CN113788687B - Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair - Google Patents

Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair Download PDF

Info

Publication number
CN113788687B
CN113788687B CN202110937005.7A CN202110937005A CN113788687B CN 113788687 B CN113788687 B CN 113788687B CN 202110937005 A CN202110937005 A CN 202110937005A CN 113788687 B CN113788687 B CN 113788687B
Authority
CN
China
Prior art keywords
spray coating
minutes
aluminum
mixture
resistant spray
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.)
Active
Application number
CN202110937005.7A
Other languages
Chinese (zh)
Other versions
CN113788687A (en
Inventor
陈金凤
程水明
丛培源
项冰
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
China First Metallurgical Group Co Ltd
Wuhan Research Institute of Metallurgical Construction Co Ltd
Original Assignee
China First Metallurgical Group Co Ltd
Wuhan Research Institute of Metallurgical Construction Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by China First Metallurgical Group Co Ltd, Wuhan Research Institute of Metallurgical Construction Co Ltd filed Critical China First Metallurgical Group Co Ltd
Priority to CN202110937005.7A priority Critical patent/CN113788687B/en
Publication of CN113788687A publication Critical patent/CN113788687A/en
Application granted granted Critical
Publication of CN113788687B publication Critical patent/CN113788687B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/66Monolithic refractories or refractory mortars, including those whether or not containing clay
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/62204Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products using waste materials or refuse
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3418Silicon oxide, silicic acids, or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3427Silicates other than clay, e.g. water glass
    • C04B2235/3463Alumino-silicates other than clay, e.g. mullite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/349Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/44Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
    • C04B2235/447Phosphates or phosphites, e.g. orthophosphate, hypophosphite
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/50Constituents or additives of the starting mixture chosen for their shape or used because of their shape or their physical appearance
    • C04B2235/52Constituents or additives characterised by their shapes
    • C04B2235/5208Fibers
    • C04B2235/5216Inorganic
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/74Physical characteristics
    • C04B2235/77Density
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P40/00Technologies relating to the processing of minerals
    • Y02P40/60Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes

Abstract

The invention discloses a preparation method of an aluminum-silicon wear-resistant spray coating for hot repair, which comprises the steps of adding waste electric ceramic particles and silica fume into a planetary type mixing machine according to the mass ratio of 100: 20-25, and mixing for 5-8 minutes to obtain a mixed particle material; adding the obtained mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary mixing machine to mix for 10-12 minutes to obtain a precursor mixture; sequentially adding chrysotile fibers accounting for 6-8 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 8-10 wt% of the precursor mixture into the precursor mixture, stirring for 5-8 minutes, and sealing for ageing for 30-40 minutes to obtain a mixture; adding carboxymethyl cellulose accounting for 0.5-1.5 wt% of the mixture into the obtained mixture, and stirring for 5-8 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair; the obtained wear-resistant spray coating has the advantages of strong associativity, good sintering integrity with a lining body, less construction resilience, strong wear resistance and simple preparation process, takes industrial solid wastes as raw materials, greatly reduces the development cost of the spray coating, and is environment-friendly.

Description

Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair
Technical Field
The invention belongs to the technical field of coatings, and particularly relates to a preparation method of an aluminum-silicon wear-resistant spray coating for thermal state repair
Background
The spray coating is an unshaped refractory material which is constructed by taking high-speed airflow as a carrier, is mainly suitable for quickly repairing the lining of a kiln, does not need to erect a template in the construction process, and has the characteristics of time saving, labor saving and quick construction.
The spray coating can be classified into dry spraying, semi-wet spraying, mixed spraying and the like, but generally, the spray coating is required to have good bonding property, adhesiveness and sintering property (weibo. "influence of binder variety on spray repair material performance", refractory and lime ", 2019, 44 (6): pp 35-37).
The binding property of the spray paint mainly derives from the performance of a binding agent, and the currently commonly used binding agent comprises water system binding (Zhang Qingxia, Nie Jianhua, Lihong wave, and the like) which mainly comprises cement, water glass or sol and the like 2 Influence of fine powder on performance of cement-bonded aluminum-magnesium gunning material "[ refractory ], 2020, 54 (5): pp 390-394), the binding agents have the following disadvantages: (1) the water system combined spray paint inevitably contains a large amount of water, which is beneficial to construction, but finally escapes at high temperature to leave air holes in the material, so that the material is cracked; (2) the high temperature performance of water-based bonded spray coatings is degraded by the impurity components in the binder. For example, the cement contains calcium, the water glass contains sodium and the like, and the components are easy to form low-melting-point phases at high temperature, so that the high-temperature performance of the spray paint is seriously influenced.
The adhesion of the spray paint is mainly due to the interaction of the grain composition of the components with the binder. Too high or too low adhesion is not good for spray coating (Rong. "development of plastic gunning method and gunning material", fire-resistant and lime, 2011, 36 (1): pp 26-29). The adhesion is too high, and the spray paint is easy to agglomerate and difficult to spread; too low adhesiveness leads to more rebound of the spray paint, waste of raw materials and influence on construction.
The sintering performance of the spray coating is mainly reflected in two aspects, namely the spray coating can be rapidly sintered, and can also be sintered with a body material of a kiln lining body to form an effective whole (the influence of a magnesium oxide raw material on the sintering performance of the electric furnace gunning material; refractories and limes, 2017, 42 (4): pp 30-33). Therefore, the sintering performance of the gunning material itself cannot be measured, and the gunning material and the lining body are considered to form sintering and be tightly combined under the service environment.
CN201910783154.5 discloses a thermal state repairing spray coating and a preparation method thereof, which is prepared by taking brown corundum, Guangxi mud and pure calcium aluminate cement as main raw materials and adding water for mixing; although the problem of rapid hot repair is solved, the spray paint has good bonding and high strength; however, the cement in combination with the calcium-containing component deteriorates the high temperature thermal state properties of the spray paint.
CN201310366807.2 discloses a gunning mix for kiln repair, which is prepared by taking magnesite, forsterite and the like as main raw materials and borax as a bonding agent, adding water and mixing uniformly; although the adhesion rate of the gunning material is improved, the anti-stripping performance is good; however, magnesite and other raw materials are high in cost and easy to hydrate, and the hardening and sintering of the materials are affected.
CN201610010144.4 discloses an andalusite corundum falling-resistant gunning mix, which takes andalusite corundum as a raw material and is tightly combined by embedding and wrapping andalusite and corundum; although the refractory degree, the thermal shock resistance and the falling prevention of the gunning material are improved; however, the mismatch of the thermal expansion coefficients of the raw material components at high temperature easily causes microcracks and pores in the material.
Disclosure of Invention
The invention mainly aims to provide a preparation method of an aluminum-silicon wear-resistant spray coating for thermal state repair, which has the advantages of strong binding property, good sintering integrity with a lining body, less construction resilience, strong wear resistance, simple preparation process, great reduction of development cost of the spray coating by taking industrial solid wastes as raw materials, and environmental friendliness.
In order to achieve the purpose, the technical scheme is as follows:
a preparation method of an aluminum-silicon wear-resistant spray coating for hot repair comprises the following steps:
1) adding waste electric porcelain particles and silica fume into a planetary type mixing machine according to the mass ratio of 100: 20-25, and mixing for 5-8 minutes to obtain a mixed particle material;
2) adding the obtained mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary mixing machine according to the mass ratio of 100: 5-8: 10-15: 15-20, and mixing for 10-12 minutes to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 6-8 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 8-10 wt% of the precursor mixture into the precursor mixture, stirring for 5-8 minutes, and sealing for ageing for 30-40 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 0.5-1.5 wt% of the mixture into the obtained mixture, and stirring for 5-8 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair.
According to the scheme, the granularity of the waste electric porcelain particles is 0.1-2 mm, and the volume density of the waste electric porcelain particles is 2.68-2.84 g/cm 3 8-10% of water absorption, Al 2 O 3 The content is 40~45wt%,SiO 2 The content is 45-50 wt%.
According to the scheme, the granularity of the rho-alumina is 80-100 mu m, and Al 2 O 3 The content is more than or equal to 98.5 wt%, and the true density is 3.4-3.6 g/cm 3
According to the scheme, the clay has the granularity of 50-60 mu m and Al 2 O 3 25 to 30 wt% of SiO 2 The content is 30-40 wt%, and the true density is 1.4-1.6 g/cm 3
According to the scheme, the sillimanite has the granularity of 40-50 mu m and Al 2 O 3 60-65 wt% of SiO 2 The content is 30-35 wt%, and the true density is 3.0-3.1 g/cm 3
According to the scheme, the particle size of the diatomite is 60-100 mu m, and Al is 2 O 3 3-5 wt% of SiO 2 The content is 85-88 wt%, and the true density is 0.6-0.8 g/cm 3
According to the scheme, the SiO of the chrysotile fiber 2 35-40 wt% of MgO, 40-45 wt% of Al 2 O 3 0.5 to 2 wt% of Fe 2 O 3 The content is less than or equal to 0.8 wt%, the diameter of the chrysotile fiber is 5-15 mu m, the length of the chrysotile fiber is 5-25 mm, and the volume weight of the chrysotile fiber is 0.4-0.6 g/cm 3
Compared with the prior art, the invention has the following beneficial effects:
the invention takes the industrial solid wastes such as waste electroceramics, silica fume and the like as raw materials, and reduces the preparation cost of the spray coating. The preparation process needs no special equipment or instrument and is simple.
The invention utilizes the oxidation of simple substance Si in the silica fume at high temperature and thermal state to form active SiO 2 The components improve the filling and sintering performance and promote the rapid sintering and integral forming of the spray coating.
The invention adopts cement-free combination, avoids the introduction of harmful components containing calcium and the like, and ensures the high-temperature thermal-state mechanical property of the spray coating.
The invention selects phosphate combination, and no harmful gas or liquid is generated in the preparation and service processes; the phosphate and the carboxymethyl cellulose are combined in a crosslinking manner, so that the binding performance of the spray coating is obviously improved, and the resilience of the spray coating is reduced.
According to the invention, a columnar mullite network staggered structure is formed through high-temperature secondary mullite reaction of sillimanite, so that the wear resistance of the spray coating is enhanced; simultaneously utilizes the volume expansion caused by the secondary mullite reaction to offset SiO 2 The volume shrinkage caused by the crystal transformation keeps the good volume stability of the spray paint.
According to the invention, the heat-conducting property of the spray coating is reduced by utilizing the accumulation and filling of the diatomite and the chrysotile fiber, so that the energy conservation and consumption reduction of the high-temperature industrial kiln are realized.
The main raw materials used in the invention are low in cost and easy to obtain, so that the resource utilization of industrial solid wastes is realized, and the environmental protection effect is obvious; the prepared wear-resistant spray coating has strong associativity, good sintering integrity with a lining body, less construction resilience and strong wear resistance, and can be applied to spray repair of a material returning device of a circulating fluidized bed boiler.
The aluminum-silicon wear-resistant spray coating for hot repair prepared by the invention is detected as follows: the resilience rate is 2.7-3.5%; the volume density of the sintered product is 2.43-2.68 g/cm at 1250℃ and 131 3 (ii) a The abrasion loss of the normal-temperature abrasion resistance test after 131 firing at 1250 ℃ is 2.4-3.3 cm 3
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention more apparent, the present invention is further described in detail with reference to the following embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.
The invention relates to a preparation method of an aluminum-silicon wear-resistant spray coating for hot repair, which comprises the following specific processes:
1) adding waste electric porcelain particles and silica fume into a planetary type mixing machine according to the mass ratio of 100: 20-25, and mixing for 5-8 minutes to obtain a mixed particle material;
2) adding the obtained mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary mixing machine according to the mass ratio of 100: 5-8: 10-15: 15-20, and mixing for 10-12 minutes to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 6-8 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 8-10 wt% of the precursor mixture into the precursor mixture, stirring for 5-8 minutes, and sealing for ageing for 30-40 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 0.5-1.5 wt% of the mixture into the obtained mixture, and stirring for 5-8 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair.
In order to avoid repetition, the materials related to the specific embodiment are uniformly described as follows, and are not described in the embodiment again:
the particle size of the waste electric porcelain particles is 0.1-2 mm, and the volume density of the waste electric porcelain particles is 2.68-2.84 g/cm 3 8-10% of water absorption, Al 2 O 3 40 to 45 wt% of SiO 2 The content is 45-50 wt%.
The particle size of the rho-alumina is 80-100 mu m, and Al 2 O 3 The content is more than or equal to 98.5 wt%, and the true density is 3.4-3.6 g/cm 3
The clay has a particle size of 50-60 mu m and Al 2 O 3 25-30 wt% of SiO 2 The content is 30-40 wt%, and the true density is 1.4-1.6 g/cm 3
The sillimanite has a particle size of 40-50 μm and Al 2 O 3 60 to 65 wt% of SiO 2 The content is 30-35 wt%, and the true density is 3.0-3.1 g/cm 3
The particle size of the diatomite is 60-100 mu m, and Al 2 O 3 3-5 wt% of SiO 2 The content is 85-88 wt%, and the true density is 0.6-0.8 g/cm 3
SiO of the chrysotile fiber 2 35-40 wt% of MgO, 40-45 wt% of Al 2 O 3 0.5 to 2 wt% of Fe 2 O 3 The content is less than or equal to 0.8 wt%, the diameter of the chrysotile fiber is 5-15 mu m, the length of the chrysotile fiber is 5-25 mm, and the volume weight of the chrysotile fiber is 0.4-0.6 g/cm 3
Example 1
1) Adding the waste electric porcelain particles and the silica fume into a planetary type mixing and refining machine according to the mass ratio of 100: 23, and mixing for 6 minutes to obtain mixed particles;
2) adding the mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary mixing machine for mixing for 10 minutes according to the mass ratio of 100: 5: 12: 13: 18 to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 6 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 8 wt% of the precursor mixture into the precursor mixture, stirring for 7 minutes, and sealing for ageing for 35 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 0.8 wt% of the mixture into the mixture, and stirring for 7 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair.
The aluminum-silicon wear-resistant spray paint for hot repair prepared in the embodiment is detected as follows: the rebound resilience is 2.8%; the volume density of the sintered body is 2.52g/cm at 1250℃ and 131 3 (ii) a The abrasion loss of the normal temperature abrasion resistance test after 131 sintering at 1250 ℃ is 2.7m 3
Example 2
1) Adding the waste electric porcelain particles and the silica fume into a planetary type mixing machine according to the mass ratio of 100: 22, and mixing for 5 minutes to obtain a mixed particle material;
2) adding the mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary type mixing machine for mixing for 12 minutes according to the mass ratio of 100: 8: 14: 13: 17 to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 7.5 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 8.5 wt% of the precursor mixture into the precursor mixture, stirring for 7 minutes, and sealing for ageing for 30 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 1.2 wt% of the mixture into the mixture, and stirring for 5 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair.
The aluminum-silicon wear-resistant spray coating for hot repair prepared in the embodiment is detected as follows: the rebound resilience is 3.3%; the volume density of the sintered body is 2.66g/cm at 1250℃ and 131 3 (ii) a Normal temperature abrasion resistance test after 1250 ℃ 131 firingThe abrasion loss was 2.4cm 3
Example 3
1) Adding the waste electric porcelain particles and the silica fume into a planetary type mixing machine according to the mass ratio of 100: 25, and mixing for 6 minutes to obtain mixed particles;
2) adding the mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary mixing machine for mixing for 11 minutes according to the mass ratio of 100: 6: 11: 13: 18 to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 7 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 9.5 wt% of the precursor mixture into the precursor mixture, stirring for 8 minutes, and sealing for ageing for 40 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 1.5 wt% of the mixture into the mixture, and stirring for 7 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair.
The aluminum-silicon wear-resistant spray paint for hot repair prepared in the embodiment is detected as follows: the rebound resilience is 3.1%; the volume density of the sintered body is 2.61g/cm at 1250℃ and 131 3 (ii) a The abrasion loss of the normal temperature abrasion resistance test after the roasting of 1250 ℃ at 131 ℃ is 2.8cm 3
Example 4
1) Adding the waste electric porcelain particles and the silica fume into a planetary type mixing machine according to the mass ratio of 100: 24, and mixing for 7 minutes to obtain mixed particles;
2) adding the mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary type mixing machine according to the mass ratio of 100: 8: 15: 12: 15, and mixing for 12 minutes to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 6 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 10 wt% of the precursor mixture into the precursor mixture, stirring for 5 minutes, and sealing for ageing for 30 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 0.6 wt% of the mixture into the mixture, and stirring for 8 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair.
The aluminum-silicon wear-resistant spray coating for hot repair prepared in the embodiment is detected as follows: go back toThe elastic rate is 2.9%; the volume density of the sintered body is 2.52g/cm at 1250℃ and 131 3 (ii) a The abrasion loss of the normal temperature abrasion resistance test after 131 burning at 1250 ℃ is 3.3cm 3
It should be noted that the above-mentioned embodiments are only preferred embodiments of the present invention, and the present invention is not limited thereto, and although the present invention has been described in detail with reference to the embodiments, it will be apparent to those skilled in the art that modifications can be made to the technical solutions described in the above-mentioned embodiments, or equivalent substitutions of some technical features, but any modifications, equivalents, improvements and the like within the spirit and principle of the present invention shall be included in the protection scope of the present invention.

Claims (5)

1. A preparation method of an aluminum-silicon wear-resistant spray coating for hot repair is characterized by comprising the following steps:
1) adding waste electric porcelain particles and silica fume into a planetary type mixing machine according to the mass ratio of 100: 20-25, and mixing for 5-8 minutes to obtain a mixed particle material;
2) adding the obtained mixed granular material, rho-alumina, clay, sillimanite and diatomite into a rotary mixing machine according to the mass ratio of 100: 5-8: 10-15: 15-20, and mixing for 10-12 minutes to obtain a precursor mixture;
3) sequentially adding chrysotile fibers accounting for 6-8 wt% of the precursor mixture and aluminum dihydrogen phosphate solution accounting for 8-10 wt% of the precursor mixture into the precursor mixture, stirring for 5-8 minutes, and sealing for ageing for 30-40 minutes to obtain a mixture;
4) adding carboxymethyl cellulose accounting for 0.5-1.5 wt% of the mixture into the obtained mixture, and stirring for 5-8 minutes to obtain the aluminum-silicon wear-resistant spray coating for thermal state repair;
the particle size of the waste electric porcelain particles is 0.1-2 mm, and the volume density of the waste electric porcelain particles is 2.68-2.84 g/cm 3 Water absorption of 8-10%, Al 2 O 3 40 to 45 wt% of SiO 2 The content is 45-50 wt%;
the sillimanite has a particle size of 40-50 μm and Al 2 O 3 Content (wt.)60 to 65 wt% of SiO 2 The content is 30-35 wt%, and the true density is 3.0-3.1 g/cm 3
2. The method for preparing the aluminum-silicon wear-resistant spray coating for hot patching as claimed in claim 1, wherein the particle size of the rho-alumina is 80-100 μm, and Al is 2 O 3 The content is more than or equal to 98.5 wt%, and the true density is 3.4-3.6 g/cm 3
3. The method for preparing the aluminum-silicon wear-resistant spray coating for thermal repair according to claim 1, wherein the clay has a particle size of 50 to 60 μm and Al 2 O 3 25 to 30 wt% of SiO 2 The content is 30-40 wt%, and the true density is 1.4-1.6 g/cm 3
4. The method for preparing the aluminum-silicon wear-resistant spray coating for thermal repair according to claim 1, wherein the diatomite has a particle size of 60-100 μm and Al 2 O 3 3-5 wt% of SiO 2 The content is 85-88 wt%, and the true density is 0.6-0.8 g/cm 3
5. The method for preparing the aluminum-silicon wear-resistant spray coating for hot patching as claimed in claim 1, wherein the SiO of the chrysotile fiber 2 35-40 wt% of MgO, 40-45 wt% of Al 2 O 3 0.5 to 2 wt% of Fe 2 O 3 The content is less than or equal to 0.8 wt%, the diameter of the chrysotile fiber is 5-15 mu m, the length of the chrysotile fiber is 5-25 mm, and the volume weight of the chrysotile fiber is 0.4-0.6 g/cm 3
CN202110937005.7A 2021-08-16 2021-08-16 Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair Active CN113788687B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110937005.7A CN113788687B (en) 2021-08-16 2021-08-16 Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110937005.7A CN113788687B (en) 2021-08-16 2021-08-16 Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair

Publications (2)

Publication Number Publication Date
CN113788687A CN113788687A (en) 2021-12-14
CN113788687B true CN113788687B (en) 2022-08-26

Family

ID=79181715

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110937005.7A Active CN113788687B (en) 2021-08-16 2021-08-16 Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair

Country Status (1)

Country Link
CN (1) CN113788687B (en)

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69804577T2 (en) * 1997-12-05 2002-10-17 Kawasaki Steel Co Material and process for repairing coke oven chambers
CN102060549B (en) * 2009-11-16 2013-07-03 中冶建筑研究总院有限公司 Low springback rate spraying and coating material for thermal-state blast furnace maintenance and preparation method thereof
CN103113120B (en) * 2011-11-17 2014-04-09 中冶武汉冶金建筑研究院有限公司 Phosphate-combined iron runner spraying paint for hot-state repairing
CN102701762B (en) * 2012-06-08 2013-12-11 武汉钢铁(集团)公司 Regeneration repairing material for blast-furnace casting runner and preparation method for regeneration repairing material
CN104496503B (en) * 2014-12-29 2017-12-12 通达耐火技术股份有限公司 A kind of Rapid-Repair refractory material and its preparation and application method
CN106242588A (en) * 2016-07-14 2016-12-21 武汉钢铁股份有限公司 Torpedo tank liner spray repair material for repairing and preparation method and application
CN108911641A (en) * 2018-08-31 2018-11-30 南京兴佑交通科技有限公司 A kind of mixture and its method for repairing and mending of fast repairing asphalt pavement
CN110041058B (en) * 2019-05-10 2022-01-25 武汉钢铁有限公司 Repairing material for coke oven lining
CN110627490B (en) * 2019-10-25 2022-02-01 中冶武汉冶金建筑研究院有限公司 Preparation method and application of environment-friendly self-flow aluminum-silicon refractory injection molding material
CN111018547B (en) * 2019-11-07 2022-01-28 浙江锦诚新材料股份有限公司 Light spray coating for blast furnace taphole smoke hood
CN111943693A (en) * 2020-07-20 2020-11-17 武汉钢铁有限公司 Torpedo tank lining smearing repairing material, preparation method and use method
CN112079608A (en) * 2020-09-15 2020-12-15 中冶武汉冶金建筑研究院有限公司 Self-flowing heat-resistant concrete using waste electric porcelain
CN112142448B (en) * 2020-09-30 2022-12-27 湖南湘钢瑞泰科技有限公司 Gunning mix for converter steel tapping hole and preparation method thereof

Also Published As

Publication number Publication date
CN113788687A (en) 2021-12-14

Similar Documents

Publication Publication Date Title
CN110436946B (en) Acid-resistant spray paint for high-temperature part of vault of hot blast stove
AU2011240485B2 (en) Filter used for filtering molten metal and preparation method thereof
CN105859314B (en) A kind of smelting molten steel equipment carbon containing gunning refractory and preparation method thereof
CN104788115A (en) Fireproof spraying coating for steel ladle working lining and preparation method of fireproof spraying coating
CN108033799B (en) Castable for semi-steel tank nozzle
WO2011088742A1 (en) High temperature abrasion resistant repairing paint and preparing method thereof
CN109824371A (en) A kind of gasification furnace work lining fire-proof spray coating and preparation method thereof
CN106995309A (en) Fire resisting liner body crack is squeegeeed material
CN103396129B (en) Light-weight hot-blast furnace pipeline spray paint and application method thereof
CN110981509B (en) Preparation method of low-cost low-water-demand siliceous heat supplementing material
US11926762B2 (en) High-temperature nano-composite coating and preparation method thereof, and small bag flexible packaging coating
CN113354425B (en) Acid-resistant spray paint suitable for spherical roof of hot blast stove
CN105272198A (en) High-temperature anti-corrosion coating material, and usage method and application thereof
CN113788687B (en) Preparation method of aluminum-silicon wear-resistant spray coating for thermal state repair
CN107840671B (en) Light heat-insulating coating for coke oven and construction process thereof
CN114195529B (en) High-strength magnesia refractory mortar for refining ladle
CN103387398B (en) Air heating furnace pipeline spray coating and using method thereof
CN110642611B (en) Refractory ramming mass for iron ladle of ferrosilicon electric furnace and preparation method thereof
CA2301039C (en) Cement-free refractory castable system for wet process pumping/spraying
CN103396130A (en) Hot-blast furnace pipeline spray paint and application method thereof
CN103626508A (en) Alkaline gunning mix for RH dip pipe
CN108706967A (en) A kind of forsterite brick and its production technology
CN116217221B (en) Preparation method of high-strength heat-insulating refractory mortar
CN110981473A (en) High-temperature kiln furniture protective coating and preparation method thereof
CN114634320B (en) Heat-resistant and wear-resistant concrete 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