CN109266030A - A kind of preparation method of explosion-suppressing material - Google Patents

A kind of preparation method of explosion-suppressing material Download PDF

Info

Publication number
CN109266030A
CN109266030A CN201810994619.7A CN201810994619A CN109266030A CN 109266030 A CN109266030 A CN 109266030A CN 201810994619 A CN201810994619 A CN 201810994619A CN 109266030 A CN109266030 A CN 109266030A
Authority
CN
China
Prior art keywords
explosion
parts
suppressing material
beaker
preparation
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
CN201810994619.7A
Other languages
Chinese (zh)
Inventor
胡次兵
蒋东明
赵金晶
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.)
Foshan Chancheng No High Environmental Protection Technology Co Ltd
Original Assignee
Foshan Chancheng No High Environmental Protection Technology 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 Foshan Chancheng No High Environmental Protection Technology Co Ltd filed Critical Foshan Chancheng No High Environmental Protection Technology Co Ltd
Priority to CN201810994619.7A priority Critical patent/CN109266030A/en
Publication of CN109266030A publication Critical patent/CN109266030A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K13/00Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
    • C08K13/02Organic and inorganic ingredients
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08HDERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
    • C08H8/00Macromolecular compounds derived from lignocellulosic materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2248Oxides; Hydroxides of metals of copper
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2265Oxides; Hydroxides of metals of iron
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2296Oxides; Hydroxides of metals of zinc

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Materials Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

The present invention relates to a kind of preparation methods of explosion-suppressing material, belong to explosion-suppressing material preparation technical field.First by ammonium sulfate, potassium sulfate and ammonium hydrogen sulfate mixing, and it is impregnated with ethyl orthosilicate and solidliquid mixture is made, dehydrated alcohol is mixed to prepare with solidliquid mixture again and reacts solid, desciccate is made by raw material of bamboo chip, solid will finally be reacted, desciccate and other metal oxide high-temperatures, which are blended, is made explosion-suppressing material, by coated with silica ammonium sulfate, ammonium hydrogen sulfate and potassium sulfate, generate nitrogen, it is improved the stability of ambient enviroment, to inhibit the generation of explosion, maleic anhydride is added in bamboo fibre after separation and acetic anhydride carries out surface and is modified, so that metal ion and bamboo fibre is generated ionic bond and is adsorbed in bamboo fibre surface, reinforce the tightness degree of explosion-suppressing material internal structure, it prevents the embrittlement of explosion-suppressing material and is crushed, it has broad application prospects.

Description

A kind of preparation method of explosion-suppressing material
Technical field
The present invention relates to a kind of preparation methods of explosion-suppressing material, belong to explosion-suppressing material preparation technical field.
Background technique
Recently as the development of national economy, inflammable and explosive liquid (gas) body such as gasoline, liquefied gas, propane is in daily production Using more and more extensive in life.In general, above-mentioned inflammable and explosive liquid (gas) body is stored in fuel tank.Above-mentioned inflammable and explosive The storage of liquid (gas) body and transport field generally use barrier explosion-suppressing material and carry out security hardening to used container, to subtract It is damaged caused by when light generation accidental explosion.
Current explosion-suppressing material is based on aluminum alloy explosion suppression material.The netted explosion-suppressing material of alloy has good heat conductivity, leads The features such as electrical property is strong, large specific surface area, after being sufficiently distributed in fuel tank, can effectively contain flame transmission, make to fire Pressure wave sharp-decay.This netted explosion-suppressing material of alloy surface efficiency with higher in unit volume simultaneously, to have There is good heat absorptivity, the heat absorption that can promptly release burning, the temperature after making combustion reaction reduces, reaction The degrees of expansion of gas reduces, and the pressure value in container increases the limit velocity for less making burning velocity that explosion be not achieved, thus Achieve the purpose that datonation-inhibition.
But the shortcomings that current explosion-suppressing material is that material internal crystallization is big, not closely, hard crisp, without a piece of wood serving as a brake to halt a carriage and extensibility, It is easily broken off, easily falls disintegrating slag.Explosion-suppressing material in fuel tank after a period of use, due to metal meet the corrosive liquids such as soda acid and Easy to oxidize when gas, anticorrosive degree is very poor, and fragment easy to form can fall clast, pollute to oil product when being vibrated Or result in blockage to pipeline road, and be easy to appear collapsing and embrittlement in use, cause container that cannot reach scheduled The capability of antidetonance.
Therefore it provides it is a kind of obstruct quick-fried effect is good, shock resistance and anti-sintering property are strong explosion-suppressing material have it is important Meaning.
Summary of the invention
The technical problems to be solved by the invention, for current explosion-suppressing material poor mechanical property cause easily broken, embrittlement from And fall off and easily form disintegrating slag, while the defect bad for explosion-suppressing material datonation-inhibition function, provide a kind of preparation of explosion-suppressing material Method.
In order to solve the above technical problems, the technical solution adopted by the present invention is that:
A kind of preparation method of explosion-suppressing material, it is characterised in that specific preparation step are as follows:
(1) according to parts by weight, 3~5 parts of ammonium sulfate, 1~2 part of potassium sulfate and 2.5~2.8 parts of ammonium hydrogen phosphate investments are weighed to be blended It is uniformly mixed obtained mixture in machine, the propanedione solution 1:10 in mass ratio of mixture and ethyl orthosilicate is put into beaker In, it is mixed with blender, solidliquid mixture is made;
(2) dehydrated alcohol of solidliquid mixture quality 15~20% is added dropwise into above-mentioned beaker, places the beaker in sonic oscillation instrument Sonic oscillation places the beaker in oil bath pan, heated at constant temperature after oscillation, places the beaker dry in baking oven, obtained reaction Solid, it is spare;
(3) bamboo chip is placed in a beaker, impregnates bamboo chip with sodium hydroxide solution, places the beaker isothermal reaction in water-bath, mistake Filter obtains filter residue, by filter residue 3~5 times wash with distilled water, is put into grinder and grinds, and grinding product is made;
(4) according to parts by weight, 4~6 parts of grinding products, 1.5~1.8 parts of maleic anhydride crystal powders, 1.2~1.5 parts are weighed The ethanol solution that acetic anhydride, 0.4~0.6 part of potassium sulfate and 20~22 parts of mass fractions are 30~40% is put into three-necked flask, is used Blender is mixed, and filter cake is obtained by filtration after stirring, and filter cake is placed in baking oven to dry, obtained desciccate;
(5) according to parts by weight, 1~2 part of above-mentioned desciccate, 0.8~1.2 part of spare reaction product, 3~4 powder oxygen are weighed SiClx, 0.3~0.5 powder iron oxide, 0.2~0.4 part of copper oxide, 1.0~1.3 parts of zinc oxide and 0.3~0.5 part of titanium oxide investment Ground and mixed is uniform in ball mill, puts into high temperature furnace, and under conditions of argon gas protection, datonation-inhibition material is made in high-temperature blending reaction Material.
The mass fraction of the propanedione of ethyl orthosilicate as described in step (1) is 10~15%, and the revolving speed of blender is 500~600r/min, mixing time are 3~5h.
Frequency in sonic oscillation instrument described in step (2) is 30~32kHz, and duration of oscillation is 4~6h, in oil bath pan Oil bath temperature be 160~180 DEG C, the heated at constant temperature time is 100~120min, and the temperature in baking oven is 100~110 DEG C, is done The dry time is 20~22h.
The mass fraction of sodium hydroxide solution described in step (3) is 20~25%, and the bath temperature in water-bath is 90 ~100 DEG C, the isothermal reaction time is 3~4h.
The mass fraction of ethanol solution described in step (4) is 30~40%, and the revolving speed of blender is 400~450r/ Min, mixing time are 50~60min, and the temperature in baking oven is 70~80 DEG C, and drying time is 4~6h.
The high-temperature blending reaction time described in step (5) is 100~110min.
The method have the benefit that:
(1) present invention first mixes ammonium sulfate, potassium sulfate and ammonium hydrogen sulfate, and is impregnated with ethyl orthosilicate and solid-liquid mixing is made Object, then dehydrated alcohol is mixed with solidliquid mixture, it is reacted under high temperature, reaction solid is made after drying, then bamboo chip is placed in alkali Then liquid high temperature boiling is added maleic anhydride, acetic anhydride, potassium sulfate mixing, filters after mixing, is made dry after dry and produces Reaction solid, desciccate and other metal oxide high-temperatures are finally blended and explosion-suppressing material are made by object, and the present invention is by sulfuric acid It is mixed after ammonium, ammonium hydrogen phosphate and potassium sulfate mixing with ethyl orthosilicate, generates silica after dehydrated alcohol is titrated, make dioxy SiClx coats ammonium sulfate, ammonium hydrogen sulfate and potassium sulfate, ammonium sulfate and ammonium hydrogen sulfate and easily decomposes when heated and generate nitrogen, makes surrounding The stability of environment is improved, it is suppressed that the condition of explosion is coated to inhibit the generation of explosion using silica Afterwards, the substances combination degree such as ammonium sulfate, ammonium hydrogen sulfate is improved, thus can be more quickly thermally conductive when heated, be conducive to The decomposition of ammonium ion generates the generation that ammonia inhibits explosion;
(2) bamboo chip is placed in boiling in lye by the present invention, separates the bamboo fibre in bamboo chip, and the bamboo fibre after separation is added Maleic anhydride and acetic anhydride carry out surface and are modified, and so that bamboo fibre surface is introduced a large amount of carboxylic group, to enable bamboo fibre It is reacted with the metal oxide being added later, so that metal ion and bamboo fibre is generated ionic bond, be adsorbed in bamboo fibre surface, Reinforce the tightness degree of explosion-suppressing material internal structure, and inhibit falling off for metal oxide, forms disintegrating slag, prevent explosion-suppressing material Embrittlement and broken, has broad application prospects.
Specific embodiment
According to parts by weight, 3~5 parts of ammonium sulfate, 1~2 part of potassium sulfate and 2.5~2.8 parts of ammonium hydrogen phosphate investments are weighed altogether It is uniformly mixed obtained mixture in mixed machine, mixture is pressed with mass fraction for the propanedione solution of 10~15% ethyl orthosilicates Mass ratio 1:10 is put into beaker, and 3~5h is mixed with the revolving speed of 500~600r/min with blender, solid-liquid mixing is made Object;The dehydrated alcohol of solidliquid mixture quality 15~20% is added dropwise into above-mentioned beaker, places the beaker in sonic oscillation instrument, with 4~6h of ultrasonic frequency oscillation of 30~32kHz places the beaker the oil bath pan that oil bath temperature is 160~180 DEG C after oscillation In, 100~120min of heated at constant temperature is placed the beaker in baking oven, dry 20 under conditions of temperature is 100~110 DEG C~ Reaction solid is made in 22h, spare;Bamboo chip is placed in a beaker, is impregnated with the sodium hydroxide solution that mass fraction is 20~25% Bamboo chip places the beaker in the water-bath that bath temperature is 90~100 DEG C, and filter residue is obtained by filtration in 3~4h of isothermal reaction, will filter It slag 3~5 times wash with distilled water, is put into grinder and grinds, grinding product is made;According to parts by weight, 4~6 parts are weighed to grind Mill product, 1.5~1.8 parts of maleic anhydride crystal powders, 1.2~1.5 parts of acetic anhydrides, 0.4~0.6 part of potassium sulfate and 20~22 parts The ethanol solution that mass fraction is 30~40% is put into three-necked flask, is stirred with blender with the revolving speed mixing of 400~450r/min 50~60min is mixed, filter cake is obtained by filtration after stirring, filter cake is placed in baking oven, dry 4 under conditions of temperature is 70~80 DEG C Desciccate is made in~6h;According to parts by weight, 1~2 part of above-mentioned desciccate is weighed, 0.8~1.2 part of spare reaction produces Object, 3~4 powder silica, 0.3~0.5 powder iron oxide, 0.2~0.4 part of copper oxide, 1.0~1.3 parts of zinc oxide and 0.3~0.5 Ground and mixed is uniform in part titanium oxide investment ball mill, puts into high temperature furnace, under conditions of argon gas protection, high-temperature blending reaction Explosion-suppressing material is made in 100~110min.
Example 1
According to parts by weight, 3 parts of ammonium sulfate, 1 part of potassium sulfate and 2.5 parts of ammonium hydrogen phosphate investment blender and mixings are weighed uniformly to make Mixture is obtained, the propanedione solution 1:10 in mass ratio that mixture and mass fraction are 10% ethyl orthosilicate is put into beaker, 3h is mixed with the revolving speed of 500r/min with blender, solidliquid mixture is made;Solidliquid mixture is added dropwise into above-mentioned beaker The dehydrated alcohol of quality 15% places the beaker in sonic oscillation instrument, will after oscillation with the ultrasonic frequency oscillation 4h of 30kHz Beaker is placed in the oil bath pan that oil bath temperature is 160 DEG C, and heated at constant temperature 100min is placed the beaker in baking oven, is 100 in temperature Reaction solid is made in dry 20h under conditions of DEG C, spare;Bamboo chip is placed in a beaker, the hydroxide for being 20% with mass fraction Sodium solution impregnates bamboo chip, places the beaker in the water-bath that bath temperature is 90 DEG C, and filter residue is obtained by filtration in isothermal reaction 3h, will It filter residue 3 times wash with distilled water, is put into grinder and grinds, grinding product is made;According to parts by weight, 4 parts of grindings are weighed to produce The ethanol solution that object, 1.5 parts of maleic anhydride crystal powders, 1.2 parts of acetic anhydrides, 0.4 part of potassium sulfate and 20 parts of mass fractions are 30% It puts into three-necked flask, 50min is mixed with the revolving speed of 400r/min with blender, filter cake is obtained by filtration after stirring, will filter Cake is placed in baking oven, and desciccate is made in dry 4h under conditions of temperature is 70 DEG C;According to parts by weight, weigh 1 part it is above-mentioned Desciccate, 0.8 part of spare reaction product, 3 powder silica, 0.3 powder iron oxide, 0.2 part of copper oxide, 1.0 parts of zinc oxide and Ground and mixed is uniform in 0.3 part of titanium oxide investment ball mill, puts into high temperature furnace, under conditions of argon gas protection, high-temperature blending It reacts 100min and explosion-suppressing material is made.
Example 2
According to parts by weight, 4 parts of ammonium sulfate, 1 part of potassium sulfate and 2.7 parts of ammonium hydrogen phosphate investment blender and mixings are weighed uniformly to make Mixture is obtained, the propanedione solution 1:10 in mass ratio that mixture and mass fraction are 13% ethyl orthosilicate is put into beaker, 4h is mixed with the revolving speed of 550r/min with blender, solidliquid mixture is made;Solidliquid mixture is added dropwise into above-mentioned beaker The dehydrated alcohol of quality 17% places the beaker in sonic oscillation instrument, will after oscillation with the ultrasonic frequency oscillation 5h of 31kHz Beaker is placed in the oil bath pan that oil bath temperature is 170 DEG C, and heated at constant temperature 110min is placed the beaker in baking oven, is 105 in temperature Reaction solid is made in dry 21h under conditions of DEG C, spare;Bamboo chip is placed in a beaker, the hydroxide for being 23% with mass fraction Sodium solution impregnates bamboo chip, places the beaker in the water-bath that bath temperature is 95 DEG C, and filter residue is obtained by filtration in isothermal reaction 3h, will It filter residue 4 times wash with distilled water, is put into grinder and grinds, grinding product is made;According to parts by weight, 5 parts of grindings are weighed to produce The ethanol solution that object, 1.7 parts of maleic anhydride crystal powders, 1.3 parts of acetic anhydrides, 0.5 part of potassium sulfate and 21 parts of mass fractions are 35% It puts into three-necked flask, 55min is mixed with the revolving speed of 425r/min with blender, filter cake is obtained by filtration after stirring, will filter Cake is placed in baking oven, and desciccate is made in dry 3h under conditions of temperature is 75 DEG C;According to parts by weight, weigh 1 part it is above-mentioned Desciccate, 1.0 parts of spare reaction products, 3 powder silica, 0.4 powder iron oxide, 0.3 part of copper oxide, 1.2 parts of zinc oxide and Ground and mixed is uniform in 0.4 part of titanium oxide investment ball mill, puts into high temperature furnace, under conditions of argon gas protection, high-temperature blending It reacts 105min and explosion-suppressing material is made.
Example 3
According to parts by weight, 5 parts of ammonium sulfate, 2 parts of potassium sulfates and 2.8 parts of ammonium hydrogen phosphate investment blender and mixings are weighed uniformly to make Mixture is obtained, the propanedione solution 1:10 in mass ratio that mixture and mass fraction are 15% ethyl orthosilicate is put into beaker, 5h is mixed with the revolving speed of 600r/min with blender, solidliquid mixture is made;Solidliquid mixture is added dropwise into above-mentioned beaker The dehydrated alcohol of quality 20% places the beaker in sonic oscillation instrument, will after oscillation with the ultrasonic frequency oscillation 6h of 32kHz Beaker is placed in the oil bath pan that oil bath temperature is 180 DEG C, and heated at constant temperature 120min is placed the beaker in baking oven, is 110 in temperature Reaction solid is made in dry 22h under conditions of DEG C, spare;Bamboo chip is placed in a beaker, the hydroxide for being 25% with mass fraction Sodium solution impregnates bamboo chip, places the beaker in the water-bath that bath temperature is 100 DEG C, and filter residue is obtained by filtration in isothermal reaction 4h, will It filter residue 5 times wash with distilled water, is put into grinder and grinds, grinding product is made;According to parts by weight, 6 parts of grindings are weighed to produce The ethanol solution that object, 1.8 parts of maleic anhydride crystal powders, 1.5 parts of acetic anhydrides, 0.6 part of potassium sulfate and 22 parts of mass fractions are 40% It puts into three-necked flask, 60min is mixed with the revolving speed of 450r/min with blender, filter cake is obtained by filtration after stirring, will filter Cake is placed in baking oven, and desciccate is made in dry 6h under conditions of temperature is 80 DEG C;According to parts by weight, weigh 2 parts it is above-mentioned Desciccate, 1.2 parts of spare reaction products, 4 powder silica, 0.5 powder iron oxide, 0.4 part of copper oxide, 1.3 parts of zinc oxide and Ground and mixed is uniform in 0.5 part of titanium oxide investment ball mill, puts into high temperature furnace, under conditions of argon gas protection, high-temperature blending It reacts 110min and explosion-suppressing material is made.
Comparative example
With the explosion-suppressing material of company of Harbin City production as a comparison case in explosion-suppressing material produced by the present invention and comparative example Explosion-suppressing material detected, testing result is as shown in table 1:
Tensile strength test
It is detected by the regulation of GB/T10120-2013.
Datonation-inhibition function test
The explosion-suppressing material in explosion-suppressing material produced by the present invention and comparative example is added in methane respectively and carries out methane explosion in fact It tests.
1 performance measurement result of table
Test item Example 1 Example 2 Example 3 Comparative example
Tensile strength (MPa) 265 274 281 182
Yield strength (MPa) 101 105 109 78
Fatigue strength (MPa) 65 68 70 48
Elongation percentage (%) 40.1 41.8 42.6 33.8
Datonation-inhibition property Blast pressure is small, explosion Sensitive period, is long, boosting speed Rate is slow Blast pressure is small, explosion Sensitive period, is long, boosting speed Rate is slow Blast pressure is small, quick-fried Fried sensitive period, is long, rises Press rate slow Sensitive period of exploding, is short, rises Press rate fast
According to data in table 1 it is found that explosion-suppressing material produced by the present invention, has good anti-extrusion, collapse, without scaling-off and strong High datonation-inhibition function is spent, and simple process is easy, extends the service life of explosion-suppressing material, have broad prospects.

Claims (6)

1. a kind of preparation method of explosion-suppressing material, it is characterised in that specific preparation step are as follows:
(1) according to parts by weight, 3~5 parts of ammonium sulfate, 1~2 part of potassium sulfate and 2.5~2.8 parts of ammonium hydrogen phosphate investments are weighed to be blended It is uniformly mixed obtained mixture in machine, the propanedione solution 1:10 in mass ratio of mixture and ethyl orthosilicate is put into beaker In, it is mixed with blender, solidliquid mixture is made;
(2) dehydrated alcohol of solidliquid mixture quality 15~20% is added dropwise into above-mentioned beaker, places the beaker in sonic oscillation instrument Sonic oscillation places the beaker in oil bath pan, heated at constant temperature after oscillation, places the beaker dry in baking oven, obtained reaction Solid, it is spare;
(3) bamboo chip is placed in a beaker, impregnates bamboo chip with sodium hydroxide solution, places the beaker isothermal reaction in water-bath, mistake Filter obtains filter residue, by filter residue 3~5 times wash with distilled water, is put into grinder and grinds, and grinding product is made;
(4) according to parts by weight, 4~6 parts of grinding products, 1.5~1.8 parts of maleic anhydride crystal powders, 1.2~1.5 parts are weighed The ethanol solution that acetic anhydride, 0.4~0.6 part of potassium sulfate and 20~22 parts of mass fractions are 30~40% is put into three-necked flask, is used Blender is mixed, and filter cake is obtained by filtration after stirring, and filter cake is placed in baking oven to dry, obtained desciccate;
(5) according to parts by weight, 1~2 part of above-mentioned desciccate, 0.8~1.2 part of spare reaction product, 3~4 powder oxygen are weighed SiClx, 0.3~0.5 powder iron oxide, 0.2~0.4 part of copper oxide, 1.0~1.3 parts of zinc oxide and 0.3~0.5 part of titanium oxide investment Ground and mixed is uniform in ball mill, puts into high temperature furnace, and under conditions of argon gas protection, datonation-inhibition material is made in high-temperature blending reaction Material.
2. a kind of preparation method of explosion-suppressing material according to claim 1, it is characterised in that: it is as described in step (1) just The mass fraction of the propanedione of silester is 10~15%, and the revolving speed of blender is 500~600r/min, mixing time For 3~5h.
3. a kind of preparation method of explosion-suppressing material according to claim 1, it is characterised in that: surpass described in step (2) Frequency in sound oscillation instrument is 30~32kHz, and duration of oscillation is 4~6h, and the oil bath temperature in oil bath pan is 160~180 DEG C, permanent Warm heating time is 100~120min, and the temperature in baking oven is 100~110 DEG C, and drying time is 20~22h.
4. a kind of preparation method of explosion-suppressing material according to claim 1, it is characterised in that: hydrogen described in step (3) The mass fraction of sodium hydroxide solution is 20~25%, and the bath temperature in water-bath is 90~100 DEG C, the isothermal reaction time is 3~ 4h。
5. a kind of preparation method of explosion-suppressing material according to claim 1, it is characterised in that: second described in step (4) The mass fraction of alcoholic solution is 30~40%, and the revolving speed of blender is 400~450r/min, mixing time is 50~ 60min, the temperature in baking oven are 70~80 DEG C, and drying time is 4~6h.
6. a kind of preparation method of explosion-suppressing material according to claim 1, it is characterised in that: height described in step (5) The warm blending reaction time is 100~110min.
CN201810994619.7A 2018-08-29 2018-08-29 A kind of preparation method of explosion-suppressing material Pending CN109266030A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810994619.7A CN109266030A (en) 2018-08-29 2018-08-29 A kind of preparation method of explosion-suppressing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810994619.7A CN109266030A (en) 2018-08-29 2018-08-29 A kind of preparation method of explosion-suppressing material

Publications (1)

Publication Number Publication Date
CN109266030A true CN109266030A (en) 2019-01-25

Family

ID=65155010

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810994619.7A Pending CN109266030A (en) 2018-08-29 2018-08-29 A kind of preparation method of explosion-suppressing material

Country Status (1)

Country Link
CN (1) CN109266030A (en)

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102634703A (en) * 2012-05-08 2012-08-15 王季庄 Explosion-suppressing material and preparation method thereof
CN102634704A (en) * 2012-05-08 2012-08-15 王季庄 Noncorrosive compression-resisting explosion-suppressing material and preparation method thereof
CN103301787A (en) * 2013-07-03 2013-09-18 陕西盟创纳米新型材料股份有限公司 Silicon dioxide aerogel composite material and molding method
CN104276366A (en) * 2014-09-30 2015-01-14 深圳国能合创能源技术有限公司 Corrosion-resistant and abrasion-resistant explosion suppression material and preparation method thereof
CN107310875A (en) * 2017-06-28 2017-11-03 常州汉唐文化传媒有限公司 A kind of Nonmetal barrier explosion-proof material and preparation method thereof
CN107365927A (en) * 2017-06-30 2017-11-21 常州创索新材料科技有限公司 A kind of explosion-suppressing material and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102634703A (en) * 2012-05-08 2012-08-15 王季庄 Explosion-suppressing material and preparation method thereof
CN102634704A (en) * 2012-05-08 2012-08-15 王季庄 Noncorrosive compression-resisting explosion-suppressing material and preparation method thereof
CN103301787A (en) * 2013-07-03 2013-09-18 陕西盟创纳米新型材料股份有限公司 Silicon dioxide aerogel composite material and molding method
CN104276366A (en) * 2014-09-30 2015-01-14 深圳国能合创能源技术有限公司 Corrosion-resistant and abrasion-resistant explosion suppression material and preparation method thereof
CN107310875A (en) * 2017-06-28 2017-11-03 常州汉唐文化传媒有限公司 A kind of Nonmetal barrier explosion-proof material and preparation method thereof
CN107365927A (en) * 2017-06-30 2017-11-21 常州创索新材料科技有限公司 A kind of explosion-suppressing material and preparation method thereof

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
《日用搪瓷生产基本知识》编写组编: "《日用搪瓷生产基本知识》", 31 May 1982, 轻工业出版社 *
云南省化学石油工业厅技术情报中心站编: "《云南省化工产品手册 增订本》", 30 April 1986 *
周文英等著: "《聚合物基导热复合材料》", 30 June 2017, 国防工业出版社 *
李永祥等: ""硝酸铵的降感技术研究"", 《含能材料》 *
江体乾主编: "《化工工艺手册》", 29 February 1992, 上海科学技术出版社 *
王戈等著: "《竹纤维性能及其纺织加工应用》", 31 March 2017, 中国纺织出版社 *
秦浩正主编: "《中学生学习辞典.化学卷》", 30 September 2012, 上海世界图书出版公司 *
邢晓江等: ""管内粉尘抑爆效果的实验研究"", 《弹道学报》 *

Similar Documents

Publication Publication Date Title
CN102205962B (en) Device and method for preparing activated carbon material for electrochemical capacitor
Wei et al. Suppression effects of ABC powder on explosion characteristics of hybrid C2H4/polyethylene dust
CN104316429B (en) The method of test alkali metal and zinc fume STRENGTH ON COKE destruction and performance impact
CN105903146A (en) Novel ultrafine dry powder extinguishing agent and preparation method
CN109266030A (en) A kind of preparation method of explosion-suppressing material
Sun et al. Co-gasification characteristics of coke blended with hydro-char and pyro-char from bamboo
CN105779076B (en) A kind of preparation method of efficient fuel coal desulfurizing agent
CN104711044B (en) A kind of alcohol-based fuel and preparation method thereof
CN108329955A (en) A kind of processing method of energy-efficient green liquid fuel
CN106064816B (en) A kind of rotary alkali activation prepares the device and method of activated carbon
CN102173714B (en) Environment-friendly calcium silicate heat insulation product and preparation method thereof
CN101144043A (en) Environmental protection high-energy mixed light hydrocarbon industrial gas and producing method thereof
CN107400500A (en) A kind of preparation method of complex intensifying shot
CN107189832A (en) A kind of preparation method of water Jiao slurry
CN113322112A (en) High-calorific-value composite biomass granular fuel and preparation method thereof
Han et al. Characterization and kinetics of iron oxide reduction by corn straw biochar prepared by pyrolysis using superheated steam atmosphere and hydrothermal processes
CN106362345A (en) Preparation method for aerosol fire-extinguishing agent
CN106868482A (en) A kind of passivating method of nickel magnesium alloy
CN109054883A (en) A kind of preparation method of Bio-fuel-oil
CN100365107C (en) Easy ignited, stable burning synthetic liquid fuel in high heat value, and preparation method
CN108130140A (en) A kind of preparation method of high-energy corrosion resistant type biodiesel
CN104888800B (en) A kind of preparation method of the Pd/carbon catalyst of composition metal
CN109554199A (en) A kind of technique based on biomass fuel processing saturated vapor
Sirun et al. Effect of Density and Hardness on Burning Rate of Water Hyacinth and Coconut Shell Briquettes
Li et al. The Application of Microwave Pyrolysis Pilot Equipment: the Craft of Gas-Carbon Co-production from Rice Straw Particles

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20190125

WD01 Invention patent application deemed withdrawn after publication