CN106565197B - A kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation - Google Patents
A kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation Download PDFInfo
- Publication number
- CN106565197B CN106565197B CN201610914632.8A CN201610914632A CN106565197B CN 106565197 B CN106565197 B CN 106565197B CN 201610914632 A CN201610914632 A CN 201610914632A CN 106565197 B CN106565197 B CN 106565197B
- Authority
- CN
- China
- Prior art keywords
- flyash
- airsetting
- barrier material
- heat preservation
- gel
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B30/00—Compositions for artificial stone, not containing binders
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/02—Treatment
- C04B20/023—Chemical treatment
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2201/00—Mortars, concrete or artificial stone characterised by specific physical values
- C04B2201/30—Mortars, concrete or artificial stone characterised by specific physical values for heat transfer properties such as thermal insulation values, e.g. R-values
- C04B2201/32—Mortars, concrete or artificial stone characterised by specific physical values for heat transfer properties such as thermal insulation values, e.g. R-values for the thermal conductivity, e.g. K-factors
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Processing Of Solid Wastes (AREA)
- Silicon Compounds (AREA)
Abstract
The present invention provides a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation, it is reacted first using flyash with industrial waste acid, to flyash surface preparation, foreign ion is dissolved into industrial waste acid, using high-temperature roasting repeatedly and basification, fine coal gray surface is subjected to gelation, and then connect the main body of flyash, it is connected with each other between powder, forms network skeleton structure, then reacted by constant pressure and dry and obtain aerosil.The present invention is not only at low cost, and flyash gelatinizing-in-situ, and obtained heat preserving and insulating material micropore is evenly distributed, and intensity is big.While solving environmental pollution, more turn waste into wealth, improves the utility value of flyash.
Description
Technical field
The present invention relates to functional material preparation fields, and in particular to a kind of building heat preservation of flyash airsetting gelatinization preparation every
Hot material.
Background technique
Aeroge is solid most light in the world, it is one kind using three-dimensional net structure as bracket, wherein filling gas
Decentralized medium has porous condensed state matter.Aerogel material has large specific surface area, porosity height, the coefficient of heat conduction
Low, the advantages that density is low, doping adsorption capacity is strong, in the energy, information, environmental protection, medicine, pesticide, metallurgy, catalysis and basic section
The fields such as research are learned all to have broad application prospects.The main component of aeroge is earth silicon material, and prepares titanium dioxide
The silicon source that silica aerogel uses is usually ethyl orthosilicate, polyethoxy disiloxane, methyltrimethoxysilane, silicon tetrachloride
Equal organo-silicon compound, these compounds are expensive.Since the main component of flyash is silica, there is invention special at present
Benefit is to use flyash as silicon source, significantly reduces the production cost of aeroge in this way.
Chinese invention patent application number 201110445784.5 discloses a kind of flyash and composite diatomite preparation SiO2
Airsetting gluing method, which prepares the medium temperature mechanical activation of flyash and diatomite, silicon dioxide gel, prepared by wet gel,
Mother liquor aging, six step exchange of solvent surface modification, constant pressure and dry steps, obtained SiO2Aeroge with using waterglass as silicon
The aerogel material similar performance in source, because using flyash and composite diatomite as cheap silicon source and constant pressure and dry technique,
So that production cost is greatly lowered, widely answered so that having in fields such as construction material, insulation, environmental-protection adsorptions
Use prospect.However, contain the impurity elements such as iron, copper in the aeroge of preparation due to, there are a large amount of impurity, will lead in flyash,
Reduce the heat-insulating property of material.
Chinese invention patent application number 200910010685.7 discloses a kind of using flyash while preparing SiO2Airsetting
The method of glue and zeolite.Flyash is first carried out high-temperature activation processing by this method, then carries out hydro-thermal conjunction with sodium hydrate aqueous solution
At reaction, waterglass is catalyzed with certain density sulfuric acid, or by solution carry out cation exchange resin exchange after again
Base catalysis processing is carried out, SiO is obtained2Gel, with alcohols/alkane solvents and trim,ethylchlorosilane mixed solution to hydrogel into
After row solvent replacement/surface modification treatment, SiO is obtained under the conditions of constant pressure and dry2Aeroge.The invention is not only solid waste
One new way of the high-effect recycling of object, and be also SiO2One new technique of aeroge and the preparation of zeolite low cost
Method.But in the invention it is also the composition without paying attention to flyash, for the aeroge of preparation there are impurity, heat insulation is uneven
It is even.
According to above-mentioned analysis, at present using during coal ash for manufacturing prepared silicon dioxide aeroge, not to flyash into
The corresponding purification process of row, most of is to obtain silica dioxide gel after directly reacting flyash with alkali, then pass through normal pressure
Dry to obtain aerosil, the impurity content that will lead in aerosil in this way is high, leads to the heat-insulated effect of material
Fruit is uneven.So needing a kind of side purifying flyash, the method that side obtains silica dioxide gel in situ at present.
Summary of the invention
During using coal ash for manufacturing prepared silicon dioxide aeroge at present, flyash is carried out corresponding pure
Change processing, most of is to obtain silica dioxide gel after directly reacting flyash with alkali, then obtains two by constant pressure and dry
Silica aerogel, the impurity content that will lead in aerosil in this way is high, causes material heat insulation uneven.This
Invention proposes a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation, anti-using flyash and industrial waste acid first
It answers, to flyash surface preparation, foreign ion is dissolved into industrial waste acid, at high-temperature roasting repeatedly and alkalization
Reason, obtains the flyash of surface gelling, and the main body of flyash still has, and mutually accumulates, and forms skeleton structure, then leads to
It crosses constant pressure and dry reaction and obtains aerosil.The present invention is not only at low cost, and flyash gelatinizing-in-situ, obtains
Heat preserving and insulating material micropore is evenly distributed, and intensity is big.While solving environmental pollution, more turn waste into wealth, improves flyash
Utility value.
The present invention provides a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation, using flyash as former
Material, using alternately alkalization-heating method, the control reaction time obtains silica dioxide gel, and the specific method is as follows:
(1) flyash is added in industrial waste acid, the temperature that industrial waste acid is arranged is 30-80 DEG C, mixing speed 100-
Under conditions of 500 revs/min, its pH value is adjusted between 3-4, carries out flyash surface preparation, using pre- place is obtained by filtration
The mass ratio of the flyash powder of reason, the flyash and industrial waste acid is 0.2-20:1;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, and temperature setting is 300-800 DEG C,
The calcination activation time is set as 10-90 minutes, and ball mill mechanical lapping is passed through after the completion of roasting, obtains activating fly ash;
(3) by activating fly ash in proportion at 70-100 DEG C with aqueous slkali hybrid reaction, the reaction time is that 0.5-6 is small
When, mixture is filtered after reaction, carries out rapid dilution to filter residue with excessive water, the silicon and aqueous slkali of fine coal gray surface are anti-
It answers, gelation occurs, obtain the flyash of surface gelling, the concentration of the aqueous slkali is 0.05-0.2mol/L;
(4) step (2) and (3) are repeated 2-5 times, purifies the silica dioxide gel of fine coal gray surface, obtain surface purifying powder
Coal ash gel solution is again heated to 60-70 DEG C, and water-reducing agent is added, stirs evenly, obtains flyash gel, then by the powder
Coal ash gel, which is added in alcoholic solvent, to react 5-10 hours, then pulls out and be put into drying box, dry 13- at being 60-70 DEG C in temperature
20 hours, obtain flyash aeroge, the mass ratio of the water-reducing agent and the flyash gel is 1:100-1000.
Preferably, the flyash is appointing in level-one flyash, second class powered coal ash, three-level flyash and superfined flyash
It anticipates one kind.
Preferably, the industrial waste acid is one or more of Waste Sulfuric Acid, waste nitric acid, waste hydrochloric acid.
Preferably, the high-temperature roasting is sintered using vacuum Muffle furnace, and the air pressure of 100-1000Pa is kept in sintering process.
Preferably, the ball mill mechanical lapping uses hardened steel ball, stainless steel ball, tungsten-carbide ball, zirconia ceramics ball
Any one of, Ball-milling Time is 2-6 hours.
Preferably, the aqueous slkali is any one of ammonium hydroxide, sodium hydroxide, ammonium fluoride or two or more combinations;
The alcoholic solvent is any one of methanol, ethyl alcohol, isopropanol, normal propyl alcohol or two or more combinations.
Preferably, the water-reducing agent is lignosulfonates, naphthalene sulphonate formaldehyde polymer, sulfamate, powder gather
Any one in carboxylate, poly carboxylic acid series water reducer.
The present invention proposes a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation, compared with prior art,
Prominent feature and excellent effect are:
1, the present invention uses industrial waste acid treated coal ash, removes the impurity of fine coal gray surface, ensure that later period preparation two
The homogeneity of ingredients of silica aerogel, micropore size homogeneity.
2, the present invention makes flyash while retaining own form using high-temperature roasting and surface basification repeatedly,
Gelation occurs for surface, obtains the skeleton and packing material of aeroge in situ.
3, the present invention uses constant pressure and dry technique, instead of aeroge prepare in the high cost supercritical drying skill that generallys use
Art significantly reduces the production cost of aerogel material, provides scale and streaming production model.
4, the flyash and industrial waste acid that the present invention uses prepare aerosil as raw material, put into small, acyclic
Border pollution can significantly reduce cost, have significant market application value.
Specific embodiment
In the following, the present invention will be further described in detail by way of specific embodiments, but this should not be interpreted as to the present invention
Range be only limitted to example below.Without departing from the idea of the above method of the present invention, according to ordinary skill
The various replacements or change that knowledge and customary means are made, should be included in the scope of the present invention.
Embodiment 1
(1) level-one flyash is added in industrial waste sulfuric acid, the temperature that industrial waste sulfuric acid is arranged is 30 DEG C, and mixing speed is
Under conditions of 100 revs/min, its pH value is adjusted between 3-4, carries out the surface preparation of level-one flyash, using being obtained by filtration
The mass ratio of pretreated flyash powder, level-one flyash and industrial waste sulfuric acid is 1:5;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, is sintered using vacuum Muffle furnace,
100 air pressure is kept in sintering process, temperature setting is 300 DEG C, and the calcination activation time is set as 10 minutes, and roasting passes through after completing
Ball mill mechanical lapping is crossed, ball mill mechanical lapping can use hardened steel ball, and Ball-milling Time is 2 hours, obtain activation fine coal
Ash;
(3) by activating fly ash in proportion at 70 DEG C with aqueous slkali hybrid reaction, the reaction time is 0.5 hour, reaction
Mixture is filtered afterwards, carries out rapid dilution to filter residue with excessive water, the silicon and concentration of fine coal gray surface are 0.05mol/L's
Ammonium hydroxide reaction, occurs gelation, obtains the flyash of surface gelling;Activating fly ash is with alkali sodium hydroxide solution mass ratio
1:1.5;
(4) step (2) and (3) 2 times are repeated, the silica dioxide gel of fine coal gray surface is purified, obtain surface purifying fine coal
Grey gel solution is again heated to 60 DEG C, and water-reducing agent sodium lignin sulfonate is added, stirs evenly, obtains flyash gel, then will
The flyash gel, which is added in alcoholic solvent, to react 5 hours, then pulls out and be put into drying box, and dry 13 is small at being 60 DEG C in temperature
When, obtain flyash aeroge, the mass ratio of sodium lignin sulfonate and flyash gel is 1:100.
By the building heat preservation heat-barrier material for the flyash airsetting gelatinization preparation that method in embodiment 1 is prepared, by property
It is as shown in table 1 that energy test obtains parameter.
Embodiment 2
(1) second class powered coal ash is added in Industry Waste hydrochloric acid, the temperature of setting Industry Waste hydrochloric acid is 40 DEG C, and mixing speed is
Under conditions of 200 revs/min, its pH value is adjusted between 3-4, carries out flyash surface preparation, using pre- place is obtained by filtration
The mass ratio of the flyash powder of reason, flyash and industrial waste sulfuric acid is 1:1;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, is sintered using vacuum Muffle furnace,
The air pressure of 300Pa is kept in sintering process, temperature setting is 400 DEG C, and the calcination activation time is set as 30 minutes, after the completion of roasting
By ball mill mechanical lapping, ball mill mechanical lapping can use stainless steel ball, and Ball-milling Time is 3 hours, obtain activation powder
Coal ash;
(3) by activating fly ash in proportion at 80 DEG C with alkali sodium hydroxide solution hybrid reaction, the reaction time is 1.5 small
When, mixture is filtered after reaction, carries out rapid dilution to filter residue with excessive water, silicon and the concentration of fine coal gray surface are
The alkali sodium hydroxide solution of 0.15mol/L reacts, and gelation occurs, obtains the flyash of surface gelling;Activating fly ash with
Alkali sodium hydroxide solution mass ratio is 1:1;
(4) step (2) and (3) 3 times are repeated, the silica dioxide gel of fine coal gray surface is purified, obtain surface purifying fine coal
Grey gel solution is again heated to 65 DEG C, and water-reducing agent sulfamic acid sodium is added, stirs evenly, obtains flyash gel, then by institute
It states flyash gel and is added in ethyl alcohol and react 6 hours, then pull out and be put into drying box, it is 13 hours dry at being 60 DEG C in temperature,
Obtain flyash aeroge, the mass ratio of sulfamic acid sodium and flyash gel is 1:200.
By the building heat preservation heat-barrier material for the flyash airsetting gelatinization preparation that method in embodiment 2 is prepared, by property
It is as shown in table 1 that energy test obtains parameter.
Embodiment 3
(1) superfined flyash is added in industrial waste nitric acid, the temperature that waste nitric acid is arranged is 60 DEG C, mixing speed 300
Under conditions of rev/min, its pH value is adjusted between 3-4, progress flyash surface preparation is pretreated using being obtained by filtration
The mass ratio of flyash powder, flyash and waste nitric acid is 5:1;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, is sintered using vacuum Muffle furnace,
The air pressure of 500Pa is kept in sintering process, temperature setting is 500 DEG C, and the calcination activation time is set as 50 minutes, after the completion of roasting
By ball mill mechanical lapping, ball mill mechanical lapping can use tungsten-carbide ball, and Ball-milling Time is 4 hours, obtain activation powder
Coal ash;
(3) by activating fly ash in proportion at 90 DEG C with ammonium fluoride solution hybrid reaction, the reaction time is 3 hours, instead
Mixture is filtered after answering, and carries out rapid dilution to filter residue with excessive water, the silicon and concentration of fine coal gray surface are 0.17mol/L
Ammonium fluoride solution reaction, occur gelation, obtain the flyash of surface gelling;Activating fly ash and alkali sodium hydroxide solution
Mass ratio is 3:1;
(4) step (2) and (3) 3 times are repeated, the silica dioxide gel of fine coal gray surface is purified, obtain surface purifying fine coal
Grey gel solution is again heated to 65 DEG C, and powder polycarboxylate is added, stirs evenly, obtains flyash gel, then by the powder
Coal ash gel, which is added in isopropanol, to react 8 hours, then pulls out and be put into drying box, 15 hours dry at being 65 DEG C in temperature, obtains
To flyash aeroge, the mass ratio of powder polycarboxylate and flyash gel is 1:500.
By the building heat preservation heat-barrier material for the flyash airsetting gelatinization preparation that method in embodiment 3 is prepared, by property
It is as shown in table 1 that energy test obtains parameter.
Embodiment 4
(1) three-level flyash is added in industrial waste nitric acid, setting waste nitric acid is 70 with the temperature of waste hydrochloric acid mixing spent acid
DEG C, under conditions of mixing speed is 400 revs/min, its pH value is adjusted between 3-4, carries out flyash surface preparation, using
It is obtained by filtration pretreated flyash powder, the mass ratio of flyash and waste nitric acid is 10:1;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, is sintered using vacuum Muffle furnace,
The air pressure of 800Pa is kept in sintering process, temperature setting is 700 DEG C, and the calcination activation time is set as 80 minutes, after the completion of roasting
By ball mill mechanical lapping, ball mill mechanical lapping can use zirconia ceramics ball, and Ball-milling Time is 5 hours, be lived
Change flyash;
(3) by activating fly ash in proportion at 90 DEG C with ammonium fluoride and ammonium hydroxide mixed solution hybrid reaction, reaction time
It is 5 hours, mixture is filtered after reaction, carries out rapid dilution, the silicon and concentration of fine coal gray surface to filter residue with excessive water
It is reacted for the ammonium fluoride solution of 0.18mol/L, gelation occurs, obtains the flyash of surface gelling;Activating fly ash and fluorine
Change ammonium and ammonium hydroxide mixed solution solution quality ratio is 5:1;
(4) step (2) and (3) 4 times are repeated, the silica dioxide gel of fine coal gray surface is purified, obtain surface purifying fine coal
Grey gel solution is again heated to 65 DEG C, and naphthalene sulphonate formaldehyde polymer is added, stirs evenly, obtains flyash gel, then will
The flyash gel, which is added in isopropanol and normal propyl alcohol mixed liquor, to react 9 hours, then pulls out and be put into drying box, is in temperature
It is 18 hours dry at 65 DEG C, flyash aeroge is obtained, naphthalene sulphonate formaldehyde polymer and the mass ratio of flyash gel are 1:
800。
By the building heat preservation heat-barrier material for the flyash airsetting gelatinization preparation that method in embodiment 4 is prepared, by property
It is as shown in table 1 that energy test obtains parameter.
Embodiment 5
(1) by three-level flyash addition industrial waste sulfuric acid, waste nitric acid, waste hydrochloric acid mixed liquor, setting Waste Sulfuric Acid, give up nitre
Acid, waste hydrochloric acid mixing spent acid temperature be 80 DEG C, under conditions of mixing speed is 500 revs/min, adjust its pH value between 3-4,
Flyash surface preparation is carried out, using pretreated flyash powder, the mass ratio of flyash and waste nitric acid is obtained by filtration
For 20:1;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, is sintered using vacuum Muffle furnace,
The air pressure of 1000Pa is kept in sintering process, temperature setting is 800 DEG C, and the calcination activation time is set as 90 minutes, and roasting is completed
Afterwards by ball mill mechanical lapping, ball mill mechanical lapping uses zirconia ceramics ball, and Ball-milling Time is 6 hours, is activated
Flyash;
(3) by activating fly ash in proportion at 90 DEG C with ammonium fluoride, sodium hydroxide and ammonium hydroxide mixed solution hybrid reaction,
Reaction time is 6 hours, and mixture is filtered after reaction, carries out rapid dilution to filter residue with excessive water, fine coal gray surface
Silicon is reacted with the ammonium fluoride solution that concentration is 0.2mol/L, and gelation occurs, obtains the flyash of surface gelling;Activate fine coal
Ash is 5:1 with ammonium fluoride, sodium hydroxide and ammonium hydroxide mixed solution solution quality ratio;
(4) step (2) and (3) 4 times are repeated, the silica dioxide gel of fine coal gray surface is purified, obtain surface purifying fine coal
Grey gel solution is again heated to 70 DEG C, and naphthalene sulphonate formaldehyde polymer is added, stirs evenly, obtains flyash gel, then will
The flyash gel, which is added in isopropanol and normal propyl alcohol mixed liquor, to react 10 hours, then pulls out and be put into drying box, in temperature
It is drying 20 hours at 70 DEG C, obtains flyash aeroge, naphthalene sulphonate formaldehyde polymer and the mass ratio of flyash gel are
1:1000。
By the building heat preservation heat-barrier material for the flyash airsetting gelatinization preparation that method in embodiment 5 is prepared, by property
It is as shown in table 1 that energy test obtains parameter.
Table 1
Performance indicator | Porosity ml/g | Porosity % | 100 DEG C of thermal coefficient W/m K | 700 DEG C of thermal coefficient W/m K |
Embodiment 1 | 3.2 | 90 | 0.012 | 0.042 |
Embodiment 2 | 2.9 | 89 | 0.016 | 0.055 |
Embodiment 3 | 3.3 | 92 | 0.013 | 0.052 |
Embodiment 4 | 3.1 | 91 | 0.014 | 0.062 |
Embodiment 5 | 3.3 | 90 | 0.017 | 0.072 |
Claims (7)
1. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation, it is characterised in that using flyash as raw material,
Using alternately alkalization-heating method, the control reaction time obtains silica dioxide gel, and the specific method is as follows:
(1) flyash is added in industrial waste acid, the temperature that industrial waste acid is arranged is 30-80 DEG C, mixing speed 100-500
Under conditions of rev/min, its pH value is adjusted between 3-4, progress flyash surface preparation is pretreated using being obtained by filtration
The mass ratio of flyash powder, the flyash and industrial waste acid is 0.2-20:1;
(2) the pretreated flyash powder for obtaining step (1) passes through high-temperature roasting, and temperature setting is 300-800 DEG C, roasting
Activation time is set as 10-90 minutes, and ball mill mechanical lapping is passed through after the completion of roasting, obtains activating fly ash;
(3) by activating fly ash in proportion at 70-100 DEG C with aqueous slkali hybrid reaction, the reaction time is 0.5-6 hours, instead
Mixture is filtered after answering, and carries out rapid dilution to filter residue with excessive water, and the silicon of fine coal gray surface is reacted with aqueous slkali, is occurred
Gelation, obtains the flyash of surface gelling, and the concentration of the aqueous slkali is 0.05-0.2mol/L;
(4) step (2) and (3) are repeated 2-5 times, purifies the silica dioxide gel of fine coal gray surface, obtain surface purifying flyash
Gel solution is again heated to 60-70 DEG C, and water-reducing agent is added, stirs evenly, obtains flyash gel, then by the flyash
Gel, which is added in alcoholic solvent, to react 5-10 hours, then pulls out and be put into drying box, and dry 13-20 is small at being 60-70 DEG C in temperature
When, obtain flyash aeroge, the mass ratio of the water-reducing agent and the flyash gel is 1:100-1000.
2. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation according to claim 1, it is characterised in that: institute
Stating flyash is any one in level-one flyash, second class powered coal ash, three-level flyash and superfined flyash.
3. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation according to claim 1, it is characterised in that: institute
Stating industrial waste acid is one or more of Waste Sulfuric Acid, waste nitric acid, waste hydrochloric acid.
4. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation according to claim 1, it is characterised in that: institute
It states high-temperature roasting to be sintered using vacuum Muffle furnace, the air pressure of 100-1000Pa is kept in sintering process.
5. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation according to claim 1, it is characterised in that: institute
Ball mill mechanical lapping is stated using any one of hardened steel ball, stainless steel ball, tungsten-carbide ball, zirconia ceramics ball, when ball milling
Between be 2-6 hours.
6. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation according to claim 1, it is characterised in that: institute
Stating aqueous slkali is any one of ammonium hydroxide, sodium hydroxide, ammonium fluoride or two or more combinations;
The alcoholic solvent is any one of methanol, ethyl alcohol, isopropanol, normal propyl alcohol or two or more combinations.
7. a kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation according to claim 1, it is characterised in that: institute
Water-reducing agent is stated to subtract for lignosulfonates, naphthalene sulphonate formaldehyde polymer, sulfamate, powder polycarboxylate, polycarboxylic-acid
Any one in aqua.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610914632.8A CN106565197B (en) | 2016-10-20 | 2016-10-20 | A kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610914632.8A CN106565197B (en) | 2016-10-20 | 2016-10-20 | A kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106565197A CN106565197A (en) | 2017-04-19 |
CN106565197B true CN106565197B (en) | 2019-01-18 |
Family
ID=58533192
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610914632.8A Expired - Fee Related CN106565197B (en) | 2016-10-20 | 2016-10-20 | A kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN106565197B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109210319A (en) * | 2018-11-12 | 2019-01-15 | 中研信源(北京)节能科技有限公司 | A kind of aerogel vacuum thermal insulation plate and its core material with and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101538046A (en) * | 2009-03-10 | 2009-09-23 | 大连工业大学 | Method for simultaneously preparing SiO2 aerogel and zeolite by utilizing fly ash |
WO2010129200A4 (en) * | 2009-04-27 | 2010-12-29 | Rockwool International A/S | Aerogel compositions and methods of making and using them |
CN104961135A (en) * | 2015-07-01 | 2015-10-07 | 卓达新材料科技集团有限公司 | Preparation method of silicon dioxide aerogel |
EP2931677A1 (en) * | 2012-12-11 | 2015-10-21 | EMPA Eidgenössische Materialprüfungs- und Forschungsanstalt | Thermally insulating aerogel based rendering materials |
-
2016
- 2016-10-20 CN CN201610914632.8A patent/CN106565197B/en not_active Expired - Fee Related
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101538046A (en) * | 2009-03-10 | 2009-09-23 | 大连工业大学 | Method for simultaneously preparing SiO2 aerogel and zeolite by utilizing fly ash |
WO2010129200A4 (en) * | 2009-04-27 | 2010-12-29 | Rockwool International A/S | Aerogel compositions and methods of making and using them |
EP2931677A1 (en) * | 2012-12-11 | 2015-10-21 | EMPA Eidgenössische Materialprüfungs- und Forschungsanstalt | Thermally insulating aerogel based rendering materials |
CN104961135A (en) * | 2015-07-01 | 2015-10-07 | 卓达新材料科技集团有限公司 | Preparation method of silicon dioxide aerogel |
Non-Patent Citations (1)
Title |
---|
常压干燥制备SiO2气凝胶及其结构、性能研究;史非;《中国博士学位论文全文数据库 工程科技Ⅰ辑》;20080315(第3期);B020-52 |
Also Published As
Publication number | Publication date |
---|---|
CN106565197A (en) | 2017-04-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101717214B (en) | Method for preparing silicon-aluminum aerogel by using fly ash as raw material through normal pressure drying | |
CN110040743A (en) | A kind of coal ash for manufacturing for SSZ-13 molecular sieve method | |
CN109569545B (en) | Method for preparing aluminum-silicon porous material from fly ash | |
CN107640777A (en) | A kind of method for preparing big/mesoporous zeolite molecular sieve of crystal seed induction | |
CN108911599B (en) | Method for simultaneously preparing iron oxide and silicon dioxide aerogel pad from iron tailings | |
CN107083097A (en) | A kind of indoor putty capable of purifying air and preparation method | |
CN109354029B (en) | Method for preparing mesoporous silicon oxide from fly ash | |
CN105664841A (en) | Hydration-calcination modification method of high-temperature CO2 adsorption material Li4SiO4 | |
CN103769045B (en) | A kind of preparation method of fly ash base high-performance adsorbing material | |
CN103539147A (en) | Preparation method of silicon dioxide molecular sieve | |
CN111848212A (en) | Preparation method of porous ceramic material for adjusting humidity | |
CN107376835B (en) | Efficient hydrogen production adsorbent and preparation method thereof | |
CN108658130A (en) | A method of preparing iron oxide and aerosil simultaneously from iron tailings | |
CN106565197B (en) | A kind of building heat preservation heat-barrier material of flyash airsetting gelatinization preparation | |
CN114904479A (en) | Preparation of CO from coal-fired solid waste fly ash 2 Method for producing adsorbent | |
CN108249456A (en) | A kind of method that grade hole Y type molecular sieve is prepared using rice husk as raw material | |
CN101474514B (en) | Method for preparing modified ultra-high molecular mass polyethylene micropore filter element | |
CN109174044B (en) | Method for improving specific surface area and adsorption capacity of opal | |
CN113845128A (en) | MOR zeolite molecular sieve and preparation method thereof | |
CN104528788A (en) | Method for preparing porous aluminum oxide aerogel | |
CN115849389B (en) | Method for rapidly preparing silicon dioxide aerogel powder by mixed solvent system | |
CN109665534A (en) | A method of mesopore silicon oxide is prepared using flyash acid leaching residue | |
CN108929072B (en) | Method for preparing ferric oxide and nano composite heat insulation material from iron tailings | |
CN112939492B (en) | Preparation method of coal gangue geopolymer | |
CN114132937A (en) | Preparation method of large-block silicon dioxide aerogel |
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 | ||
TA01 | Transfer of patent application right | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20181130 Address after: 756000 Salt Chemical Industrial Park, Guyuan Economic Development Zone, Ningxia Hui Autonomous Region Applicant after: GUYUAN KAIYUAN ENERGY SAVING BUILDING MATERIAL CO., LTD. Address before: 610091 Donghai Road, Jiao long industrial port, Qingyang District, Chengdu, Sichuan 4 Applicant before: Chengdu Xinkeli Chemical Sci-Tech Co., Ltd. |
|
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20190118 Termination date: 20191020 |