CN113755095A - Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof - Google Patents

Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof Download PDF

Info

Publication number
CN113755095A
CN113755095A CN202110853903.4A CN202110853903A CN113755095A CN 113755095 A CN113755095 A CN 113755095A CN 202110853903 A CN202110853903 A CN 202110853903A CN 113755095 A CN113755095 A CN 113755095A
Authority
CN
China
Prior art keywords
powder
parts
nano
hydrophobic
mixing
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.)
Granted
Application number
CN202110853903.4A
Other languages
Chinese (zh)
Other versions
CN113755095B (en
Inventor
孙俊荣
蒋玉广
冯亚凯
王伟志
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.)
Zhongbin Tianke (Tianjin) High-tech Co.,Ltd.
Zhongbin Tianke Tianjin New Material Co ltd
Original Assignee
Zhongbin Tianke Tianjin New Material Co ltd
Zhongbin Tianke Xinyang New Material 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 Zhongbin Tianke Tianjin New Material Co ltd, Zhongbin Tianke Xinyang New Material Co ltd filed Critical Zhongbin Tianke Tianjin New Material Co ltd
Priority to CN202110853903.4A priority Critical patent/CN113755095B/en
Publication of CN113755095A publication Critical patent/CN113755095A/en
Application granted granted Critical
Publication of CN113755095B publication Critical patent/CN113755095B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D183/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
    • C09D183/04Polysiloxanes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/70Additives characterised by shape, e.g. fibres, flakes or microspheres
    • 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
    • C08K2003/2217Oxides; Hydroxides of metals of magnesium
    • C08K2003/222Magnesia, i.e. magnesium oxide
    • 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
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium
    • 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
    • C08K2003/2262Oxides; Hydroxides of metals of manganese
    • 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
    • C08K2003/2272Ferric oxide (Fe2O3)

Abstract

The invention provides nano antifreezing anti-cracking hydrophobic blue crystal powder, which is prepared from the following raw materials: the coating comprises the following components of cyanite powder, scale-shaped natural mica powder, organosilane emulsion, nano hydrophobic fumed silica, sodium methyl silicate, magnesium aluminum silicate, a surface modifier, a dispersing agent and calcium lignosulfonate. The blue crystal powder forms a fine concave-convex structure on the surface of concrete to form a lotus leaf hydrophobic effect, and improves the water resistance, the water impermeability, the crack resistance and the weather resistance of the concrete, thereby comprehensively improving the durability of the concrete structure and prolonging the service life.

Description

Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof
Technical Field
The invention belongs to the field of hydrophobic blue crystal powder preparation, and particularly relates to nano anti-freezing anti-cracking hydrophobic blue crystal powder and a preparation method thereof.
Background
Concrete waterproof materials are mainly classified into flexible waterproof and rigid waterproof. Flexible waterproofing refers to the wrapping of a structure with waterproofing rolls or waterproofing paint. The rigid waterproof is to rely on the compactness of the structural member or adopt rigid materials as waterproof layers to achieve the waterproof purpose of buildings, namely to improve the impermeability of concrete.
At present, flexible waterproof is mostly adopted in China, the service life of the flexible waterproof structure is within 15 years, the flexible waterproof structure does not meet the regulation of general waterproof standards of building and municipal engineering, and the self compactness of the structural part cannot meet the requirement of the impermeability grade of most buildings.
Therefore, the waterproof agent for improving the waterproof and anti-permeability grade of the concrete has great market demand, most rigid materials improve the anti-permeability performance of the concrete in terms of self-healing and compactness, and the prior art can influence or reduce other performance indexes of the concrete while improving a certain performance index of the concrete, indirectly influence the durability of the concrete, and rarely gives consideration to the multifunctional rigid waterproof material for comprehensively improving the durability of the concrete.
Based on the nano antifreezing anti-cracking hydrophobic blue crystal powder and the preparation method thereof, the waterproof impermeability, the crack resistance and the weather resistance of the concrete are improved, so that the durability of the concrete structure is comprehensively improved, and the service life is prolonged.
Disclosure of Invention
In order to solve the technical problems, the invention provides nano anti-freezing anti-cracking hydrophobic blue crystal powder which is prepared from the following raw materials in parts by weight: 100-120 parts of cyanite powder, 120 parts of scale-shaped natural mica powder, 40-60 parts of organosilane emulsion, 30-50 parts of nano hydrophobic fumed silica, 3-5 parts of sodium methyl silicate, 1-3 parts of magnesium aluminum silicate, 0.1-0.3 part of surface modifier, 0.1-0.3 part of dispersant and 0.2-0.3 part of calcium lignosulfonate.
Preferably, the cyanite powder is one of fibrous cyanite powder and platy cyanite powder.
Preferably, the mica powder comprises the following chemical components: SiO 22:36-45%,Al2O3:10-17%,MgO:19-27%, K2O:7-12%,Fe2O3:3-7%,MnO2:1-3%,TiO2:0.3-0.5%,H2O:4-6%。
Preferably, the organosilane emulsion is a hydroxyl group and ether group modified silicone emulsion.
Preferably, the surface modifier is cetyltrimethylammonium bromide.
Preferably, the dispersant is sodium tripolyphosphate.
Preferably, the preparation method comprises the following steps:
step 1: mineral separation and crushing: mixing the sapphire powder and the scaly natural mica powder in parts by weight, putting the mixture into a grinder to grind the mixture into powder of 300-400 meshes, and standing the powder for later use;
step 2: mixing materials: sequentially adding the dispersant, sodium methyl silicate and nano hydrophobic fumed silica in parts by weight into the organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding the magnesium aluminum silicate and the surface modifier in parts by weight, heating to 50-70 ℃ and maintaining for 0.5-2h, then adding the mixture obtained in the step (2), heating to 70-90 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until the liquid is completely evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained product and grinding to 300-400 meshes;
and 5: vapor-phase active deposition: and introducing compressed gas into the obtained product, depositing, cooling, adding the lignin calcium sulfonate, and fully mixing for 15-30min to improve powder flowability.
Preferably, the speed of the high-speed stirring and mixing in the step 2 is 1000-.
Preferably, the stirring speed of the high-speed stirring reaction kettle in the step 3 is 400-800 rpm.
Compared with the prior art, the invention has the beneficial effects that:
1. the prepared blue crystal powder is a hydrophobic material, the microcosmic lower-layer laminated sheet and the flaky palace' association network of the magnesium aluminum silicate play roles in blocking and nano-scale fiber traction, the tension of the inner surface of concrete is increased, the inner space of the blue crystal powder is V-shaped, a hydration heat diffusion channel is relieved, and the problems of temperature fission, drying shrinkage fission, freeze thawing and reinforcing steel bar corrosion cracking caused by temperature change, water loss and water infiltration are reduced.
2. The blue crystal powder forms a fine concave-convex structure on the surface of concrete, forms a lotus leaf hydrophobic effect, and improves the water resistance, the water impermeability, the crack resistance and the weather resistance of the concrete, thereby comprehensively improving the durability of the concrete structure and prolonging the service life.
Detailed Description
The invention is further described:
example 1:
100 parts of cyanite powder, 110 parts of scale-like natural mica powder, 50 parts of organosilane emulsion, 40 parts of nano hydrophobic fumed silica, 3 parts of sodium methylsilicate, 3 parts of magnesium aluminum silicate, 0.3 part of surface modifier, 0.2 part of dispersant and 0.2 part of calcium lignosulfonate.
Specifically, the preparation method of the nanometer anti-freezing anti-cracking hydrophobic blue crystal powder comprises the following steps:
step 1: mineral separation and crushing: mixing 100 parts of cyanite powder and 110 parts of scaly natural mica powder, and grinding into 375-mesh powder;
step 2: mixing materials: sequentially adding 0.2 part of dispersing agent, 3 parts of sodium methyl silicate and 40 parts of nano hydrophobic fumed silica into 50 parts of organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding 3 parts of magnesium aluminum silicate and 0.3 part of surface modifier, heating to 50-60 ℃ for maintaining for 0.5h, adding the mixture obtained in the step (2), heating to 70-80 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until all liquid is evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained product and grinding the dried product to 375 meshes;
and 5: vapor-phase active deposition: and introducing compressed gas into the obtained product, depositing, cooling, adding the lignin calcium sulfonate, fully mixing for 15min, and improving the powder flowability.
Example 2:
120 parts of cyanite powder, 100 parts of scale-like natural mica powder, 60 parts of organosilane emulsion, 40 parts of nano hydrophobic fumed silica, 3 parts of sodium methylsilicate, 3 parts of magnesium aluminum silicate, 0.3 part of surface modifier, 0.2 part of dispersant and 0.2 part of calcium lignosulfonate.
Specifically, the preparation method of the nanometer anti-freezing anti-cracking hydrophobic blue crystal powder comprises the following steps:
step 1: mineral separation and crushing: mixing 120 parts of cyanite powder and 100 parts of scaly natural mica powder, and grinding into 400-mesh powder;
step 2: mixing materials: sequentially adding 0.2 part of dispersing agent, 3 parts of sodium methyl silicate and 40 parts of nano hydrophobic fumed silica into 60 parts of organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding 3 parts of aluminum-magnesium silicate and 0.3 part of surface modifier, heating to 50-60 ℃ for maintaining for 0.5h, adding the mixture obtained in the step (2), heating to 80-90 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until all liquid is evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained product and grinding to 400 meshes;
and 5: and introducing compressed gas into the obtained product, depositing, cooling, adding calcium lignosulfonate, and fully mixing for 15min to improve powder flowability.
Example 3:
120 parts of cyanite powder, 110 parts of scale-like natural mica powder, 50 parts of organosilane emulsion, 50 parts of nano hydrophobic fumed silica, 2 parts of sodium methylsilicate, 2 parts of magnesium aluminum silicate, 0.3 part of surface modifier, 0.3 part of dispersant and 0.2 part of calcium lignosulfonate.
Specifically, the preparation method of the nanometer anti-freezing anti-cracking hydrophobic blue crystal powder comprises the following steps:
step 1: mineral separation and crushing: mixing 120 parts of cyanite powder and 110 parts of scaly natural mica powder, and grinding into 400-mesh powder;
step 2: mixing materials: sequentially adding 0.3 part of dispersing agent, 2 parts of sodium methyl silicate and 50 parts of nano hydrophobic fumed silica into 50 parts of organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding 2 parts of aluminum-magnesium silicate and 0.3 part of surface modifier, heating to 50-60 ℃ for 1 hour, adding the mixture obtained in the step (2), heating to 80-90 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until the liquid is completely evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained product and grinding the dried product to 400 meshes;
and 5: vapor-phase active deposition: and introducing compressed gas into the obtained product, depositing, cooling, adding calcium lignosulfonate, and fully mixing for 20min to improve powder flowability.
Example 4:
100 parts of cyanite powder, 100 parts of scale-like natural mica powder, 60 parts of organosilane emulsion, 40 parts of nano hydrophobic fumed silica, 3 parts of sodium methylsilicate, 3 parts of magnesium aluminum silicate, 0.3 part of surface modifier, 0.3 part of dispersant and 0.2 part of calcium lignosulfonate.
Specifically, the preparation method of the nanometer anti-freezing anti-cracking hydrophobic blue crystal powder comprises the following steps:
step 1: mineral separation and crushing: mixing 100 parts of cyanite powder and 100 parts of scaly natural mica powder, and grinding into 400-mesh powder;
step 2: mixing materials: sequentially adding 0.3 part of dispersing agent, 3 parts of sodium methyl silicate and 40 parts of nano hydrophobic fumed silica into 60 parts of organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding 3 parts of aluminum-magnesium silicate and 0.3 part of surface modifier, heating to 50-60 ℃ for maintaining for 0.5h, adding the mixture obtained in the step (2), heating to 80-90 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until all liquid is evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained product and grinding the dried product to 400 meshes;
and 5: vapor-phase active deposition: and introducing compressed gas into the obtained product, depositing, cooling, adding calcium lignosulfonate, and fully mixing for 20min to improve powder flowability.
Example 5:
100 parts of cyanite powder, 120 parts of scale-shaped natural mica powder, 50 parts of organosilane emulsion, 3 parts of nano hydrophobic fumed silica, 3 parts of sodium methyl silicate, 3 parts of magnesium aluminum silicate, 0.3 part of surface modifier, 0.3 part of dispersant and 0.3 part of calcium lignosulfonate.
Specifically, the preparation method of the nanometer anti-freezing anti-cracking hydrophobic blue crystal powder comprises the following steps:
step 1: mineral separation and crushing: mixing 100 parts of cyanite powder and 120 parts of scaly natural mica powder, and grinding into 400-mesh powder;
step 2: mixing materials: sequentially adding 0.3 part of dispersing agent, 3 parts of sodium methyl silicate and 50 parts of nano hydrophobic fumed silica into 50 parts of organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding 3 parts of aluminum-magnesium silicate and 0.3 part of surface modifier, heating to 50-60 ℃ for 1.5h, adding the mixture obtained in the step (2), heating to 80-90 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until all liquid is evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained materials and grinding the dried materials to 400 meshes;
and 5: vapor-phase active deposition: and introducing compressed gas into the obtained product, depositing, cooling, adding calcium lignosulfonate, and fully mixing for 20min to improve powder flowability.
Application example:
the anti-freezing anti-cracking hydrophobic blue crystal powder with 2 percent of nano is added, and the following performance tests are carried out according to the national standard GB/T50082-2009 test of the long-term performance and durability of common concrete according to the same concrete material mixing ratio:
water barrier properties (deep water height method): 3d, 28 d; impervious height ratio: 56.3 percent and 31.2 percent.
Freeze-thaw resistance (tested by a rapid freeze-thaw method, the mass loss of a concrete test piece is not more than 5 percent, and the dynamic elastic modulus is not less than 60 percent): 528 times.
Shrinkage ratio (3 d): 104 percent.
Compressive strength ratio: 3d and 28d are 110% and 108%, respectively.
Early crack resistance ratio: 79.8 percent, after the surface of the test piece is smeared for 30min, the test piece is blown by wind for 60min, and the running water is sprayed for maintenance.
Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the appended claims and their equivalents.

Claims (9)

1. The nanometer anti-freezing anti-cracking hydrophobic blue crystal powder is characterized by being prepared from the following raw materials in parts by weight: 100-120 parts of cyanite powder, 120 parts of scaly natural mica powder, 40-60 parts of organosilane emulsion, 30-50 parts of nano hydrophobic fumed silica, 3-5 parts of sodium methylsilicate, 1-3 parts of magnesium aluminum silicate, 0.1-0.3 part of surface modifier, 0.1-0.3 part of dispersant and 0.2-0.3 part of calcium lignosulfonate.
2. The nano antifreezing anti-cracking hydrophobic cyanite powder as claimed in claim 1, wherein the cyanite powder is one of fibrous cyanite powder and platy cyanite powder.
3. The nano anti-freezing anti-cracking hydrophobic blue crystal powder as claimed in claim 1, wherein the chemical components of the mica powder are as follows: SiO 22:36-45%,Al2O3:10-17%,MgO:19-27%,K2O:7-12%,Fe2O3:3-7%,MnO2:1-3%,TiO2:0.3-0.5%,H2O:4-6%。
4. The nano antifreeze anti-crack hydrophobic blue crystal powder as claimed in claim 1, wherein the organosilane emulsion is a hydroxyl group and ether group modified organosilicon emulsion.
5. The nano antifreeze anti-crack hydrophobic blue crystal powder as claimed in claim 1, wherein the surface modifier is cetyl trimethyl ammonium bromide.
6. The nano antifreeze anti-crack hydrophobic blue crystal powder as claimed in claim 1, wherein the dispersant is sodium tripolyphosphate.
7. The preparation method of the nano anti-freezing anti-cracking hydrophobic blue crystal powder as claimed in claim 1, characterized by comprising the following steps:
step 1: mineral separation and crushing: mixing the sapphire powder and the scaly natural mica powder in parts by weight, putting the mixture into a grinder to grind the mixture into powder of 300-400 meshes, and standing the powder for later use;
step 2: mixing materials: sequentially adding the dispersant, sodium methyl silicate and nano hydrophobic fumed silica in parts by weight into the organosilane emulsion, and stirring and mixing at a high speed to fully infiltrate and disperse the organosilane emulsion and the nano hydrophobic fumed silica to form a mixture;
and step 3: and (3) physicochemical reaction: adding the powder obtained in the step (1) into a high-speed stirring reaction kettle, sequentially adding the magnesium aluminum silicate and the surface modifier in parts by weight, heating to 50-70 ℃ for maintaining for 0.5-2h, adding the mixture obtained in the step (2), heating to 70-90 ℃, fully mixing, reacting in the high-speed stirring reaction kettle until the liquid is completely evaporated, and fully wrapping the powder with the mixture to obtain a product;
and 4, step 4: drying and grinding: drying the obtained product and grinding to 300-400 meshes;
and 5: vapor-phase active deposition: introducing compressed gas into the obtained product, depositing, cooling, adding calcium lignosulfonate, mixing for 15-30min, and improving powder fluidity.
8. The method as claimed in claim 7, wherein the mixing speed in step 2 is 1500 rpm/min.
9. The method as claimed in claim 7, wherein the stirring speed of the high-speed stirring reaction kettle in step 3 is 400-800 rpm.
CN202110853903.4A 2021-07-28 2021-07-28 Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof Active CN113755095B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110853903.4A CN113755095B (en) 2021-07-28 2021-07-28 Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110853903.4A CN113755095B (en) 2021-07-28 2021-07-28 Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof

Publications (2)

Publication Number Publication Date
CN113755095A true CN113755095A (en) 2021-12-07
CN113755095B CN113755095B (en) 2022-05-24

Family

ID=78788011

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110853903.4A Active CN113755095B (en) 2021-07-28 2021-07-28 Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof

Country Status (1)

Country Link
CN (1) CN113755095B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115536303A (en) * 2022-08-26 2022-12-30 华能莱芜发电有限公司 Concrete internal-doped anti-permeability hydrophobic material, preparation method and application

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102190467A (en) * 2011-05-23 2011-09-21 西南科技大学 Anti-seepage and anti-crack dry-mixed mortar
CN103332903A (en) * 2013-05-31 2013-10-02 成都新柯力化工科技有限公司 Self-crystallized polymer cement-based waterproof coating, and preparation method thereof
CN105174798A (en) * 2015-09-16 2015-12-23 桂林市和鑫防水装饰材料有限公司 Inorganic silicon-organic silicon composite infiltration crystalline type concrete waterproofer
JP2016176004A (en) * 2015-03-20 2016-10-06 横浜ゴム株式会社 Two-liquid room temperature curing type urethane coating film waterproof material composition
CN109535860A (en) * 2018-11-15 2019-03-29 成都新柯力化工科技有限公司 A kind of organic-inorganic nano water-repellent paint and preparation method
CN112830742A (en) * 2021-01-29 2021-05-25 烟台华宝新材料科技有限公司 High-impermeability concrete and preparation method thereof

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102190467A (en) * 2011-05-23 2011-09-21 西南科技大学 Anti-seepage and anti-crack dry-mixed mortar
CN103332903A (en) * 2013-05-31 2013-10-02 成都新柯力化工科技有限公司 Self-crystallized polymer cement-based waterproof coating, and preparation method thereof
JP2016176004A (en) * 2015-03-20 2016-10-06 横浜ゴム株式会社 Two-liquid room temperature curing type urethane coating film waterproof material composition
CN105174798A (en) * 2015-09-16 2015-12-23 桂林市和鑫防水装饰材料有限公司 Inorganic silicon-organic silicon composite infiltration crystalline type concrete waterproofer
CN109535860A (en) * 2018-11-15 2019-03-29 成都新柯力化工科技有限公司 A kind of organic-inorganic nano water-repellent paint and preparation method
CN112830742A (en) * 2021-01-29 2021-05-25 烟台华宝新材料科技有限公司 High-impermeability concrete and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
张宇震编著: "《中国铝酸盐水泥生产与应用》", 31 January 2014, 中国建材工业出版社 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115536303A (en) * 2022-08-26 2022-12-30 华能莱芜发电有限公司 Concrete internal-doped anti-permeability hydrophobic material, preparation method and application
CN115536303B (en) * 2022-08-26 2023-11-03 华能莱芜发电有限公司 Concrete internal doped impervious hydrophobic material, preparation method and application

Also Published As

Publication number Publication date
CN113755095B (en) 2022-05-24

Similar Documents

Publication Publication Date Title
CN110627383B (en) Preparation method of transparent fireproof gel and composite fireproof glass
CN113755095B (en) Nanometer anti-freezing anti-cracking hydrophobic blue crystal powder and preparation method thereof
CN102898917A (en) Reflection and heat insulation paint for buildings
CN101914329A (en) Nano multifunctional outer wall heat preservation coating
CN109232850A (en) A kind of fire-retardant low thermal conductivity rigid polyurethane foam of aeroge modified heat resistant and preparation method thereof
CN112680003A (en) Inorganic heat-insulating coating and preparation method thereof
CN113087460A (en) Environment-friendly anti-freezing concrete and preparation method thereof
CN107652722A (en) A kind of composite coating material of silicone-modified Ludox and preparation method thereof
CN112551993A (en) Anti-freezing concrete
CN111363421A (en) Fluorine-silicon nano waterproof heat-insulation composite material and preparation method thereof
CN101914331A (en) Montmorillonite-based nano composite heat insulation coating
CN111348883A (en) Autoclaved aerated concrete with high crack resistance and low water absorption rate and preparation method thereof
CN113480267A (en) High-performance concrete applying machine-made sand and preparation method thereof
CN110054917A (en) A kind of inorganic heat preservation coating composition, inorganic heat preservation coating
CN113185237A (en) Nano-enhanced phase-change antifreezing concrete mixture and preparation method thereof
CN113831088B (en) Phase-change large-volume concrete and preparation method thereof
CN114105531A (en) Method for producing high-performance concrete by utilizing solid wastes
CN114436582A (en) Underwater non-dispersible ultrahigh-performance concrete and preparation method thereof
CN115594999B (en) Breathable mineral coating special for ultralow VOC concrete and preparation method thereof
CN112724749A (en) Reflective heat-insulation composite coating and preparation method thereof
CN110511638B (en) Functional heat-insulating environment-friendly coating material and preparation method thereof
CN112456878A (en) Novel CO2High-temperature corrosion-resistant well cementation cement system for-EGS-mode hot dry rock
CN110734686A (en) waterborne reflective heat-insulating coating and preparation method thereof
CN114702290B (en) Thermal-insulation energy-saving environment-friendly mortar and preparation method thereof
CN112126284B (en) Waterproof heat-insulating coating for external wall and preparation method thereof

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
GR01 Patent grant
GR01 Patent grant
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20220921

Address after: A107-1, Binhai Times Building, No. 590 Huzhou Road, Binhai-Zhongguancun Science and Technology Park, Economic and Technological Development Zone, Binhai New Area, Tianjin 300457

Patentee after: Zhongbin Tianke (Tianjin) High-tech Co.,Ltd.

Patentee after: Zhongbin Tianke (Tianjin) new material Co.,Ltd.

Address before: 464000 100m east of Gongshi Road, high tech Industrial Park, Xinyang City, Henan Province

Patentee before: Zhongbin Tianke (Xinyang) new material Co.,Ltd.

Patentee before: Zhongbin Tianke (Tianjin) new material Co.,Ltd.