CN110357151A - A kind of method of explosive synthesizing nano composite oxides - Google Patents

A kind of method of explosive synthesizing nano composite oxides Download PDF

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Publication number
CN110357151A
CN110357151A CN201910538103.6A CN201910538103A CN110357151A CN 110357151 A CN110357151 A CN 110357151A CN 201910538103 A CN201910538103 A CN 201910538103A CN 110357151 A CN110357151 A CN 110357151A
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CN
China
Prior art keywords
destructor
explosion
nano composite
powder
explosive
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Pending
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CN201910538103.6A
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Chinese (zh)
Inventor
李增源
钱青
谢兴华
谢亮
张庆玉
吕严龙
孙艳菊
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Anhui University of Science and Technology
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Anhui University of Science and Technology
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Priority to CN201910538103.6A priority Critical patent/CN110357151A/en
Publication of CN110357151A publication Critical patent/CN110357151A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G19/00Compounds of tin
    • C01G19/02Oxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G23/00Compounds of titanium
    • C01G23/04Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G51/00Compounds of cobalt
    • C01G51/04Oxides; Hydroxides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G9/00Compounds of zinc
    • C01G9/02Oxides; Hydroxides
    • C01G9/03Processes of production using dry methods, e.g. vapour phase processes
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • Y02P20/133Renewable energy sources, e.g. sunlight

Abstract

The present invention relates to a kind of explosion methods to synthesize nano composite oxide, by being exploded in a limited space using explosive, generate high temperature and pressure, can continue that secondary or even multiple reaction occurs, various metals powder can be made to be converted to nano composite oxide, gained nano composite oxide is sieved, the nano composite oxide that the height that partial size is 20-100nm mixes can be obtained.Single oxidation physical performance may not have the whole requirements for making certain material, a kind of good means is then needed to obtain two kinds or even a variety of composite oxides at this time.The present invention can be properly arrived at this and want ball, and simple process, and obtained good quality of product is worthy to be popularized.

Description

A kind of method of explosive synthesizing nano composite oxides
Technical field
The present invention relates to a kind of novel processing steps of explosive manner synthesis nano composite oxide.
Background technique
There is no any single substance to be perfectly, almost all of quality material is all the mixing of two or more substances Object.Such as, our common white pigments have titanium white and zinc white.The ingredient of titanium white is titanium oxide, there is the stronger advantage of covering power, but Color is easy jaundice.The chemical component of zinc white is zinc oxide, and covering power is easy to change not as good as titanium white, but not, thus, if being mixed Uniformly, then the respective advantage of the two can be obtained.
Pressure after detonation reaction zone in high-temperature high-voltage reaction area may be up to 10-30GPa, and temperature is up to 3000-4000 Degree Celsius, it is spread and is grown by vapor reaction, the product grain of synthesis is typically small, usually nanometer grade.Explosive charge shape At shock wave have pressure high, action time is short, the high feature of temperature, synthesizes nano composite oxides using shock wave Object.
Summary of the invention
In order to solve the problems, such as to obtain the uniformly mixed nano composite oxide of height, the present invention provides a kind of explosion sides Formula synthesizes nano composite oxide.The method can produce the nano composite oxides that the height that partial size is 20-100nm is uniformly mixed Object, and simple production process.
The technical solution adopted by the present invention are as follows:
A kind of method of explosive manner synthesis nano composite oxide, includes the following steps:
A, part metals powder is added in explosive, is uniformly mixed;
B, using blower device, make have certain density metallic dust in destructor;
C, mixture is placed in destructor, the volume of device is 53L;
D, primer is collected explosion product, is screened to product.
In the step a expired military explosive be hexogen, TNT etc., metal powder used be iron powder, titanium valve, zinc powder, Copper powder etc..
In the step d, explosion terminates about two ten minutes later, is collected to explosion ash, product is first used to 100 mesh/English The screening of little progress row, then removes moisture removal for 100 DEG C of sample baking oven obtained to obtain dry powder, then use chamber type electric resistance furnace It is heated to 500-1000 DEG C by double crucible method heat treatment in the environment of anaerobic, heating roasting 2-4h.
The resulting nanosize metal oxide of the above method, partial size 20-100nm can be used for making metallic pigments.
Destructor described in the above method is ball-type, and the outer wall of a diameter of 100cm, destructor consist of three layers, Innermost layer is the stainless steel (440-C) of 5mm thickness, also posts the electro-insulating rubber of wiped clean in its inner wall;Centre is 10cm thick Sand;Outermost layer is the stainless steel (154CM) of 2mm thickness.In use, manufactured dedicated composite explosives pack is plugged No. 8 industry Electric cap one is sent out, and is then hung and is fixed at 2/3rds of steel drum height, has reception explosion powder in the bottom of pack Collection device, the top for the spherical tank that explodes is covered using clean rubber skin, then by the door seal for the pillbox that explodes it is good after, utilize Initiator ignites composite explosives pack.About two ten minutes later after reaction, collects the explosion ash being deposited on collecting board.
The innovation of explosive synthesizing nano composite oxides is to be different from conventional chemical method, the conjunction of the approach such as method for constructing At nano material, but the approach for using explosion of " bold " carrys out nano materials, it is characterized in that process is simple, bangs quick-fried When easily generate nanometer spherical particle, can low cost obtain we needs high quality nano composite oxides, existing section Value is ground, also there is very high market value.
Specific embodiment
It is of the invention to further illustrate, it illustrates with the following Examples:
Embodiment 1
A, hexogen and titanium valve are taken respectively, by weight being 6:1, is mixed uniformly, and gross mass is that the blasting charge is made in 5kg
B, using the blower device in destructor, so that the zinc powder concentration in destructor is 35g/L, and disperse equal It is even.
C, the blasting charge is suspended in specific destructor, destructor is ball-type, a diameter of 100cm, explosion dress The outer wall set consists of three layers, and innermost layer is the stainless steel (440-C) of 5mm thickness, also posts the insulation of wiped clean in its inner wall Rubber;Centre is the sand of 10cm thickness;Outermost layer is the stainless steel (154CM) of 2mm thickness.In use, by manufactured dedicated mixing Explosive pack is plugged No. 8 commercial electric detonators one and is sent out, then hung and be fixed at 2/3rds of steel drum height, in pack Bottom have receive explosion powder collection device, the top for the spherical tank that explodes is covered using clean rubber skin, then will be quick-fried After the door seal to blast away a blockhouse is good, composite explosives pack is ignited using initiator.
D, the explosion ash being deposited on collecting board after reaction about two ten minutes later, is collected.Product is first used to 100 mesh/inch It is screened, then removes moisture removal for 100 DEG C of sample baking oven obtained to obtain dry powder, then existed with chamber type electric resistance furnace 550 DEG C are heated to by double crucible method heat treatment in the environment of anaerobic, heating roasting 2h.Our required Gao Pin can be obtained Matter nano composite oxide.
Embodiment 2
A, hexogen, TNT, titanium valve and zinc powder are taken respectively, by weight be 3:3:1:1, gross mass be 4.5kg by its It is uniformly mixed, the blasting charge is made
B, using the blower device in destructor, so that the zinc powder concentration in destructor is 38g/L, titanium valve concentration is 35g/L, and be uniformly dispersed.
C, the blasting charge is suspended in specific destructor, destructor is ball-type, a diameter of 100cm, explosion dress The outer wall set consists of three layers, and innermost layer is the stainless steel (440-C) of 5mm thickness, also posts the insulation of wiped clean in its inner wall Rubber;Centre is the sand of 10cm thickness;Outermost layer is the stainless steel (154CM) of 2mm thickness.In use, by manufactured dedicated mixing Explosive pack is plugged No. 8 commercial electric detonators one and is sent out, then hung and be fixed at 2/3rds of steel drum height, in pack Bottom have receive explosion powder collection device, the top for the spherical tank that explodes is covered using clean rubber skin, then will be quick-fried After the door seal to blast away a blockhouse is good, composite explosives pack is ignited using initiator.
D, the explosion ash being deposited on collecting board after reaction about two ten minutes later, is collected.Product is first used to 100 mesh/inch It is screened, then removes moisture removal for 100 DEG C of sample baking oven obtained to obtain dry powder, then existed with chamber type electric resistance furnace 600 DEG C are heated to by double crucible method heat treatment in the environment of anaerobic, heating roasting 3h.Our required Gao Pin can be obtained Matter nano composite oxide.
Embodiment 3
A, hexogen, TNT, cobalt powder and glass putty are taken respectively, by weight being 5:2:1:1, are mixed uniformly, are made The blasting charge
B, using the blower device in destructor, so that the cobalt powder concentration in destructor is 55g/L, glass putty concentration is 50g/L, and be uniformly dispersed.
C, the blasting charge is suspended in specific destructor, destructor is ball-type, a diameter of 100cm, explosion dress The outer wall set consists of three layers, and innermost layer is the stainless steel (440-C) of 5mm thickness, also posts the insulation of wiped clean in its inner wall Rubber;Centre is the sand of 10cm thickness;Outermost layer is the stainless steel (154CM) of 2mm thickness.In use, by manufactured dedicated mixing Explosive pack is plugged No. 8 commercial electric detonators one and is sent out, then hung and be fixed at 2/3rds of steel drum height, in pack Bottom have receive explosion powder collection device, the top for the spherical tank that explodes is covered using clean rubber skin, then will be quick-fried After the door seal to blast away a blockhouse is good, composite explosives pack is ignited using initiator.
D, the explosion ash being deposited on collecting board after reaction about two ten minutes later, is collected.Product is first used to 100 mesh/inch It is screened, then removes moisture removal for 100 DEG C of sample baking oven obtained to obtain dry powder, then existed with chamber type electric resistance furnace 600 DEG C are heated to by double crucible method heat treatment in the environment of anaerobic, heating roasting 2.5h.It is required high that we can be obtained Quality nano composite oxide.
Embodiment 4
A, hexogen, TNT and glass putty are taken respectively, by weight being 5:3:1, are mixed uniformly, the blasting charge is made
B, using the blower device in destructor, so that the cobalt powder concentration in destructor is 65g/L, and disperse equal It is even.
C, the blasting charge is suspended in specific destructor, destructor is ball-type, a diameter of 100cm, explosion dress The outer wall set consists of three layers, and innermost layer is the stainless steel (440-C) of 5mm thickness, also posts the insulation of wiped clean in its inner wall Rubber;Centre is the sand of 10cm thickness;Outermost layer is the stainless steel (154CM) of 2mm thickness.In use, by manufactured dedicated mixing Explosive pack is plugged No. 8 commercial electric detonators one and is sent out, then hung and be fixed at 2/3rds of steel drum height, in pack Bottom have receive explosion powder collection device, the top for the spherical tank that explodes is covered using clean rubber skin, then will be quick-fried After the door seal to blast away a blockhouse is good, composite explosives pack is ignited using initiator.
D, the explosion ash being deposited on collecting board after reaction about two ten minutes later, is collected.Product is first used to 100 mesh/inch It is screened, then removes moisture removal for 100 DEG C of sample baking oven obtained to obtain dry powder, then existed with chamber type electric resistance furnace 500 DEG C are heated to by double crucible method heat treatment in the environment of anaerobic, heating roasting 3.5h.It is required high that we can be obtained Quality nano composite oxide.
Embodiment described above only describe the preferred embodiments of the invention, not to model of the invention It encloses and is defined, without departing from the spirit of the design of the present invention, this field ordinary engineering and technical personnel is to skill of the invention The various changes and improvements that art scheme is made, should fall within the scope of protection determined by the claims of the present invention.

Claims (4)

1. a kind of explosion method synthesizes nano composite oxide, which comprises the steps of:
A, part metals powder is added in explosive, is uniformly mixed
B, using blower device, make have certain density metallic dust in destructor
C, mixture is placed in destructor, the volume of device is 53L
D, primer is collected explosion product, is screened to product.
2. according to the method described in claim 1, it is characterized by: explosive is hexogen, TNT etc., institute in the step a It is iron powder, titanium valve, zinc powder, copper powder etc. with metal powder.
3. according to the method described in claim 1, it is characterized by: explosion terminates about two ten minutes later, right in the step d Explosion ash is collected, and product is first screened with 100 mesh/inch, then goes to remove water by 100 DEG C of sample baking oven obtained Divide to obtain dry powder, then 500- is heated to by double crucible method heat treatment in the environment of anaerobic with chamber type electric resistance furnace 1000 DEG C, heating roasting 2-4h.
4. being used for the destructor of claim 1 the method, it is characterised in that: the destructor is ball-type, a diameter of The outer wall of 100cm, destructor consist of three layers, and innermost layer is the stainless steel (440-C) of 5mm thickness, also post wiping in its inner wall Clean electro-insulating rubber is wiped, centre is the sand of 10cm thickness, and outermost layer is the stainless steel (154CM) of 2mm thickness;And explosion synthesis dress In setting, there is blower device, it is possible to provide a certain amount of wind-force.
CN201910538103.6A 2019-06-20 2019-06-20 A kind of method of explosive synthesizing nano composite oxides Pending CN110357151A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113943014A (en) * 2021-10-19 2022-01-18 安徽理工大学 Preparation method of zinc-titanium composite metal oxide
CN114507107A (en) * 2022-03-02 2022-05-17 安徽理工大学 Preparation method of special explosive for catalyst doping
BE1029151B1 (en) * 2021-07-27 2022-09-27 Univ Anhui Sci & Technology Process for synthesizing nanoscale lithium iron phosphate battery material by explosion

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1569617A (en) * 2004-05-13 2005-01-26 大连理工大学 Detonation method for synthesizing oxide powder
CN101223412A (en) * 2005-05-11 2008-07-16 奥尔肯工程股份公司 Device for storing, transporting or disposing object
CN109437335A (en) * 2018-11-02 2019-03-08 安徽理工大学 A kind of method of explosion method synthesis NCA battery material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1569617A (en) * 2004-05-13 2005-01-26 大连理工大学 Detonation method for synthesizing oxide powder
CN101223412A (en) * 2005-05-11 2008-07-16 奥尔肯工程股份公司 Device for storing, transporting or disposing object
CN109437335A (en) * 2018-11-02 2019-03-08 安徽理工大学 A kind of method of explosion method synthesis NCA battery material

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
美国金属学会: "《金属手册:粉末冶金》", 30 June 1994 *
郑敏等: ""***法合成纳米α-Fe2O3"", 《硅酸盐学报》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE1029151B1 (en) * 2021-07-27 2022-09-27 Univ Anhui Sci & Technology Process for synthesizing nanoscale lithium iron phosphate battery material by explosion
CN113943014A (en) * 2021-10-19 2022-01-18 安徽理工大学 Preparation method of zinc-titanium composite metal oxide
CN114507107A (en) * 2022-03-02 2022-05-17 安徽理工大学 Preparation method of special explosive for catalyst doping

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