage by weight, the emulsifying agent of 2% is put in described oil phase dissolving tank;
2.5. steam heats described oil phase dissolving tank, and heating-up temperature is: 90-95 DEG C, and heat time heating time is: 20-30min;
2.6. agitator uniform stirring oil-phase solution is started;
2.7. the material pumping in described oil phase dissolving tank is filtered to filter, the product pump after then filtering Deliver to oil phase holding vessel;
2.8. described oil phase accumulator tank temperature is controlled at 90-100 DEG C;
3) one-level emulsifying
3.1. oil-phase solution is pumped in one-level mulser according to the speed of 1.17/min;
3.2., after oil-phase solution all pumps and terminates, aqueous phase solution is pumped to one-level mulser according to the speed of 650l/h In;
3.3., after aqueous phase solution all pumps and terminates, mulser is opened;
3.4. the one-level mulser operation time is: 20-30min, emulsifying temperature is: 80-90 DEG C;
4) two grades of emulsifying
Mixed solution in mulser is pumped in two grades of mulsers carry out emulsifying, and two grades of mulsers run the times and are: 50-60min, emulsifying temperature is 70-80 DEG C;
5) cooling
The mixed solution of two grades of mulsers is cooled down, mixed solution temperature is down to 30-40 DEG C;
6) powder charge
Mixed solution after cooling is pumped to charging machine, during powder charge, is water by components by weight percent proportioning simultaneously: Sodium nitrite is: the foaming agent of 1:12 pumps into powder charge pipe by lubricating pump;
7) sensitization
Powder charge pipe is carried out the sensitization under water of 5-10min.
The preparation method of the mixed loading emulsion explosive the most according to claim 1, it is characterised in that the mesh chi of described filter Very little for GF/W0.3/0.125.
The preparation method of the mixed loading emulsion explosive the most according to claim 1, it is characterised in that described two grades of mulsers outlet Colloid temperature be 90-100 DEG C.
The preparation method of the mixed loading emulsion explosive the most according to claim 1, it is characterised in that ignite body by nitrogelatin and Detonator forms, and described nitrogelatin is placed at the bottom of the hole of described ignition body.
The preparation method of the mixed loading emulsion explosive the most according to claim 1, it is characterised in that increase by one on described ignition body The sand pocket counterweight of 5 in individual.
CN201610286932.6A 2016-05-03 2016-05-03 Preparation method of mixed emulsion explosive Pending CN105949013A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610286932.6A CN105949013A (en) 2016-05-03 2016-05-03 Preparation method of mixed emulsion explosive

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610286932.6A CN105949013A (en) 2016-05-03 2016-05-03 Preparation method of mixed emulsion explosive

Publications (1)

Publication Number Publication Date
CN105949013A true CN105949013A (en) 2016-09-21

Family

ID=56913445

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610286932.6A Pending CN105949013A (en) 2016-05-03 2016-05-03 Preparation method of mixed emulsion explosive

Country Status (1)

Country Link
CN (1) CN105949013A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114768618A (en) * 2022-05-06 2022-07-22 山西省民爆集团有限公司 Rapid preparation method of composite oil phase for preparing emulsion explosive

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4525225A (en) * 1984-03-05 1985-06-25 Atlas Powder Company Solid water-in-oil emulsion explosives compositions and processes
CN1336355A (en) * 2000-08-02 2002-02-20 南京理工大学 Coal mine allowable powdered emulsified explosive and its production process
CN102173967A (en) * 2011-01-17 2011-09-07 广东宏大爆破股份有限公司 Emulsion explosive and preparation method thereof
CN102515988A (en) * 2011-12-09 2012-06-27 煤炭科学研究总院爆破技术研究所 Method for preparation of emulsion explosive by using waste explosives
CN103626615A (en) * 2013-12-19 2014-03-12 宜兴市阳生化工有限公司 MY type colloid emulsified civil explosive and production process thereof
CN104262067A (en) * 2014-10-20 2015-01-07 张亦彬 Method for preparing emulsion explosive by high-temperature sensitization
CN105001026A (en) * 2015-07-17 2015-10-28 刘发利 On-site mixed loading emulsion explosive and preparation method thereof
CN105218282A (en) * 2015-08-25 2016-01-06 宜兴市阳生化工有限公司 Gluey emulsion explosive of a kind of low temperature resistant water resisting property and preparation method thereof

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4525225A (en) * 1984-03-05 1985-06-25 Atlas Powder Company Solid water-in-oil emulsion explosives compositions and processes
CN1336355A (en) * 2000-08-02 2002-02-20 南京理工大学 Coal mine allowable powdered emulsified explosive and its production process
CN102173967A (en) * 2011-01-17 2011-09-07 广东宏大爆破股份有限公司 Emulsion explosive and preparation method thereof
CN102515988A (en) * 2011-12-09 2012-06-27 煤炭科学研究总院爆破技术研究所 Method for preparation of emulsion explosive by using waste explosives
CN103626615A (en) * 2013-12-19 2014-03-12 宜兴市阳生化工有限公司 MY type colloid emulsified civil explosive and production process thereof
CN104262067A (en) * 2014-10-20 2015-01-07 张亦彬 Method for preparing emulsion explosive by high-temperature sensitization
CN105001026A (en) * 2015-07-17 2015-10-28 刘发利 On-site mixed loading emulsion explosive and preparation method thereof
CN105218282A (en) * 2015-08-25 2016-01-06 宜兴市阳生化工有限公司 Gluey emulsion explosive of a kind of low temperature resistant water resisting property and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114768618A (en) * 2022-05-06 2022-07-22 山西省民爆集团有限公司 Rapid preparation method of composite oil phase for preparing emulsion explosive

Similar Documents

Publication Publication Date Title
CN102001901B (en) Method for manufacturing allowable emulsion explosive for coal mine
CN104109058B (en) Method for manufacturing on-site mixed emulsion explosive
CN104311373B (en) Three-level allowed for use in coal mines safety and environmental protection emulsion and preparation method thereof
CN102173967B (en) Emulsion explosive and preparation method thereof
CN108911934A (en) Foaming agent for emulsion explosive and the emulsion for using the foaming agent
CN102997767B (en) Field emulsion explosive mixing and charging system and charging method suitable for underground engineering
CN105949013A (en) Preparation method of mixed emulsion explosive
CN104311374A (en) Novel sensitization bubble carrier colloidal emulsion explosive and preparation method thereof
CN101328099B (en) Gel type emulsion explosive and preparation thereof
CN103626615A (en) MY type colloid emulsified civil explosive and production process thereof
CN101823926A (en) Preparation process of emulsion explosive
CN101357873B (en) Continuous technique for preparing emulsifying explosive and charging
CN106916042A (en) A kind of package-type emulsifying ammonium nitrate fuel explosive and preparation method thereof
CN104803814A (en) Intermediate-temperature-sensitized emulsion explosive and preparation method thereof
CN103113172B (en) Opencast emulsion explosive and preparation method thereof
CN102432407A (en) Magnesium hydride type hydrogen-stored emulsion explosive
CN102603437A (en) Method for manufacturing emulsion explosive with swill-cooked dirty oil
CN105712809B (en) Heat-sensitized emulsion and preparation method thereof
EP1002777B1 (en) Process and mechanism for in situ sensitization of aqueous explosives
CN105837387B (en) A kind of anti-desensitization type emulsion and preparation method thereof
CN102731223A (en) Method for producing emulsion explosive by using resin microspheres and dedicated emulsion sensitization machine thereof
CN101786932A (en) Oil-in-water powdery emulsion explosive, preparation method and application thereof
CN106673928A (en) High-temperature sensitized emulsion explosives and preparation method thereof
CN1325441C (en) High-energy colloidal focus medicinal column and production thereof
CN106518579A (en) Low-medium temperature chemical sensitization formula technology of emulsion explosive stable in performance

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20160921