CN111825434A - Environment-friendly Al2O3-SiC-Ti3SiC2Castable and preparation method thereof - Google Patents
Environment-friendly Al2O3-SiC-Ti3SiC2Castable and preparation method thereof Download PDFInfo
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- CN111825434A CN111825434A CN202010504607.9A CN202010504607A CN111825434A CN 111825434 A CN111825434 A CN 111825434A CN 202010504607 A CN202010504607 A CN 202010504607A CN 111825434 A CN111825434 A CN 111825434A
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- 238000002360 preparation method Methods 0.000 title claims abstract description 31
- 229910009817 Ti3SiC2 Inorganic materials 0.000 claims abstract description 122
- 239000000843 powder Substances 0.000 claims abstract description 55
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims abstract description 54
- 239000000463 material Substances 0.000 claims abstract description 40
- 229910052593 corundum Inorganic materials 0.000 claims abstract description 39
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 39
- 239000002245 particle Substances 0.000 claims abstract description 38
- 239000010431 corundum Substances 0.000 claims abstract description 33
- 239000002994 raw material Substances 0.000 claims abstract description 32
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 26
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims abstract description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 15
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical compound [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000004568 cement Substances 0.000 claims abstract description 11
- 238000002156 mixing Methods 0.000 claims abstract description 11
- 229920005646 polycarboxylate Polymers 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims description 19
- 238000003756 stirring Methods 0.000 claims description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 114
- 229910052742 iron Inorganic materials 0.000 abstract description 57
- 238000007254 oxidation reaction Methods 0.000 abstract description 36
- 230000003647 oxidation Effects 0.000 abstract description 34
- 239000002893 slag Substances 0.000 abstract description 24
- 239000010426 asphalt Substances 0.000 abstract description 20
- 238000000034 method Methods 0.000 abstract description 16
- 238000009991 scouring Methods 0.000 abstract description 13
- 230000008569 process Effects 0.000 abstract description 11
- 230000007797 corrosion Effects 0.000 abstract description 7
- 238000005260 corrosion Methods 0.000 abstract description 7
- 230000035699 permeability Effects 0.000 abstract description 5
- 230000004907 flux Effects 0.000 abstract description 4
- 230000007613 environmental effect Effects 0.000 abstract description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 238000005266 casting Methods 0.000 description 13
- 238000001816 cooling Methods 0.000 description 10
- 230000003628 erosive effect Effects 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 10
- 238000010079 rubber tapping Methods 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 6
- 229910001845 yogo sapphire Inorganic materials 0.000 description 6
- 230000035939 shock Effects 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 229910052681 coesite Inorganic materials 0.000 description 4
- 229910052906 cristobalite Inorganic materials 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229910052682 stishovite Inorganic materials 0.000 description 4
- 229910052905 tridymite Inorganic materials 0.000 description 4
- 238000003912 environmental pollution Methods 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000000779 smoke Substances 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- 238000003723 Smelting Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 230000008092 positive effect Effects 0.000 description 2
- 230000003313 weakening effect Effects 0.000 description 2
- 229910052580 B4C Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
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- 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
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
- C04B35/101—Refractories from grain sized mixtures
- C04B35/103—Refractories from grain sized mixtures containing non-oxide refractory materials, e.g. carbon
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/32—Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3217—Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
- C04B2235/3222—Aluminates other than alumino-silicates, e.g. spinel (MgAl2O4)
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/34—Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
- C04B2235/3427—Silicates other than clay, e.g. water glass
- C04B2235/3463—Alumino-silicates other than clay, e.g. mullite
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- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3826—Silicon carbides
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- C04B2235/02—Composition of constituents of the starting material or of secondary phases of the final product
- C04B2235/30—Constituents and secondary phases not being of a fibrous nature
- C04B2235/38—Non-oxide ceramic constituents or additives
- C04B2235/3817—Carbides
- C04B2235/3839—Refractory metal carbides
- C04B2235/3843—Titanium carbides
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- C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
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- C04B2235/9669—Resistance against chemicals, e.g. against molten glass or molten salts
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Abstract
The invention relates to environment-friendly Al2O3‑SiC‑Ti3SiC2A castable and a preparation method thereof. The technical scheme is as follows: environment-friendly Al2O3‑SiC‑Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-60 parts by mass of brown corundum particles, 15-20 parts by mass of silicon carbide particles, 25-35 parts by mass of silicon carbide fine powder or white corundum fine powder, 6-12 parts by mass of alumina micro powder or silica micro powder, and Ti3SiC26-10 parts of powder and 1-3 parts of calcium aluminate cement. Mixing the raw materials, adding polycarboxylate and water to prepare the environment-friendly Al2O3‑SiC‑Ti3SiC2And (5) pouring a material. The invention uses Ti3SiC2Replaces the traditional asphalt, has the characteristics of simple process and environmental protection, and the prepared environment-friendly Al2O3‑SiC‑Ti3SiC2Strong oxidation resistance of castable and molten iron scouring resistanceExcellent slag corrosion resistance/permeability and high iron flux.
Description
[ technical field ] A method for producing a semiconductor device
The invention belongs to the field of refractory castable for blast furnace tapping channels, and particularly relates to environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof.
[ background of the invention ]
The progress of the steel smelting technology promotes the large-scale development of the blast furnace, and the blast furnace smelting strength is increased continuously, the tapping temperature is gradually increased, and the molten iron flow is also increased obviously. At present, the tapping time of a large-scale blast furnace is prolonged, the tapping times are more frequent, and the flow rate of molten iron is accelerated, so that a tapping runner of the blast furnace faces long-time molten iron scouring and serious slag erosion. Therefore, the severe service environment of the large-scale blast furnace tapping channel puts higher requirements on the high-temperature mechanical property and the slag corrosion resistance of the tapping channel castable.
At present, the working lining of the blast furnace tapping channel is mainly made of Al2O3the-SiC-C castable is mainly made of Al and fully utilizes2O3The high thermal conductivity of silicon carbide and carbon in the-SiC-C castable and the non-wettability with iron slag endow the iron runner material with excellent scouring resistance, erosion resistance and thermal shock resistance. Generally, spherical asphalt is used as Al2O3A carbon source of the-SiC-C castable improves the slag corrosion resistance and the permeability of the iron runner castable. However, as is well known, the spherical asphalt is used as an activated carbon, the high-temperature oxidation temperature is about 700 ℃, asphalt on the surface of the castable is burnt out during the baking process of the iron runner castable, a porous iron runner working lining is remained, and Al is seriously reduced2O3Slag erosion/permeation resistance and molten iron scouring resistance of the-SiC-C castable. On the one hand, the oxidation loss of the spherical asphalt reduces Al2O3The non-wetting performance of the-SiC-C castable on the molten slag aggravates the erosion of the molten slag on the iron runner material; on the other hand, the burning loss of the asphalt damages the integrity of the iron runner material, reduces the surface strength of the castable material and aggravates the penetration of the iron slag into the castable material. Moreover, the burning loss of the asphalt in the baking process can release toxic smoke, which seriously affects the health of constructors and causes environmental pollution.
To solve the problem of Al2O3-SiC-C substanceThe patent technology of an erosion-resistant blast furnace iron runner self-flowing castable and a preparation method thereof (CN108503377A) discloses a castable of a composite antioxidant added with metal aluminum powder and boron carbide. The iron runner castable prepared by the method can improve the high-temperature oxidation resistance of the material through an antioxidant, but has limited oxidation resistance to spherical asphalt on the surface of the castable in the baking process (800 ℃ below zero). Furthermore, the patent technology of 'an iron runner castable containing modified graphite and a preparation method thereof' (CN201410738931.1) discloses a molten salt method for preparing the iron runner castable by modifying graphite and replacing spherical asphalt. The method adopts graphite as a carbon source to solve the problem of toxic gas generated by asphalt loss, but the graphite modification process is complex and is not suitable for industrial production, and the problem of poor oxidation resistance of the carbon source is still not solved by the modified graphite.
[ summary of the invention ]
The invention aims to overcome the defects of the prior art and aims to provide the environment-friendly Al with simple process2O3-SiC-Ti3SiC2Preparation method of castable and environment-friendly Al prepared by method2O3-SiC-Ti3SiC2The castable has strong oxidation resistance, molten iron scouring resistance, excellent slag erosion/permeability resistance and high iron flux.
In order to achieve the purpose, the technical scheme adopted by the invention comprises the following steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-60 parts by mass of brown corundum particles, 15-20 parts by mass of silicon carbide particles, 25-35 parts by mass of silicon carbide fine powder or white corundum fine powder, 6-12 parts by mass of alumina micro powder or silica micro powder, and Ti3SiC26-10 parts of powder and 1-3 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding into the mixtureAdding 0.5-1 wt% of polycarboxylate and 4-6 wt% of water, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
Al of the brown corundum particles2O3The content is more than or equal to 93 wt%; the particle size of the brown corundum particles is 3-8 mm.
The SiC content of the silicon carbide particles and the silicon carbide fine powder is more than or equal to 97 wt%; the granularity of the silicon carbide particles is 0-1 mm, and the granularity of the silicon carbide fine powder is less than or equal to 0.088 mm.
Al of the fine white corundum powder and the alumina micropowder2O3The content is more than or equal to 98 wt%; the granularity of the white corundum fine powder is less than or equal to 0.088mm, and the granularity of the alumina micro powder is less than or equal to 2 mu m.
The Ti3SiC2The purity of the powder is more than or equal to 99 wt%, and the granularity is less than or equal to 1 mu m.
Due to the adoption of the technical scheme, compared with the prior art, the invention has the following positive effects:
the invention adopts Ti3SiC2Replace the traditional Al2O3Spherical asphalt in-SiC-C castable to fully exert Ti3SiC2The asphalt has non-wettability and high oxidation resistance to iron slag, and solves the problem that the slag erosion resistance and molten iron scouring resistance of the iron runner castable are obviously reduced due to baking and oxidation of the traditional spherical asphalt. The invention is realized by directly adding Ti3SiC2Introducing into the casting material, and casting to obtain Al2O3-SiC-Ti3SiC2The iron runner material has simple process. As the prepared castable is not added with spherical asphalt, toxic smoke generated by asphalt oxidation of iron runner materials in the baking process and environmental pollution are not involved, the prepared Al2O3-SiC-Ti3SiC2The iron runner material is environment-friendly.
Ti3SiC2Being hexagonal, the crystal structure resembles the layered structure of the formation. This particular crystal structure imparts Ti3SiC2Excellent heat conducting performance, thermal shock resistance, damage tolerance resistance, high temperature oxidation resistance and melting propertyThe slag is not wettable. The invention is to mix Ti3SiC2The introduction into the iron runner castable is an effective way for taking the oxidation resistance, high-temperature slag corrosion resistance and molten iron scouring resistance of the iron runner into consideration. On the one hand, in Al2O3-SiC-Ti3SiC2The low-temperature ladle drying stage (800 ℃) of the castable is performed, and Ti is used3SiC2By means of the self oxidation resistance, the surface loosening phenomenon of the iron runner material caused by oxidation and burning loss of the traditional carbon source can be solved, and the weakening of the slag penetration resistance and the slag corrosion resistance of the iron runner material by the ladle drying process is avoided; on the other hand, Ti is added at the tapping stage (1500 ℃ C.) of the blast furnace3SiC2Can also be used as Al2O3-SiC-Ti3SiC2The high-efficiency antioxidant of the castable can be oxidized before SiC, so that the oxidization of SiC in the castable is thermodynamically hindered, and the molten iron scouring resistance of SiC in the castable is fully exerted. Notably, Ti3SiC2Oxidized in high temperature environment to form liquid TiO on the surface2And SiO2Due to liquid SiO2Has high viscosity, can not only fill pores in the casting material, but also effectively prevent oxygen from further flowing to Ti3SiC2Medium diffusion, kinetically preventing Al2O3-SiC-Ti3SiC2Oxidizing the casting material; further, Ti3SiC2Has high ductility at high temperature, and has a lamellar structure of Al2O3-SiC-Ti3SiC2The castable plays a two-dimensional toughening phase to toughen the castable and obviously improve Al2O3-SiC-Ti3SiC2High-temperature strength and thermal shock resistance of the casting material.
The invention prepares environment-friendly Al2O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 15-26 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 4-8 MPa, and the water cooling circulation times at 1100 ℃ are 8-12; the Al is2O3-SiC-Ti3SiC2Casting material is processed by the steps of 1The oxidation rate of SiC is 0.1-0.6 wt% after oxidation for 10 hours at 500 ℃; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 16-22 ten thousand tons.
Therefore, the invention has the characteristics of simple process and environmental protection, and the prepared environment-friendly Al2O3-SiC-Ti3SiC2The castable has strong oxidation resistance, molten iron scouring resistance, excellent slag erosion/permeability resistance and high iron flux.
The features and advantages of the present invention will be described in detail by way of examples.
[ detailed description ] embodiments
The invention is further described with reference to specific embodiments, without limiting its scope.
Al of the brown corundum particles2O3The content is more than or equal to 93 wt%; the particle size of the brown corundum particles is 3-8 mm.
The SiC content of the silicon carbide particles and the silicon carbide fine powder is more than or equal to 97 wt%; the granularity of the silicon carbide particles is 0-1 mm, and the granularity of the silicon carbide fine powder is less than or equal to 0.088 mm.
Al of the fine white corundum powder and the alumina micropowder2O3The content is more than or equal to 98 wt%; the granularity of the white corundum fine powder is less than or equal to 0.088mm, and the granularity of the alumina micro powder is less than or equal to 2 mu m.
The Ti3SiC2The purity of the powder is more than or equal to 99 wt%, and the granularity is less than or equal to 1 mu m.
Example 1
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-50 parts by mass of brown corundum particles, 18-20 parts by mass of silicon carbide particles, 15-24 parts by mass of silicon carbide fine powder, 8-16 parts by mass of white corundum fine powder, 4-8 parts by mass of alumina micro powder, 2-6 parts by mass of silica micro powder, and Ti3SiC2The powder accounts for 6-8 mass percent1-2.5 parts by mass of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4-5.5 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
Environment-friendly Al prepared in example 12O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 15-20 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 4-6 MPa, and the water cooling circulation times at 1100 ℃ are 8-10; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.3-0.6 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 16-18 ten thousand tons.
Example 2
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-50 parts by mass of brown corundum particles, 15-18 parts by mass of silicon carbide particles, 12-20 parts by mass of silicon carbide fine powder, 10-16 parts by mass of white corundum fine powder, 4-6 parts by mass of alumina micro powder, 2-7 parts by mass of silica micro powder, and Ti3SiC27-10 parts of powder and 2-3 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.6-0.9 wt% of polycarboxylate and 4-5 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
The true bookExample 2 preparation of Environment-friendly Al2O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 21-25 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 6-8 MPa, and the water cooling circulation times at 1100 ℃ are 10-12; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.1-0.4 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 20-22 ten thousand tons.
Example 3
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 50-60 parts by mass of brown corundum particles, 15-18 parts by mass of silicon carbide particles, 13-24 parts by mass of silicon carbide fine powder, 9-15 parts by mass of white corundum fine powder, 4-6 parts by mass of alumina micro powder, 2-7 parts by mass of silica micro powder, and Ti3SiC27-10 parts of powder and 1.5-3 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4.5-6 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
The environment-friendly Al prepared in this example 32O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 23-26 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 6-7.6 MPa, and the water cooling circulation times at 1100 ℃ are 9-12; the Al is2O3-SiC-Ti3SiC2The casting material is processed by 150 g in air atmosphereThe oxidation rate of SiC is 0.2 to 0.5 weight percent after the SiC is oxidized for 10 hours at the temperature of 0 ℃; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 19-20 ten thousand tons.
Example 4
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 50-60 parts by mass of brown corundum particles, 18-20 parts by mass of silicon carbide particles, 11-20 parts by mass of silicon carbide fine powder, 10-16 parts by mass of white corundum fine powder, 4-8 parts by mass of alumina micro powder, 2-6 parts by mass of silica micro powder, and Ti3SiC26-8 parts of powder and 1.5-2 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4-5.5 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
The environment-friendly Al prepared in this example 42O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 16-19 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 4.3-5.6 MPa, and the water cooling cycle times at 1100 ℃ are 8-9; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.3-0.6 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 16-19 ten thousand tons.
Example 5
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-50 parts by mass of brown corundum particles, 15-18 parts by mass of silicon carbide particles, 12-20 parts by mass of silicon carbide fine powder, 9-15 parts by mass of white corundum fine powder, 4-6 parts by mass of alumina micro powder, 2-7 parts by mass of silica micro powder, and Ti3SiC26-9 parts of powder and 1-2 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4-5 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
The environment-friendly Al prepared in this example 52O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 18-24 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 4.2-6.1 MPa, and the water cooling cycle times at 1100 ℃ are 8-10; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.2-0.6 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 17-20 ten thousand tons.
Example 6
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 50-60 parts by mass of brown corundum particles, 18-20 parts by mass of silicon carbide particles, 13-24 parts by mass of silicon carbide fine powder, 8-16 parts by mass of white corundum fine powder, 4-8 parts by mass of alumina micro powder, 2-6 parts by mass of silica micro powder, and Ti3SiC27-10 parts of powder and 1.5-2.5 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4.5-6 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
The environment-friendly Al prepared in this example 62O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 22-25 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 6.8-7.9 MPa, and the water cooling cycle times at 1100 ℃ are 9-11; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.1-0.4 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 18-21 ten thousand tons.
Example 7
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-50 parts by mass of brown corundum particles, 15-18 parts by mass of silicon carbide particles, 25-35 parts by mass of silicon carbide fine powder, 4-6 parts by mass of alumina micro powder, 2-7 parts by mass of silica micro powder, and Ti3SiC26-9 parts of powder and 1-2 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4-5 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
EXAMPLE 7 preparationIs environment-friendly Al2O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 16-21 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 4.2-5.7 MPa, and the water cooling circulation times at 1100 ℃ are 8-10; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.3-0.6 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 16-19 ten thousand tons.
Example 8
Environment-friendly Al2O3-SiC-Ti3SiC2A castable and a preparation method thereof. The preparation method of the embodiment comprises the following specific steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 50-60 parts by mass of brown corundum particles, 18-20 parts by mass of silicon carbide particles, 25-35 parts by mass of white corundum fine powder, 4-8 parts by mass of alumina micro powder, 2-6 parts by mass of silica micro powder, and Ti3SiC27-10 parts of powder and 1.5-2.5 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-0.8 wt% of polycarboxylate and 4.5-6 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a powerful stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
The environment-friendly Al prepared in this example 82O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 18-22 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 6-7.4 MPa, and the water cooling circulation times at 1100 ℃ are 8-10; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the casting material is 0.1-0 after the casting material is oxidized for 10 hours at 1500 ℃ in the air atmosphere.4 wt%; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 16-19 ten thousand tons.
Compared with the prior art, the specific implementation mode has the following positive effects:
this embodiment uses Ti3SiC2Replace the traditional Al2O3Spherical asphalt in-SiC-C castable to fully exert Ti3SiC2The asphalt has non-wettability and high oxidation resistance to iron slag, and solves the problem that the slag erosion resistance and molten iron scouring resistance of the iron runner castable are obviously reduced due to baking and oxidation of the traditional spherical asphalt. This embodiment is achieved by directly reacting Ti3SiC2Introducing into the casting material, and casting to obtain Al2O3-SiC-Ti3SiC2The iron runner material has simple process. As the prepared castable is not added with spherical asphalt, toxic smoke generated by asphalt oxidation of iron runner materials in the baking process and environmental pollution are not involved, the prepared Al2O3-SiC-Ti3SiC2The iron runner material is environment-friendly.
Ti3SiC2Being hexagonal, the crystal structure resembles the layered structure of the formation. This particular crystal structure imparts Ti3SiC2Excellent heat conducting performance, thermal shock resistance, damage tolerance resistance, high temperature oxidation resistance and non-wettability with slag. This embodiment is described with Ti3SiC2Introduced into Al2O3the-SiC castable is an effective way for taking the oxidation resistance, high-temperature slag corrosion resistance and molten iron scouring resistance of the iron runner material into consideration. On the one hand, in Al2O3-SiC-Ti3SiC2The low-temperature ladle drying stage (800 ℃) of the castable is performed, and Ti is used3SiC2By means of the self oxidation resistance, the surface loosening phenomenon of the iron runner material caused by oxidation and burning loss of the traditional carbon source can be solved, and the weakening of the slag penetration resistance and the slag corrosion resistance of the iron runner material by the ladle drying process is avoided; on the other hand, Ti is added at the tapping stage (1500 ℃ C.) of the blast furnace3SiC2Can also be used as Al2O3-SiC-Ti3SiC2The high-efficiency antioxidant of the castable can be oxidized before SiC, so that the oxidization of SiC in the castable is thermodynamically hindered, and the molten iron scouring resistance of SiC in the castable is fully exerted. Notably, Ti3SiC2Oxidized in high temperature environment to form liquid TiO on the surface2And SiO2Due to liquid SiO2Has high viscosity, can not only fill pores in the casting material, but also effectively prevent oxygen from further flowing to Ti3SiC2Medium diffusion, kinetically preventing Al2O3-SiC-Ti3SiC2Oxidizing the casting material; further, Ti3SiC2Has high ductility at high temperature, and has a lamellar structure of Al2O3-SiC-Ti3SiC2The castable plays a two-dimensional toughening phase to toughen the castable and obviously improve Al2O3-SiC-Ti3SiC2Thermal shock resistance of the castable.
The environment-friendly Al prepared by the specific embodiment2O3-SiC-Ti3SiC2And (3) detecting a sintered sample after the castable is subjected to heat treatment at 1450 ℃ for 3 hours in an air atmosphere: the normal-temperature breaking strength of the sample is 15-26 MPa, the high-temperature breaking strength (1450 ℃ multiplied by 0.5h) is 4-8 MPa, and the water cooling circulation times at 1100 ℃ are 8-12; the Al is2O3-SiC-Ti3SiC2The SiC oxidation rate of the castable is 0.1-0.6 wt% after the castable is oxidized for 10 hours at 1500 ℃ in the air atmosphere; the Al is2O3-SiC-Ti3SiC2The iron feeding amount of the castable is 16-22 ten thousand tons.
Therefore, the specific implementation mode has the characteristics of simple process and environmental friendliness, and the prepared environment-friendly Al2O3-SiC-Ti3SiC2The castable has strong oxidation resistance, molten iron scouring resistance, excellent slag erosion/permeability resistance and high iron flux.
The above embodiments are illustrative of the present invention, and are not intended to limit the present invention, and any simple modifications of the present invention are within the scope of the present invention.
Claims (6)
1. Environment-friendly Al2O3-SiC-Ti3SiC2The preparation method of the castable is characterized by comprising the following steps: the preparation method comprises the following steps:
step one, environment-friendly Al2O3-SiC-Ti3SiC2The castable comprises the following raw material components in percentage by weight: 40-60 parts by mass of brown corundum particles, 15-20 parts by mass of silicon carbide particles, 25-35 parts by mass of silicon carbide fine powder or white corundum fine powder, 6-12 parts by mass of alumina micro powder or silica micro powder, and Ti3SiC26-10 parts of powder and 1-3 parts of calcium aluminate cement;
step two, mixing the raw materials according to the raw material components and the content thereof to obtain a mixture; adding 0.5-1 wt% of polycarboxylate and 4-6 wt% of water into the mixture, and uniformly stirring for 20-30 min by using a stirrer to obtain the environment-friendly Al2O3-SiC-Ti3SiC2And (5) pouring a material.
2. The environment-friendly Al of claim 12O3-SiC-Ti3SiC2The preparation method of the castable is characterized in that the Al of the brown corundum particles2O3The content is more than or equal to 93 wt%; the particle size of the brown corundum particles is 3-8 mm.
3. The environment-friendly Al of claim 12O3-SiC-Ti3SiC2The preparation method of the castable is characterized in that the SiC content of the silicon carbide particles and the silicon carbide fine powder is more than or equal to 97 wt%; the granularity of the silicon carbide particles is 0-1 mm, and the granularity of the silicon carbide fine powder is less than or equal to 0.088 mm.
4. The environment-friendly Al of claim 12O3-SiC-Ti3SiC2The preparation method of the castable is characterized in that the white corundum fine powder and the Al of the alumina micropowder2O3The content is more than or equal to 98 wt%; the granularity of the white corundum fine powder is less than or equal to 0.088mm, and the granularity of the alumina micro powder is less than or equal to 0.088mmThe particle size is less than or equal to 2 mu m.
5. The environment-friendly Al of claim 12O3-SiC-Ti3SiC2The preparation method of the castable is characterized in that the Ti is3SiC2The purity of the powder is more than or equal to 99 wt%, and the granularity is less than or equal to 1 mu m.
6. Environment-friendly Al2O3-SiC-Ti3SiC2The castable is characterized in that: the environment-friendly Al2O3-SiC-Ti3SiC2The castable is the environment-friendly Al according to any one of claims 1-52O3-SiC-Ti3SiC2Environment-friendly Al prepared by preparation method of castable2O3-SiC-Ti3SiC2And (5) pouring a material.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113999027A (en) * | 2021-11-12 | 2022-02-01 | 湖南立达高新材料有限公司 | Corundum-mullite castable for zinc oxide rotary kiln and preparation method thereof |
CN117776690A (en) * | 2024-02-27 | 2024-03-29 | 北京利尔高温材料股份有限公司 | Sol-combined blast furnace iron runner gunning material |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005281084A (en) * | 2004-03-30 | 2005-10-13 | Tungaloy Corp | Sintered compact and manufacturing method therefor |
CN101898897A (en) * | 2010-08-22 | 2010-12-01 | 卿如民 | Quick-drying self-flow iron runner castable material and application method thereof |
CN102603274A (en) * | 2012-04-06 | 2012-07-25 | 武汉科技大学 | Cramp iron castable and preparation method thereof |
CN102992795A (en) * | 2013-01-07 | 2013-03-27 | 中钢集团洛阳耐火材料研究院有限公司 | Environment-friendly castable for blast furnace iron runners |
CN106715359A (en) * | 2014-12-02 | 2017-05-24 | 里弗雷克特里知识产权两合公司 | Refractory product, batch composition for producing said product, method for producing the product and use of said product |
CN108516849A (en) * | 2018-06-06 | 2018-09-11 | 武汉科技大学 | A kind of cement kiln Zircon mullite brick and preparation method thereof |
CN108602723A (en) * | 2016-03-08 | 2018-09-28 | 里弗雷克特里知识产权两合公司 | Refractory ceramic product |
CN109293347A (en) * | 2018-10-12 | 2019-02-01 | 湖南立达高新材料有限公司 | A kind of mineral hot furnace tapping hole environmentally protective stemming and preparation method thereof |
CN110183238A (en) * | 2019-05-30 | 2019-08-30 | 惠世军 | A kind of preparation method of anti-oxidant resistance to thermal shock type nozzle brick |
-
2020
- 2020-06-05 CN CN202010504607.9A patent/CN111825434A/en active Pending
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005281084A (en) * | 2004-03-30 | 2005-10-13 | Tungaloy Corp | Sintered compact and manufacturing method therefor |
CN101898897A (en) * | 2010-08-22 | 2010-12-01 | 卿如民 | Quick-drying self-flow iron runner castable material and application method thereof |
CN102603274A (en) * | 2012-04-06 | 2012-07-25 | 武汉科技大学 | Cramp iron castable and preparation method thereof |
CN102992795A (en) * | 2013-01-07 | 2013-03-27 | 中钢集团洛阳耐火材料研究院有限公司 | Environment-friendly castable for blast furnace iron runners |
CN106715359A (en) * | 2014-12-02 | 2017-05-24 | 里弗雷克特里知识产权两合公司 | Refractory product, batch composition for producing said product, method for producing the product and use of said product |
CN108602723A (en) * | 2016-03-08 | 2018-09-28 | 里弗雷克特里知识产权两合公司 | Refractory ceramic product |
CN108516849A (en) * | 2018-06-06 | 2018-09-11 | 武汉科技大学 | A kind of cement kiln Zircon mullite brick and preparation method thereof |
CN109293347A (en) * | 2018-10-12 | 2019-02-01 | 湖南立达高新材料有限公司 | A kind of mineral hot furnace tapping hole environmentally protective stemming and preparation method thereof |
CN110183238A (en) * | 2019-05-30 | 2019-08-30 | 惠世军 | A kind of preparation method of anti-oxidant resistance to thermal shock type nozzle brick |
Non-Patent Citations (1)
Title |
---|
中国有色金属工业协会: "耐火材料新工艺技术 第2版", 中国建材工业出版社, pages: 188 - 189 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113999027A (en) * | 2021-11-12 | 2022-02-01 | 湖南立达高新材料有限公司 | Corundum-mullite castable for zinc oxide rotary kiln and preparation method thereof |
CN117776690A (en) * | 2024-02-27 | 2024-03-29 | 北京利尔高温材料股份有限公司 | Sol-combined blast furnace iron runner gunning material |
CN117776690B (en) * | 2024-02-27 | 2024-05-31 | 北京利尔高温材料股份有限公司 | Sol-combined blast furnace iron runner gunning material |
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